Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 25782 |
|---|---|
| ensemblid | ENSG00000118873.17 |
| hgncid | 17168 |
| symbol | RAB3GAP2 |
| name | RAB3 GTPase activating non-catalytic protein subunit 2 |
| refseq_nuc | NM_012414.4 |
| refseq_prot | NP_036546.2 |
| ensembl_nuc | ENST00000358951.7 |
| ensembl_prot | ENSP00000351832.2 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 220148293 |
| end | 220272453 |
| strand | - |
| ver | v1.2 |
| region | chr1:220148293-220272453 |
| region5000 | chr1:220143293-220277453 |
| regionname0 | RAB3GAP2_chr1_220148293_220272453 |
| regionname5000 | RAB3GAP2_chr1_220143293_220277453 |
| 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 | 1393 | 323 | 81 | 57 | 148 | 7 | 28 | 118 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0002 | 0/0 | 1393 | 25 | 1 | 5 | 11 | 1 | 7 | 9 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0003 | 0/0 | 1393 | 19 | 5 | 2 | 10 | 0 | 2 | 6 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0004 | 0/0 | 1393 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0005 | 0/0 | 1393 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0006 | 0/0 | 1393 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0007 | 0/0 | 1393 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0008 | 0/0 | 1393 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0009 | 0/0 | 1393 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0010 | 0/0 | 1393 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0011 | 0/0 | 84 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0012 | 0/0 | 1393 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0013 | 0/0 | 1393 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| 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 | 4182 | 310 | 70 | 56 | 147 | 7 | 28 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| c0002 | 0/0 | 4182 | 24 | 1 | 5 | 10 | 1 | 7 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| c0003 | 0/0 | 4182 | 18 | 4 | 2 | 10 | 0 | 2 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| c0004 | 0/0 | 4182 | 8 | 7 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| c0005 | 0/0 | 4182 | 2 | 0 | 0 | 0 | 0 | 2 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| c0006 | 0/0 | 4182 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| c0007 | 0/0 | 4182 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| c0008 | 0/0 | 4182 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| c0009 | 0/0 | 4182 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| c0010 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| c0011 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| c0012 | 0/0 | 4182 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| c0013 | 0/0 | 4182 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| c0014 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| c0015 | 0/0 | 4182 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| c0016 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| c0017 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| c0018 | 0/0 | 4182 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| c0019 | 0/0 | 4166 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| c0020 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| c0021 | 0/0 | 4182 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| 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 | 1/1 | 3075 | 94 | 22 | 22 | 34 | 3 | 11 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0002 | 0/0 | 3074 | 81 | 18 | 14 | 40 | 4 | 5 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0003 | 0/0 | 3071 | 47 | 4 | 3 | 38 | 0 | 2 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0004 | 0/0 | 3073 | 45 | 11 | 5 | 28 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0005 | 0/0 | 3078 | 17 | 0 | 3 | 8 | 0 | 6 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0006 | 0/0 | 3073 | 17 | 3 | 2 | 8 | 0 | 4 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0007 | 0/0 | 3075 | 15 | 1 | 5 | 4 | 1 | 4 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0008 | 0/0 | 3074 | 12 | 0 | 1 | 8 | 0 | 3 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0009 | 0/0 | 3074 | 12 | 12 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0010 | 0/0 | 3075 | 4 | 0 | 3 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0011 | 0/0 | 3076 | 3 | 1 | 1 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0012 | 0/0 | 3072 | 3 | 1 | 0 | 1 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0013 | 0/0 | 3075 | 3 | 3 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0014 | 0/0 | 3075 | 2 | 2 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0015 | 0/0 | 3074 | 2 | 1 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0016 | 0/0 | 3070 | 2 | 0 | 0 | 1 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0017 | 0/0 | 3073 | 2 | 2 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0018 | 0/0 | 3075 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0019 | 0/0 | 3073 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0020 | 0/0 | 3072 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0021 | 0/0 | 3076 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0022 | 0/0 | 3075 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0023 | 0/0 | 3077 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0024 | 0/0 | 3074 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0025 | 0/0 | 3061 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0026 | 0/0 | 3074 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0027 | 0/0 | 3074 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0028 | 0/0 | 3074 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0029 | 0/0 | 3075 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0030 | 0/0 | 3074 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0031 | 0/0 | 3073 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0032 | 0/0 | 3070 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0033 | 0/0 | 3073 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| t0034 | 0/0 | 3074 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| 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 | 3 | 0 | 0 | 3 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0125 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0149 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| 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 | 4182 | 310 | 70 | 56 | 147 | 7 | 28 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0004 | 0/0 | 4182 | 8 | 7 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0011 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0012 | 0/0 | 4182 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0014 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0017 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0020 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0002c0002 | 0/0 | 4182 | 24 | 1 | 5 | 10 | 1 | 7 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0002c0007 | 0/0 | 4182 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0003c0003 | 0/0 | 4182 | 18 | 4 | 2 | 10 | 0 | 2 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0003c0016 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0004c0005 | 0/0 | 4182 | 2 | 0 | 0 | 0 | 0 | 2 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0005c0009 | 0/0 | 4182 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0006c0010 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0007c0013 | 0/0 | 4182 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0008c0015 | 0/0 | 4182 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0009c0008 | 0/0 | 4182 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0010c0018 | 0/0 | 4182 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0011c0019 | 0/0 | 4166 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0012c0006 | 0/0 | 4182 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0013c0021 | 0/0 | 4182 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 7256 | 85 | 18 | 22 | 30 | 3 | 10 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0002 | 0/0 | 7255 | 74 | 16 | 13 | 38 | 4 | 3 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0003 | 0/0 | 7252 | 43 | 4 | 3 | 34 | 0 | 2 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0004 | 0/0 | 7254 | 45 | 11 | 5 | 28 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0005 | 0/0 | 7259 | 16 | 0 | 3 | 7 | 0 | 6 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0006 | 0/0 | 7254 | 3 | 0 | 0 | 1 | 0 | 2 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0007 | 0/0 | 7256 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0008 | 0/0 | 7255 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0009 | 0/0 | 7255 | 4 | 4 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0010 | 0/0 | 7256 | 4 | 0 | 3 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0011 | 0/0 | 7257 | 3 | 1 | 1 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0012 | 0/0 | 7253 | 3 | 1 | 0 | 1 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0013 | 0/0 | 7256 | 3 | 3 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0014 | 0/0 | 7256 | 2 | 2 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0015 | 0/0 | 7255 | 2 | 1 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0016 | 0/0 | 7251 | 2 | 0 | 0 | 1 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0017 | 0/0 | 7254 | 2 | 2 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0018 | 0/0 | 7256 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0019 | 0/0 | 7254 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0020 | 0/0 | 7253 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0021 | 0/0 | 7257 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0022 | 0/0 | 7256 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0023 | 0/0 | 7258 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0024 | 0/0 | 7255 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0025 | 0/0 | 7242 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0026 | 0/0 | 7255 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0027 | 0/0 | 7255 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0028 | 0/0 | 7255 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0029 | 0/0 | 7256 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0030 | 0/0 | 7255 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0031 | 0/0 | 7254 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0032 | 0/0 | 7251 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0033 | 0/0 | 7254 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0001t0034 | 0/0 | 7255 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0004t0002 | 0/0 | 7255 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0004t0009 | 0/0 | 7255 | 7 | 7 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0011t0001 | 0/0 | 7256 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0012t0001 | 0/0 | 7256 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0014t0001 | 0/0 | 7256 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0017t0001 | 0/0 | 7256 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0001c0020t0009 | 0/0 | 7255 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0002c0002t0007 | 0/0 | 7256 | 14 | 1 | 4 | 4 | 1 | 4 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0002c0002t0008 | 0/0 | 7255 | 10 | 0 | 1 | 6 | 0 | 3 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0002c0007t0008 | 0/0 | 7255 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0003c0003t0002 | 0/0 | 7255 | 4 | 2 | 0 | 2 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0003c0003t0003 | 0/0 | 7252 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0003c0003t0006 | 0/0 | 7254 | 13 | 2 | 2 | 7 | 0 | 2 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0003c0016t0006 | 0/0 | 7254 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0004c0005t0002 | 0/0 | 7255 | 2 | 0 | 0 | 0 | 0 | 2 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0005c0009t0001 | 0/0 | 7256 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0006c0010t0001 | 0/0 | 7256 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0007c0013t0001 | 0/0 | 7256 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0008c0015t0005 | 0/0 | 7259 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0009c0008t0001 | 0/0 | 7256 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0010c0018t0003 | 0/0 | 7252 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0011c0019t0003 | 0/0 | 7236 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0012c0006t0003 | 0/0 | 7252 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| a0013c0021t0001 | 0/0 | 7256 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | copy fasta | chr1 | 220143293 | 220277453 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0125 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0149 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0003g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0004g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0005g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0005g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0005g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0005g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0005g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0005g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0005g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0005g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0005g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0005g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0005g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0005g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0006g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0006g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0006g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0007g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0008g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0009g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0009g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0009g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0009g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0010g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0010g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0010g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0010g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0011g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0011g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0011g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0012g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0012g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0012g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0013g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0013g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0013g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0014g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0014g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0015g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0015g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0016g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0016g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0017g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0017g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0018g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0019g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0020g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0021g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0022g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0023g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0024g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0025g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0026g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0027g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0028g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0029g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0030g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0031g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0032g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0033g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0001t0034g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0004t0002g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0004t0009g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0004t0009g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0004t0009g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0004t0009g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0004t0009g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0004t0009g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0011t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0012t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0014t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0017t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0001c0020t0009g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0002c0002t0007g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0002c0002t0007g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0002c0002t0007g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0002c0002t0007g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0002c0002t0007g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0002c0002t0007g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0002c0002t0007g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0002c0002t0007g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0002c0002t0007g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0002c0002t0007g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0002c0002t0007g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0002c0002t0007g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0002c0002t0008g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0002c0002t0008g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0002c0002t0008g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0002c0002t0008g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0002c0002t0008g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0002c0002t0008g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0002c0002t0008g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0002c0007t0008g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0003c0003t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0003c0003t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0003c0003t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0003c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0003c0003t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0003c0003t0006g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0003c0003t0006g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0003c0003t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0003c0003t0006g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0003c0003t0006g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0003c0003t0006g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0003c0003t0006g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0003c0003t0006g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0003c0003t0006g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0003c0003t0006g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0003c0003t0006g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0003c0003t0006g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0003c0003t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0003c0016t0006g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0004c0005t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0004c0005t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0005c0009t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0006c0010t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0007c0013t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0008c0015t0005g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0009c0008t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0010c0018t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0011c0019t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0012c0006t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| a0013c0021t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0119 | EUR | GBR | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0300 | EUR | GBR | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG00408 | hp1 | a0001 | c0001 | t0006 | g0364 | EAS | CHS | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | CHS | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG00423 | hp1 | a0002 | c0002 | t0007 | g0022 | EAS | CHS | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0259 | EAS | CHS | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | CHS | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG00544 | hp2 | a0001 | c0001 | t0032 | g0268 | EAS | CHS | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG00558 | hp1 | a0002 | c0007 | t0008 | g0018 | EAS | CHS | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | CHS | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0260 | EAS | CHS | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG00609 | hp1 | a0001 | c0001 | t0005 | g0138 | EAS | CHS | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG00609 | hp2 | a0003 | c0003 | t0006 | g0046 | EAS | CHS | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG00621 | hp1 | a0003 | c0003 | t0006 | g0058 | EAS | CHS | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG00639 | hp1 | a0002 | c0002 | t0008 | g0014 | AMR | PUR | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG00642 | hp1 | a0001 | c0001 | t0029 | g0117 | AMR | PUR | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0301 | AMR | PUR | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG00673 | hp1 | a0003 | c0003 | t0006 | g0049 | EAS | CHS | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | CHS | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG00735 | hp1 | a0001 | c0001 | t0033 | g0255 | AMR | PUR | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0315 | AMR | PUR | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0358 | AMR | PUR | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0359 | AMR | PUR | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01074 | hp2 | a0002 | c0002 | t0007 | g0009 | AMR | PUR | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01081 | hp1 | a0001 | c0001 | t0005 | g0152 | AMR | PUR | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0279 | AMR | PUR | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0276 | AMR | PUR | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01243 | hp1 | a0001 | c0001 | t0019 | g0262 | AMR | PUR | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01243 | hp2 | a0001 | c0001 | t0011 | g0351 | AMR | PUR | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01256 | hp2 | a0002 | c0002 | t0007 | g0016 | AMR | CLM | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01258 | hp1 | a0001 | c0001 | t0010 | g0106 | AMR | CLM | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01258 | hp2 | a0002 | c0002 | t0007 | g0017 | AMR | CLM | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01261 | hp2 | a0001 | c0001 | t0015 | g0340 | AMR | CLM | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0186 | AMR | CLM | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0329 | AMR | CLM | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0297 | AMR | CLM | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01361 | hp1 | a0003 | c0003 | t0006 | g0051 | AMR | CLM | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01433 | hp1 | a0001 | c0004 | t0002 | g0345 | AMR | CLM | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0099 | AMR | CLM | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01496 | hp2 | a0001 | c0001 | t0007 | g0115 | AMR | CLM | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0277 | EUR | IBS | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0128 | EUR | IBS | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01884 | hp1 | a0003 | c0003 | t0002 | g0043 | AFR | ACB | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01884 | hp2 | a0001 | c0001 | t0009 | g0343 | AFR | ACB | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01891 | hp1 | a0001 | c0001 | t0017 | g0216 | AFR | ACB | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01891 | hp2 | a0001 | c0001 | t0014 | g0210 | AFR | ACB | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01934 | hp1 | a0001 | c0001 | t0010 | g0105 | AMR | PEL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0313 | AMR | PEL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0323 | AMR | PEL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0306 | AMR | PEL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PEL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0331 | AMR | PEL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0326 | AMR | PEL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02004 | hp1 | a0001 | c0001 | t0010 | g0103 | AMR | PEL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02004 | hp2 | a0003 | c0003 | t0006 | g0041 | AMR | PEL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0253 | EAS | KHV | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0236 | EAS | KHV | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02040 | hp2 | a0001 | c0001 | t0016 | g0173 | EAS | KHV | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02055 | hp1 | a0001 | c0004 | t0009 | g0223 | AFR | ACB | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02055 | hp2 | a0001 | c0001 | t0024 | g0222 | AFR | ACB | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | KHV | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | KHV | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | KHV | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0240 | EAS | KHV | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02145 | hp1 | a0001 | c0011 | t0001 | g0156 | AFR | ACB | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | ACB | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0355 | AMR | PEL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0294 | AMR | PEL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | CDX | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0258 | EAS | CDX | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02165 | hp1 | a0001 | c0001 | t0020 | g0170 | EAS | CDX | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02165 | hp2 | a0003 | c0003 | t0006 | g0056 | EAS | CDX | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0350 | AFR | ACB | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0197 | AMR | PEL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0328 | AMR | PEL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PEL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02300 | hp1 | a0001 | c0001 | t0021 | g0104 | AMR | PEL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0318 | AMR | PEL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0334 | EAS | KHV | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | KHV | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02572 | hp1 | a0001 | c0001 | t0017 | g0217 | AFR | GWD | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02572 | hp2 | a0001 | c0020 | t0009 | g0368 | AFR | GWD | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02602 | hp1 | a0001 | c0001 | t0006 | g0274 | SAS | PJL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02615 | hp1 | a0003 | c0003 | t0002 | g0037 | AFR | GWD | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | GWD | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02622 | hp2 | a0001 | c0001 | t0014 | g0246 | AFR | GWD | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02630 | hp1 | a0001 | c0001 | t0015 | g0339 | AFR | GWD | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | GWD | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02698 | hp2 | a0002 | c0002 | t0007 | g0011 | SAS | PJL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0266 | AFR | GWD | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02717 | hp2 | a0001 | c0004 | t0009 | g0007 | AFR | GWD | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0237 | AFR | GWD | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02723 | hp2 | a0001 | c0001 | t0013 | g0219 | AFR | GWD | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02735 | hp1 | a0001 | c0001 | t0016 | g0208 | SAS | PJL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0108 | SAS | PJL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0171 | SAS | PJL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0317 | SAS | PJL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02809 | hp1 | a0001 | c0001 | t0030 | g0348 | AFR | GWD | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02818 | hp1 | a0001 | c0001 | t0011 | g0352 | AFR | GWD | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02818 | hp2 | a0001 | c0001 | t0009 | g0344 | AFR | GWD | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02886 | hp2 | a0003 | c0003 | t0006 | g0042 | AFR | GWD | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02896 | hp2 | a0001 | c0004 | t0009 | g0338 | AFR | GWD | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0029 | AFR | ESN | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0238 | AFR | ESN | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02976 | hp1 | a0001 | c0001 | t0013 | g0221 | AFR | ESN | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0035 | AFR | ESN | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03017 | hp2 | a0001 | c0001 | t0012 | g0174 | SAS | PJL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03041 | hp2 | a0001 | c0001 | t0034 | g0370 | AFR | GWD | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03098 | hp1 | a0006 | c0010 | t0001 | g0095 | AFR | MSL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03098 | hp2 | a0001 | c0004 | t0009 | g0342 | AFR | MSL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03130 | hp1 | a0001 | c0017 | t0001 | g0234 | AFR | ESN | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0212 | AFR | ESN | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0239 | AFR | ESN | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0034 | AFR | ESN | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03195 | hp2 | a0001 | c0004 | t0009 | g0063 | AFR | ESN | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | MSL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03209 | hp2 | a0001 | c0014 | t0001 | g0269 | AFR | MSL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | MSL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0225 | SAS | PJL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0218 | AFR | MSL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | MSL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03486 | hp1 | a0001 | c0001 | t0012 | g0267 | AFR | MSL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03491 | hp1 | a0002 | c0002 | t0007 | g0015 | SAS | PJL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03491 | hp2 | a0001 | c0001 | t0005 | g0356 | SAS | PJL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03492 | hp2 | a0002 | c0002 | t0007 | g0002 | SAS | PJL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03540 | hp2 | a0001 | c0004 | t0009 | g0007 | AFR | GWD | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03579 | hp1 | a0001 | c0004 | t0009 | g0349 | AFR | MSL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03579 | hp2 | a0001 | c0001 | t0028 | g0264 | AFR | MSL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03654 | hp1 | a0002 | c0002 | t0007 | g0012 | SAS | PJL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03654 | hp2 | a0003 | c0003 | t0006 | g0050 | SAS | PJL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03669 | hp1 | a0004 | c0005 | t0002 | g0295 | SAS | PJL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | STU | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03688 | hp2 | a0002 | c0002 | t0008 | g0354 | SAS | STU | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0096 | SAS | PJL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03704 | hp2 | a0001 | c0001 | t0005 | g0250 | SAS | PJL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03710 | hp1 | a0007 | c0013 | t0001 | g0150 | SAS | PJL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0353 | SAS | PJL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0296 | SAS | BEB | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0154 | SAS | BEB | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03834 | hp1 | a0001 | c0001 | t0031 | g0257 | SAS | BEB | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0316 | SAS | BEB | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03927 | hp1 | a0002 | c0002 | t0008 | g0021 | SAS | BEB | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03927 | hp2 | a0003 | c0003 | t0006 | g0052 | SAS | BEB | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG04115 | hp1 | a0004 | c0005 | t0002 | g0299 | SAS | STU | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG04115 | hp2 | a0001 | c0001 | t0011 | g0081 | SAS | STU | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG04184 | hp1 | a0002 | c0002 | t0008 | g0020 | SAS | BEB | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0195 | SAS | BEB | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0110 | SAS | STU | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | STU | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | STU | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG04228 | hp2 | a0001 | c0001 | t0005 | g0249 | SAS | STU | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18522 | hp1 | a0003 | c0003 | t0006 | g0038 | AFR | YRI | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0265 | AFR | YRI | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | CHB | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0230 | EAS | CHB | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | CHB | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | CHB | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | YRI | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0213 | AFR | YRI | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18942 | hp1 | a0002 | c0002 | t0008 | g0001 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18942 | hp2 | a0008 | c0015 | t0005 | g0140 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18943 | hp1 | a0001 | c0001 | t0010 | g0102 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18944 | hp2 | a0001 | c0001 | t0018 | g0073 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0252 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18952 | hp2 | a0003 | c0003 | t0002 | g0053 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18953 | hp1 | a0001 | c0001 | t0023 | g0141 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18953 | hp2 | a0010 | c0018 | t0003 | g0207 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18954 | hp1 | a0002 | c0002 | t0007 | g0023 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0251 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18961 | hp2 | a0005 | c0009 | t0001 | g0165 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0139 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0322 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18966 | hp1 | a0003 | c0003 | t0006 | g0045 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18967 | hp1 | a0001 | c0001 | t0004 | g0367 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18968 | hp2 | a0001 | c0001 | t0025 | g0135 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0321 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18969 | hp2 | a0003 | c0003 | t0006 | g0048 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0332 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0093 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18973 | hp1 | a0002 | c0002 | t0008 | g0003 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0333 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0362 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18978 | hp2 | a0001 | c0001 | t0004 | g0248 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18979 | hp1 | a0001 | c0001 | t0012 | g0314 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18980 | hp1 | a0001 | c0001 | t0004 | g0231 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0136 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0360 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18986 | hp1 | a0013 | c0021 | t0001 | g0369 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0324 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18988 | hp2 | a0001 | c0001 | t0005 | g0137 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0366 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18993 | hp1 | a0002 | c0002 | t0007 | g0004 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18994 | hp1 | a0001 | c0001 | t0005 | g0142 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18994 | hp2 | a0002 | c0002 | t0008 | g0001 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19001 | hp1 | a0001 | c0001 | t0005 | g0097 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0357 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0229 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19003 | hp1 | a0003 | c0003 | t0003 | g0057 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0330 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19005 | hp1 | a0012 | c0006 | t0003 | g0008 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19005 | hp2 | a0003 | c0003 | t0002 | g0054 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0336 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19009 | hp1 | a0001 | c0001 | t0005 | g0155 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19009 | hp2 | a0003 | c0003 | t0006 | g0055 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19012 | hp2 | a0002 | c0002 | t0008 | g0003 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | LWK | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | LWK | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | LWK | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | LWK | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0335 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19063 | hp1 | a0001 | c0001 | t0008 | g0075 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19065 | hp1 | a0002 | c0002 | t0008 | g0001 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19068 | hp2 | a0009 | c0008 | t0001 | g0233 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0363 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19078 | hp2 | a0011 | c0019 | t0003 | g0188 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0327 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0227 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0254 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19084 | hp1 | a0002 | c0002 | t0008 | g0019 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19085 | hp1 | a0001 | c0012 | t0001 | g0112 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19087 | hp1 | a0002 | c0002 | t0007 | g0004 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0325 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0263 | AFR | YRI | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA19240 | hp2 | a0003 | c0016 | t0006 | g0039 | AFR | YRI | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA20129 | hp1 | a0001 | c0001 | t0027 | g0027 | AFR | ASW | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0243 | AFR | ASW | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0278 | EUR | TSI | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | TSI | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA20805 | hp1 | a0002 | c0002 | t0007 | g0013 | EUR | TSI | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0126 | EUR | TSI | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0275 | AMR | CLM | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG01123 | hp2 | a0002 | c0002 | t0007 | g0002 | AMR | CLM | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02109 | hp2 | a0001 | c0001 | t0009 | g0346 | AFR | ACB | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0226 | AFR | ACB | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02486 | hp2 | a0001 | c0001 | t0009 | g0347 | AFR | ACB | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG02559 | hp2 | a0001 | c0001 | t0026 | g0224 | AFR | ACB | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03471 | hp1 | a0001 | c0001 | t0013 | g0220 | AFR | MSL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG03471 | hp2 | a0001 | c0001 | t0022 | g0209 | AFR | MSL | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0256 | AFR | USA | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | USA | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0036 | AFR | USA | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA20300 | hp2 | a0002 | c0002 | t0007 | g0010 | AFR | USA | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | LWK | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | LWK | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0149 | REF | REF | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0125 | REF | REF | RAB3GAP2_chr1_220143293_220277453 | RAB3GAP2 | chr1 | 220143293 | 220277453 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:220151373
|
T | C | 1 | a0006 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.4060A>G | p.Ile1354Val | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 35/35 | 4176/7256 | 4060/4182 | 1354/1393 | chr1 | 220151373 | ||
| chr1:220153271
|
G | A | 1 | a0007 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.3781C>T | p.His1261Tyr | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 33/35 | 3897/7256 | 3781/4182 | 1261/1393 | chr1 | 220153271 | ||
| chr1:220157863
|
C | G | 1 | a0002 | 25 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(22): Show |
missense_variant | MODERATE | c.3275G>C | p.Ser1092Thr | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 30/35 | 3391/7256 | 3275/4182 | 1092/1393 | chr1 | 220157863 | ||
| chr1:220164744
|
T | C | 1 | a0008 | 1 | NA18942.hp2 | missense_variant | MODERATE | c.3143A>G | p.His1048Arg | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/35 | 3259/7256 | 3143/4182 | 1048/1393 | chr1 | 220164744 | ||
| chr1:220170955
|
A | G | 1 | a0005 | 1 | NA18961.hp2 | missense_variant | MODERATE | c.2743T>C | p.Ser915Pro | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 24/35 | 2859/7256 | 2743/4182 | 915/1393 | chr1 | 220170955 | ||
| chr1:220171111
|
T | C | 1 | a0003 | 19 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(16): Show |
missense_variant | MODERATE | c.2587A>G | p.Thr863Ala | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 24/35 | 2703/7256 | 2587/4182 | 863/1393 | chr1 | 220171111 | ||
| chr1:220182814
|
C | G | 1 | a0009 | 1 | NA19068.hp2 | missense_variant | MODERATE | c.2116G>C | p.Gly706Arg | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 20/35 | 2232/7256 | 2116/4182 | 706/1393 | chr1 | 220182814 | ||
| chr1:220182922
|
G | C | 1 | a0004 | 2 | HG03669.hp1 HG04115.hp1 |
missense_variant | MODERATE | c.2008C>G | p.Leu670Val | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 20/35 | 2124/7256 | 2008/4182 | 670/1393 | chr1 | 220182922 | ||
| chr1:220210480
|
G | C | 1 | a0010 | 1 | NA18953.hp2 | missense_variant | MODERATE | c.520C>G | p.Leu174Val | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/35 | 636/7256 | 520/4182 | 174/1393 | chr1 | 220210480 | ||
| chr1:220213893
|
CATAAGAT others(9): Show |
C | 1 | a0011 | 1 | NA19078.hp2 | frameshift_variant | HIGH | c.251_266delCAACCAAT others(8): Show |
p.Pro84fs | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 3/35 | 382/7256 | 251/4182 | 84/1393 | chr1 | 220213893 | ||
| chr1:220272252
|
A | C | 1 | a0012 | 1 | NA19005.hp1 | missense_variant | MODERATE | c.86T>G | p.Ile29Ser | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/35 | 202/7256 | 86/4182 | 29/1393 | chr1 | 220272252 | ||
| chr1:220272289
|
C | A | 1 | a0013 | 1 | NA18986.hp1 | missense_variant | MODERATE | c.49G>T | p.Ala17Ser | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/35 | 165/7256 | 49/4182 | 17/1393 | chr1 | 220272289 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:220151666
|
T | C | 1 | a0001c0011 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.3966A>G | p.Lys1322Lys | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 34/35 | 4082/7256 | 3966/4182 | 1322/1393 | chr1 | 220151666 | ||
| chr1:220151708
|
C | G | 1 | a0003c0016 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.3924G>C | p.Thr1308Thr | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 34/35 | 4040/7256 | 3924/4182 | 1308/1393 | chr1 | 220151708 | ||
| chr1:220151741
|
T | C | 1 | a0001c0012 | 1 | NA19085.hp1 | synonymous_variant | LOW | c.3891A>G | p.Lys1297Lys | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 34/35 | 4007/7256 | 3891/4182 | 1297/1393 | chr1 | 220151741 | ||
| chr1:220153350
|
G | A | 1 | a0001c0014 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.3702C>T | p.Val1234Val | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 33/35 | 3818/7256 | 3702/4182 | 1234/1393 | chr1 | 220153350 | ||
| chr1:220157330
|
C | T | 2 | a0002c0002a0002c0007 | 25 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(22): Show |
synonymous_variant | LOW | c.3495G>A | p.Leu1165Leu | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 31/35 | 3611/7256 | 3495/4182 | 1165/1393 | chr1 | 220157330 | ||
| chr1:220182272
|
G | A | 1 | a0001c0017 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.2295C>T | p.Ser765Ser | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/35 | 2411/7256 | 2295/4182 | 765/1393 | chr1 | 220182272 | ||
| chr1:220182842
|
T | C | 2 | a0001c0004a0001c0020 | 9 | HG01433.hp1 HG02055.hp1 HG02572.hp2 others(6): Show |
synonymous_variant | LOW | c.2088A>G | p.Thr696Thr | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 20/35 | 2204/7256 | 2088/4182 | 696/1393 | chr1 | 220182842 | ||
| chr1:220232799
|
A | T | 1 | a0002c0007 | 1 | HG00558.hp1 | splice_region_variant&synonymous_variant | LOW | c.180T>A | p.Pro60Pro | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/35 | 296/7256 | 180/4182 | 60/1393 | chr1 | 220232799 | ||
| chr1:220272266
|
G | A | 1 | a0001c0020 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.72C>T | p.His24His | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/35 | 188/7256 | 72/4182 | 24/1393 | chr1 | 220272266 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:220148325
|
TAAG | T | 10 | a0001c0001t0003a0001c0001t0012a0001c0001t0016others(7): Show | 55 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*2923_*2925delCTT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 35/35 | 2923 | chr1 | 220148325 | |||||
| chr1:220148613
|
G | A | 2 | a0001c0001t0013a0001c0001t0024 | 4 | HG02055.hp2 HG02723.hp2 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2638C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 35/35 | 2638 | chr1 | 220148613 | |||||
| chr1:220148738
|
C | CT | 5 | a0001c0001t0009a0001c0001t0015a0001c0001t0030others(2): Show | 15 | HG01261.hp2 HG01884.hp2 HG02055.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2512dupA | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 35/35 | 2512 | chr1 | 220148738 | |||||
| chr1:220148852
|
T | C | 1 | a0001c0001t0017 | 2 | HG01891.hp1 HG02572.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2399A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 35/35 | 2399 | chr1 | 220148852 | |||||
| chr1:220148985
|
CACTACTG others(6): Show |
C | 1 | a0001c0001t0025 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2253_*2265delAGTA others(9): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 35/35 | 2253 | chr1 | 220148985 | |||||
| chr1:220149380
|
T | G | 2 | a0001c0001t0022a0001c0001t0026 | 2 | HG02559.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1871A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 35/35 | 1871 | chr1 | 220149380 | |||||
| chr1:220149460
|
A | G | 1 | a0001c0001t0031 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1791T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 35/35 | 1791 | chr1 | 220149460 | |||||
| chr1:220149556
|
A | ATGT | 3 | a0001c0001t0005a0001c0001t0023a0008c0015t0005 | 18 | HG00609.hp1 HG01081.hp1 HG01346.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1694_*1695insACA | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 35/35 | 1694 | chr1 | 220149556 | |||||
| chr1:220149615
|
G | C | 1 | a0001c0001t0027 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1636C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 35/35 | 1636 | chr1 | 220149615 | |||||
| chr1:220149724
|
C | G | 1 | a0001c0001t0015 | 2 | HG01261.hp2 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1527G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 35/35 | 1527 | chr1 | 220149724 | |||||
| chr1:220149747
|
C | A | 4 | a0001c0001t0004a0001c0001t0031a0001c0001t0032others(1): Show | 48 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1504G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 35/35 | 1504 | chr1 | 220149747 | |||||
| chr1:220149847
|
A | G | 2 | a0001c0001t0015a0001c0001t0030 | 3 | HG01261.hp2 HG02630.hp1 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1404T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 35/35 | 1404 | chr1 | 220149847 | |||||
| chr1:220150106
|
CT | C | 37 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(34): Show | 249 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*1144delA | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 35/35 | 1144 | chr1 | 220150106 | |||||
| chr1:220150108
|
T | C | 1 | a0001c0001t0028 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1143A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 35/35 | 1143 | chr1 | 220150108 | |||||
| chr1:220150121
|
T | C | 1 | a0001c0001t0029 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1130A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 35/35 | 1130 | chr1 | 220150121 | |||||
| chr1:220150326
|
G | A | 2 | a0001c0001t0010a0001c0001t0021 | 5 | HG01258.hp1 HG01934.hp1 HG02004.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*925C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 35/35 | 925 | chr1 | 220150326 | |||||
| chr1:220150451
|
C | CT | 7 | a0001c0001t0007a0001c0001t0011a0001c0001t0014others(4): Show | 23 | HG00423.hp1 HG01074.hp2 HG01123.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*799dupA | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 35/35 | 799 | chr1 | 220150451 | |||||
| chr1:220150451
|
CT | C | 14 | a0001c0001t0004a0001c0001t0006a0001c0001t0009others(11): Show | 84 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*799delA | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 35/35 | 799 | chr1 | 220150451 | |||||
| chr1:220150488
|
A | G | 1 | a0001c0001t0034 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*763T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 35/35 | 763 | chr1 | 220150488 | |||||
| chr1:220150847
|
A | G | 5 | a0001c0001t0007a0001c0001t0008a0002c0002t0007others(2): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*404T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 35/35 | 404 | chr1 | 220150847 | |||||
| chr1:220150860
|
G | A | 1 | a0001c0001t0033 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*391C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 35/35 | 391 | chr1 | 220150860 | |||||
| chr1:220150900
|
G | T | 1 | a0001c0001t0018 | 1 | NA18944.hp2 | 3_prime_UTR_variant | MODIFIER | c.*351C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 35/35 | 351 | chr1 | 220150900 | |||||
| chr1:220272385
|
T | C | 1 | a0001c0001t0034 | 1 | HG03041.hp2 | 5_prime_UTR_variant | MODIFIER | c.-48A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/35 | 48 | chr1 | 220272385 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:220151547
|
C | G | 14 | a0001c0001t0002g0061a0001c0001t0009g0343a0001c0001t0009g0344others(11): Show | 15 | HG01433.hp1 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.4026+59G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 34/34 | chr1 | 220151547 | ||||||
| chr1:220151795
|
G | C | 20 | a0001c0001t0005g0152a0003c0003t0002g0037a0003c0003t0002g0043others(17): Show | 20 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.3868-31C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 33/34 | chr1 | 220151795 | ||||||
| chr1:220152101
|
A | C | 2 | a0001c0001t0017g0216a0001c0001t0017g0217 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.3868-337T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 33/34 | chr1 | 220152101 | ||||||
| chr1:220152232
|
C | T | 1 | a0001c0001t0034g0370 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3868-468G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 33/34 | chr1 | 220152232 | ||||||
| chr1:220152336
|
C | A | 3 | a0001c0001t0002g0235a0001c0001t0002g0350a0001c0001t0026g0224 | 3 | HG02258.hp2 HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3868-572G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 33/34 | chr1 | 220152336 | ||||||
| chr1:220152349
|
T | A | 2 | a0001c0001t0017g0216a0001c0001t0017g0217 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.3868-585A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 33/34 | chr1 | 220152349 | ||||||
| chr1:220152631
|
C | T | 1 | a0002c0002t0008g0001 | 3 | NA18942.hp1 NA18994.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.3867+554G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 33/34 | chr1 | 220152631 | ||||||
| chr1:220152632
|
G | A | 2 | a0001c0001t0003g0200a0001c0001t0003g0201 | 2 | NA18998.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.3867+553C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 33/34 | chr1 | 220152632 | ||||||
| chr1:220152746
|
G | A | 1 | a0001c0001t0020g0170 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3867+439C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 33/34 | chr1 | 220152746 | ||||||
| chr1:220152798
|
C | G | 15 | a0001c0001t0009g0343a0001c0001t0009g0344a0001c0001t0009g0346others(12): Show | 16 | HG01261.hp2 HG01433.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.3867+387G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 33/34 | chr1 | 220152798 | ||||||
| chr1:220152833
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3867+352G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 33/34 | chr1 | 220152833 | ||||||
| chr1:220153152
|
G | C | 1 | a0001c0001t0001g0244 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3867+33C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 33/34 | chr1 | 220153152 | ||||||
| chr1:220153591
|
T | A | 4 | a0001c0001t0002g0350a0002c0002t0007g0004a0002c0002t0007g0022others(1): Show | 5 | HG00423.hp1 HG02258.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.3646-185A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 32/34 | chr1 | 220153591 | ||||||
| chr1:220153723
|
G | A | 1 | a0001c0001t0003g0196 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.3645+245C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 32/34 | chr1 | 220153723 | ||||||
| chr1:220154084
|
G | A | 1 | a0001c0001t0004g0326 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3556-27C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 31/34 | chr1 | 220154084 | ||||||
| chr1:220154102
|
AG | A | 51 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0247others(48): Show | 51 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.3556-46delC | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 31/34 | chr1 | 220154102 | ||||||
| chr1:220154232
|
A | G | 2 | a0001c0001t0017g0216a0001c0001t0017g0217 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.3556-175T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 31/34 | chr1 | 220154232 | ||||||
| chr1:220154267
|
G | A | 1 | a0001c0001t0003g0202 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3556-210C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 31/34 | chr1 | 220154267 | ||||||
| chr1:220154437
|
G | A | 3 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0006g0108 | 3 | HG02559.hp1 HG02735.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.3556-380C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 31/34 | chr1 | 220154437 | ||||||
| chr1:220154443
|
T | C | 2 | a0001c0001t0002g0307a0001c0001t0002g0309 | 2 | NA18955.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.3556-386A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 31/34 | chr1 | 220154443 | ||||||
| chr1:220154721
|
C | CT | 139 | a0001c0001t0001g0072a0001c0001t0001g0083a0001c0001t0001g0085others(136): Show | 145 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.3556-665dupA | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 31/34 | chr1 | 220154721 | ||||||
| chr1:220154721
|
C | CTT | 38 | a0001c0001t0001g0261a0001c0001t0002g0181a0001c0001t0003g0005others(35): Show | 39 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.3556-666_3556-665d others(4): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 31/34 | chr1 | 220154721 | ||||||
| chr1:220154877
|
C | T | 1 | a0003c0003t0006g0046 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3556-820G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 31/34 | chr1 | 220154877 | ||||||
| chr1:220154883
|
G | C | 1 | a0001c0001t0002g0288 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.3556-826C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 31/34 | chr1 | 220154883 | ||||||
| chr1:220155020
|
C | T | 6 | a0001c0001t0003g0241a0001c0001t0004g0240a0001c0001t0004g0251others(3): Show | 6 | HG02015.hp1 HG02135.hp2 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.3556-963G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 31/34 | chr1 | 220155020 | ||||||
| chr1:220155069
|
T | C | 1 | a0002c0002t0007g0011 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3556-1012A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 31/34 | chr1 | 220155069 | ||||||
| chr1:220155157
|
A | G | 1 | a0001c0001t0023g0141 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.3556-1100T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 31/34 | chr1 | 220155157 | ||||||
| chr1:220155224
|
C | A | 1 | a0001c0001t0001g0101 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3556-1167G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 31/34 | chr1 | 220155224 | ||||||
| chr1:220155285
|
G | T | 1 | a0001c0001t0013g0221 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3556-1228C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 31/34 | chr1 | 220155285 | ||||||
| chr1:220155464
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.3556-1407A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 31/34 | chr1 | 220155464 | ||||||
| chr1:220155473
|
A | G | 3 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024 | 3 | HG02027.hp2 NA18975.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.3556-1416T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 31/34 | chr1 | 220155473 | ||||||
| chr1:220155831
|
G | C | 22 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0074others(19): Show | 22 | HG01358.hp2 HG01496.hp1 HG01934.hp2 others(19): Show |
intron_variant | MODIFIER | c.3555+1439C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 31/34 | chr1 | 220155831 | ||||||
| chr1:220155931
|
T | C | 1 | a0003c0003t0006g0041 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3555+1339A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 31/34 | chr1 | 220155931 | ||||||
| chr1:220156140
|
A | G | 1 | a0003c0003t0006g0046 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3555+1130T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 31/34 | chr1 | 220156140 | ||||||
| chr1:220156153
|
G | T | 2 | a0001c0001t0017g0216a0001c0001t0017g0217 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.3555+1117C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 31/34 | chr1 | 220156153 | ||||||
| chr1:220156242
|
T | C | 22 | a0001c0001t0005g0152a0001c0001t0017g0216a0001c0001t0017g0217others(19): Show | 22 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.3555+1028A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 31/34 | chr1 | 220156242 | ||||||
| chr1:220156815
|
T | C | 2 | a0001c0001t0017g0216a0001c0001t0017g0217 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.3555+455A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 31/34 | chr1 | 220156815 | ||||||
| chr1:220156844
|
G | A | 20 | a0001c0001t0005g0152a0003c0003t0002g0037a0003c0003t0002g0043others(17): Show | 20 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.3555+426C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 31/34 | chr1 | 220156844 | ||||||
| chr1:220157014
|
G | A | 6 | a0001c0001t0003g0241a0001c0001t0004g0240a0001c0001t0004g0251others(3): Show | 6 | HG02015.hp1 HG02135.hp2 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.3555+256C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 31/34 | chr1 | 220157014 | ||||||
| chr1:220157664
|
C | T | 4 | a0001c0001t0003g0179a0001c0001t0003g0184a0001c0001t0003g0194others(1): Show | 4 | NA18939.hp2 NA19002.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.3336+138G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 30/34 | chr1 | 220157664 | ||||||
| chr1:220157694
|
A | C | 1 | a0001c0001t0001g0092 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3336+108T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 30/34 | chr1 | 220157694 | ||||||
| chr1:220157956
|
C | G | 20 | a0002c0002t0007g0002a0002c0002t0007g0004a0002c0002t0007g0009others(17): Show | 25 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.3262-80G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 29/34 | chr1 | 220157956 | ||||||
| chr1:220157977
|
T | G | 56 | a0001c0001t0002g0071a0001c0001t0002g0133a0001c0001t0002g0206others(53): Show | 56 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.3262-101A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 29/34 | chr1 | 220157977 | ||||||
| chr1:220158301
|
T | C | 1 | a0001c0001t0016g0173 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3262-425A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 29/34 | chr1 | 220158301 | ||||||
| chr1:220158315
|
G | A | 12 | a0001c0001t0009g0343a0001c0001t0009g0344a0001c0001t0009g0346others(9): Show | 13 | HG01433.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.3262-439C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 29/34 | chr1 | 220158315 | ||||||
| chr1:220158504
|
G | A | 6 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0131others(3): Show | 6 | HG01071.hp1 HG01074.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.3262-628C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 29/34 | chr1 | 220158504 | ||||||
| chr1:220158526
|
C | T | 1 | a0001c0020t0009g0368 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3262-650G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 29/34 | chr1 | 220158526 | ||||||
| chr1:220158619
|
T | C | 124 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0032others(121): Show | 126 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.3262-743A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 29/34 | chr1 | 220158619 | ||||||
| chr1:220158733
|
G | A | 1 | a0001c0001t0009g0344 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3261+653C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 29/34 | chr1 | 220158733 | ||||||
| chr1:220158766
|
CT | C | 224 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0244others(221): Show | 227 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(224): Show |
intron_variant | MODIFIER | c.3261+619delA | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 29/34 | chr1 | 220158766 | ||||||
| chr1:220158785
|
C | T | 1 | a0003c0003t0006g0041 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3261+601G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 29/34 | chr1 | 220158785 | ||||||
| chr1:220158925
|
C | A | 1 | a0001c0001t0017g0217 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3261+461G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 29/34 | chr1 | 220158925 | ||||||
| chr1:220159210
|
C | T | 244 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0244others(241): Show | 252 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(249): Show |
intron_variant | MODIFIER | c.3261+176G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 29/34 | chr1 | 220159210 | ||||||
| chr1:220159280
|
C | T | 1 | a0001c0001t0027g0027 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3261+106G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 29/34 | chr1 | 220159280 | ||||||
| chr1:220159348
|
T | G | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3261+38A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 29/34 | chr1 | 220159348 | ||||||
| chr1:220159493
|
T | TA | 70 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0247others(67): Show | 71 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.3226-73dupT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 28/34 | chr1 | 220159493 | ||||||
| chr1:220159534
|
G | A | 244 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0244others(241): Show | 252 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(249): Show |
intron_variant | MODIFIER | c.3226-113C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 28/34 | chr1 | 220159534 | ||||||
| chr1:220159826
|
C | T | 19 | a0003c0003t0002g0037a0003c0003t0002g0043a0003c0003t0002g0053others(16): Show | 19 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.3226-405G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 28/34 | chr1 | 220159826 | ||||||
| chr1:220159932
|
A | C | 16 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(13): Show | 16 | NA18747.hp1 NA18939.hp1 NA18943.hp2 others(13): Show |
intron_variant | MODIFIER | c.3226-511T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 28/34 | chr1 | 220159932 | ||||||
| chr1:220159957
|
C | T | 1 | a0001c0001t0001g0261 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3226-536G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 28/34 | chr1 | 220159957 | ||||||
| chr1:220159959
|
G | A | 20 | a0002c0002t0007g0002a0002c0002t0007g0004a0002c0002t0007g0009others(17): Show | 25 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.3226-538C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 28/34 | chr1 | 220159959 | ||||||
| chr1:220159983
|
C | T | 1 | a0001c0001t0002g0298 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.3226-562G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 28/34 | chr1 | 220159983 | ||||||
| chr1:220160475
|
C | A | 20 | a0002c0002t0007g0002a0002c0002t0007g0004a0002c0002t0007g0009others(17): Show | 25 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.3226-1054G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 28/34 | chr1 | 220160475 | ||||||
| chr1:220160615
|
T | C | 20 | a0001c0001t0005g0152a0003c0003t0002g0037a0003c0003t0002g0043others(17): Show | 20 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.3226-1194A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 28/34 | chr1 | 220160615 | ||||||
| chr1:220160661
|
T | C | 1 | a0001c0001t0004g0259 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3226-1240A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 28/34 | chr1 | 220160661 | ||||||
| chr1:220160710
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3226-1289A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 28/34 | chr1 | 220160710 | ||||||
| chr1:220160821
|
T | C | 67 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0247others(64): Show | 68 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.3225+1377A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 28/34 | chr1 | 220160821 | ||||||
| chr1:220161018
|
T | C | 2 | a0003c0003t0002g0037a0003c0003t0002g0043 | 2 | HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.3225+1180A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 28/34 | chr1 | 220161018 | ||||||
| chr1:220161089
|
G | A | 2 | a0001c0001t0017g0216a0001c0001t0017g0217 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.3225+1109C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 28/34 | chr1 | 220161089 | ||||||
| chr1:220161096
|
G | A | 15 | a0001c0001t0001g0065a0001c0001t0003g0094a0001c0001t0004g0093others(12): Show | 15 | HG00609.hp1 HG03491.hp2 HG03688.hp1 others(12): Show |
intron_variant | MODIFIER | c.3225+1102C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 28/34 | chr1 | 220161096 | ||||||
| chr1:220161308
|
A | T | 20 | a0002c0002t0007g0002a0002c0002t0007g0004a0002c0002t0007g0009others(17): Show | 25 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.3225+890T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 28/34 | chr1 | 220161308 | ||||||
| chr1:220161590
|
T | C | 1 | a0001c0001t0004g0232 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.3225+608A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 28/34 | chr1 | 220161590 | ||||||
| chr1:220162088
|
A | G | 139 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(136): Show | 141 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.3225+110T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 28/34 | chr1 | 220162088 | ||||||
| chr1:220162146
|
G | A | 3 | a0001c0001t0003g0192a0001c0001t0003g0335a0001c0001t0008g0075 | 3 | NA19004.hp1 NA19058.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.3225+52C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 28/34 | chr1 | 220162146 | ||||||
| chr1:220162365
|
C | A | 1 | a0001c0001t0004g0236 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3155-97G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220162365 | ||||||
| chr1:220162383
|
T | C | 7 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0032others(4): Show | 7 | HG02145.hp2 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.3155-115A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220162383 | ||||||
| chr1:220162404
|
T | C | 4 | a0001c0001t0002g0235a0001c0001t0002g0350a0001c0001t0022g0209others(1): Show | 4 | HG02258.hp2 HG02559.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3155-136A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220162404 | ||||||
| chr1:220162409
|
T | C | 4 | a0001c0001t0002g0235a0001c0001t0002g0350a0001c0001t0022g0209others(1): Show | 4 | HG02258.hp2 HG02559.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3155-141A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220162409 | ||||||
| chr1:220162462
|
G | C | 14 | a0001c0001t0005g0152a0003c0003t0002g0053a0003c0003t0002g0054others(11): Show | 14 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.3155-194C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220162462 | ||||||
| chr1:220162666
|
T | C | 1 | a0001c0001t0001g0086 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3155-398A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220162666 | ||||||
| chr1:220163335
|
A | C | 20 | a0001c0001t0005g0152a0003c0003t0002g0037a0003c0003t0002g0043others(17): Show | 20 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.3155-1067T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163335 | ||||||
| chr1:220163657
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3154+1076G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163657 | ||||||
| chr1:220163736
|
A | AATAC | 3 | a0001c0001t0001g0085a0001c0001t0001g0244a0001c0001t0003g0196 | 3 | HG02895.hp1 NA18979.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.3154+993_3154+996d others(6): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163736 | ||||||
| chr1:220163740
|
C | CAT | 20 | a0001c0001t0001g0026a0001c0001t0001g0047a0001c0001t0001g0100others(17): Show | 20 | HG00140.hp1 HG00609.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.3154+991_3154+992d others(4): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163740 | ||||||
| chr1:220163740
|
C | CATAT | 9 | a0001c0001t0001g0062a0001c0001t0001g0101a0001c0001t0001g0107others(6): Show | 9 | HG01256.hp1 HG01981.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.3154+992_3154+993i others(6): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163740 | ||||||
| chr1:220163740
|
C | CATATATA others(5): Show |
1 | a0001c0001t0001g0116 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.3154+992_3154+993i others(14): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163740 | ||||||
| chr1:220163740
|
CATACATA others(3): Show |
C | 1 | a0001c0001t0001g0145 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3154+983_3154+992d others(12): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163740 | ||||||
| chr1:220163742
|
TAC | T | 3 | a0001c0001t0001g0065a0001c0001t0001g0166a0001c0001t0001g0355 | 3 | HG02148.hp1 HG03688.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.3154+989_3154+990d others(4): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163742 | ||||||
| chr1:220163744
|
C | CAT | 25 | a0001c0001t0001g0069a0001c0001t0001g0077a0001c0001t0001g0078others(22): Show | 28 | HG00597.hp2 HG00621.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.3154+987_3154+988d others(4): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163744 | ||||||
| chr1:220163744
|
C | CATACAT | 8 | a0001c0001t0001g0261a0001c0001t0002g0297a0001c0001t0002g0315others(5): Show | 8 | HG00741.hp1 HG01358.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.3154+988_3154+989i others(8): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163744 | ||||||
| chr1:220163744
|
C | CATACATA others(7): Show |
1 | a0001c0001t0034g0370 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3154+988_3154+989i others(16): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163744 | ||||||
| chr1:220163744
|
C | CATACATA others(1): Show |
65 | a0001c0001t0001g0341a0001c0001t0002g0133a0001c0001t0002g0211others(62): Show | 66 | HG00140.hp2 HG00558.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.3154+988_3154+989i others(10): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163744 | ||||||
| chr1:220163744
|
C | CATACATA others(3): Show |
28 | a0001c0001t0002g0061a0001c0001t0002g0071a0001c0001t0002g0181others(25): Show | 29 | HG01123.hp1 HG01243.hp1 HG01516.hp1 others(26): Show |
intron_variant | MODIFIER | c.3154+988_3154+989i others(12): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163744 | ||||||
| chr1:220163744
|
C | CATACATA others(5): Show |
11 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0044others(8): Show | 11 | HG00408.hp2 HG00544.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.3154+988_3154+989i others(14): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163744 | ||||||
| chr1:220163744
|
C | CATACATA others(7): Show |
6 | a0001c0001t0001g0092a0001c0001t0002g0033a0001c0001t0002g0205others(3): Show | 6 | HG02109.hp1 HG02145.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.3154+988_3154+989i others(16): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163744 | ||||||
| chr1:220163744
|
C | CATACATA others(9): Show |
5 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0120others(2): Show | 5 | HG02040.hp2 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.3154+988_3154+989i others(18): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163744 | ||||||
| chr1:220163744
|
C | CATACATA others(11): Show |
2 | a0001c0001t0002g0032a0001c0001t0003g0189 | 2 | HG00673.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.3154+988_3154+989i others(20): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163744 | ||||||
| chr1:220163744
|
C | CATACATA others(13): Show |
1 | a0001c0001t0002g0040 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3154+988_3154+989i others(22): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163744 | ||||||
| chr1:220163744
|
C | CATAT | 42 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0083others(39): Show | 43 | HG00544.hp2 HG01243.hp2 HG01346.hp2 others(40): Show |
intron_variant | MODIFIER | c.3154+985_3154+988d others(6): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163744 | ||||||
| chr1:220163744
|
C | CATATAT | 19 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(16): Show | 19 | HG00423.hp1 HG00423.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.3154+983_3154+988d others(8): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163744 | ||||||
| chr1:220163744
|
C | CATATATA others(1): Show |
3 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0004g0256 | 3 | HG06807.hp1 NA18955.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.3154+981_3154+988d others(10): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163744 | ||||||
| chr1:220163744
|
C | CATATATA others(3): Show |
2 | a0001c0001t0004g0253a0001c0001t0017g0216 | 2 | HG01891.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.3154+979_3154+988d others(12): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163744 | ||||||
| chr1:220163744
|
C | CATATATA others(5): Show |
1 | a0001c0001t0003g0241 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3154+977_3154+988d others(14): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163744 | ||||||
| chr1:220163744
|
C | T | 83 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(80): Show | 83 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.3154+989G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163744 | ||||||
| chr1:220163744
|
CAT | C | 6 | a0001c0001t0004g0237a0001c0001t0004g0238a0001c0001t0004g0239others(3): Show | 6 | HG02615.hp1 HG02723.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.3154+987_3154+988d others(4): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163744 | ||||||
| chr1:220163744
|
CATAT | C | 9 | a0002c0002t0007g0002a0002c0002t0007g0010a0002c0002t0007g0011others(6): Show | 10 | HG00639.hp1 HG01123.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.3154+985_3154+988d others(6): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163744 | ||||||
| chr1:220163744
|
CATATAT | C | 4 | a0001c0001t0002g0214a0001c0001t0030g0348a0001c0014t0001g0269others(1): Show | 4 | HG01074.hp2 HG02809.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3154+983_3154+988d others(8): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163744 | ||||||
| chr1:220163744
|
CATATATA others(3): Show |
C | 12 | a0001c0001t0009g0343a0001c0001t0009g0344a0001c0001t0009g0346others(9): Show | 13 | HG01433.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.3154+979_3154+988d others(12): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163744 | ||||||
| chr1:220163754
|
T | C | 1 | a0001c0001t0002g0214 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3154+979A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163754 | ||||||
| chr1:220163756
|
T | C | 1 | a0001c0001t0003g0266 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3154+977A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163756 | ||||||
| chr1:220163758
|
T | A | 1 | a0002c0002t0008g0021 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3154+975A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163758 | ||||||
| chr1:220163886
|
T | C | 2 | a0001c0001t0001g0059a0001c0001t0002g0060 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3154+847A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220163886 | ||||||
| chr1:220164473
|
G | GT | 22 | a0001c0001t0001g0064a0001c0001t0001g0132a0001c0001t0001g0157others(19): Show | 23 | HG01433.hp1 HG01884.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.3154+259dupA | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220164473 | ||||||
| chr1:220164473
|
G | T | 1 | a0001c0001t0001g0072 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3154+260C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220164473 | ||||||
| chr1:220164473
|
GT | G | 153 | a0001c0001t0001g0247a0001c0001t0002g0030a0001c0001t0002g0031others(150): Show | 160 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.3154+259delA | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220164473 | ||||||
| chr1:220164548
|
C | T | 1 | a0001c0001t0002g0061 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3154+185G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 27/34 | chr1 | 220164548 | ||||||
| chr1:220165199
|
T | C | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3088-400A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 26/34 | chr1 | 220165199 | ||||||
| chr1:220165332
|
G | A | 1 | a0001c0001t0006g0364 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3088-533C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 26/34 | chr1 | 220165332 | ||||||
| chr1:220165547
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3088-748A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 26/34 | chr1 | 220165547 | ||||||
| chr1:220165649
|
AAAAC | A | 4 | a0001c0001t0013g0219a0001c0001t0013g0220a0001c0001t0013g0221others(1): Show | 4 | HG02055.hp2 HG02723.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.3088-854_3088-851d others(6): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 26/34 | chr1 | 220165649 | ||||||
| chr1:220165829
|
C | T | 1 | a0001c0001t0002g0214 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3088-1030G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 26/34 | chr1 | 220165829 | ||||||
| chr1:220166137
|
G | A | 70 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0247others(67): Show | 71 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.3087+1156C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 26/34 | chr1 | 220166137 | ||||||
| chr1:220166550
|
G | A | 1 | a0001c0001t0002g0312 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.3087+743C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 26/34 | chr1 | 220166550 | ||||||
| chr1:220166714
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3087+579G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 26/34 | chr1 | 220166714 | ||||||
| chr1:220166753
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3087+540C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 26/34 | chr1 | 220166753 | ||||||
| chr1:220166780
|
TACAGAAG others(2): Show |
T | 20 | a0002c0002t0007g0002a0002c0002t0007g0004a0002c0002t0007g0009others(17): Show | 25 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.3087+504_3087+512d others(11): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 26/34 | chr1 | 220166780 | ||||||
| chr1:220166860
|
C | T | 19 | a0003c0003t0002g0037a0003c0003t0002g0043a0003c0003t0002g0053others(16): Show | 19 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.3087+433G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 26/34 | chr1 | 220166860 | ||||||
| chr1:220167072
|
T | C | 1 | a0001c0001t0001g0025 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3087+221A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 26/34 | chr1 | 220167072 | ||||||
| chr1:220167250
|
C | A | 1 | a0001c0001t0002g0306 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3087+43G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 26/34 | chr1 | 220167250 | ||||||
| chr1:220167765
|
T | A | 1 | a0001c0017t0001g0234 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2807-90A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 24/34 | chr1 | 220167765 | ||||||
| chr1:220168051
|
A | T | 19 | a0003c0003t0002g0037a0003c0003t0002g0043a0003c0003t0002g0053others(16): Show | 19 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.2807-376T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 24/34 | chr1 | 220168051 | ||||||
| chr1:220168162
|
A | C | 20 | a0002c0002t0007g0002a0002c0002t0007g0004a0002c0002t0007g0009others(17): Show | 25 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.2807-487T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 24/34 | chr1 | 220168162 | ||||||
| chr1:220168210
|
A | G | 1 | a0001c0001t0001g0166 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2807-535T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 24/34 | chr1 | 220168210 | ||||||
| chr1:220168238
|
G | A | 1 | a0001c0001t0003g0243 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2807-563C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 24/34 | chr1 | 220168238 | ||||||
| chr1:220168315
|
C | T | 1 | a0002c0002t0007g0011 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2807-640G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 24/34 | chr1 | 220168315 | ||||||
| chr1:220168350
|
C | G | 7 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0032others(4): Show | 7 | HG02145.hp2 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2807-675G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 24/34 | chr1 | 220168350 | ||||||
| chr1:220168399
|
C | CT | 11 | a0001c0001t0002g0281a0001c0001t0002g0282a0001c0001t0002g0283others(8): Show | 11 | HG01891.hp1 HG02615.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.2807-725dupA | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 24/34 | chr1 | 220168399 | ||||||
| chr1:220168430
|
T | C | 1 | a0001c0001t0005g0152 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2807-755A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 24/34 | chr1 | 220168430 | ||||||
| chr1:220168639
|
C | T | 3 | a0001c0001t0001g0244a0001c0001t0001g0261a0001c0001t0001g0341 | 3 | HG02615.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2807-964G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 24/34 | chr1 | 220168639 | ||||||
| chr1:220168746
|
C | A | 1 | a0001c0001t0034g0370 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2807-1071G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 24/34 | chr1 | 220168746 | ||||||
| chr1:220168822
|
G | A | 1 | a0001c0001t0002g0302 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2807-1147C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 24/34 | chr1 | 220168822 | ||||||
| chr1:220168877
|
T | C | 4 | a0001c0001t0002g0235a0001c0001t0002g0350a0001c0001t0022g0209others(1): Show | 4 | HG02258.hp2 HG02559.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2807-1202A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 24/34 | chr1 | 220168877 | ||||||
| chr1:220168879
|
C | T | 3 | a0002c0002t0007g0004a0002c0002t0007g0022a0002c0002t0007g0023 | 4 | HG00423.hp1 NA18954.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.2807-1204G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 24/34 | chr1 | 220168879 | ||||||
| chr1:220168891
|
C | T | 1 | a0011c0019t0003g0188 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2807-1216G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 24/34 | chr1 | 220168891 | ||||||
| chr1:220169178
|
T | A | 2 | a0001c0001t0015g0339a0001c0001t0015g0340 | 2 | HG01261.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2807-1503A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 24/34 | chr1 | 220169178 | ||||||
| chr1:220169215
|
A | G | 18 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0066others(15): Show | 18 | HG00597.hp1 HG00621.hp2 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.2807-1540T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 24/34 | chr1 | 220169215 | ||||||
| chr1:220169385
|
G | T | 1 | a0001c0001t0002g0033 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2806+1507C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 24/34 | chr1 | 220169385 | ||||||
| chr1:220169644
|
G | T | 2 | a0001c0001t0002g0211a0001c0001t0014g0210 | 2 | HG01891.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2806+1248C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 24/34 | chr1 | 220169644 | ||||||
| chr1:220169729
|
C | T | 1 | a0003c0003t0006g0041 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2806+1163G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 24/34 | chr1 | 220169729 | ||||||
| chr1:220169809
|
C | G | 14 | a0001c0001t0005g0152a0003c0003t0002g0053a0003c0003t0002g0054others(11): Show | 14 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.2806+1083G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 24/34 | chr1 | 220169809 | ||||||
| chr1:220170445
|
C | CA | 8 | a0001c0001t0001g0341a0001c0001t0013g0219a0001c0001t0013g0220others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2806+446dupT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 24/34 | chr1 | 220170445 | ||||||
| chr1:220170474
|
T | C | 245 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0244others(242): Show | 253 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(250): Show |
intron_variant | MODIFIER | c.2806+418A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 24/34 | chr1 | 220170474 | ||||||
| chr1:220170763
|
A | G | 1 | a0001c0001t0002g0320 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2806+129T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 24/34 | chr1 | 220170763 | ||||||
| chr1:220170765
|
A | G | 1 | a0001c0001t0018g0073 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2806+127T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 24/34 | chr1 | 220170765 | ||||||
| chr1:220170806
|
T | C | 3 | a0001c0001t0002g0205a0001c0001t0003g0169a0001c0001t0003g0198 | 3 | HG02135.hp1 HG02155.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.2806+86A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 24/34 | chr1 | 220170806 | ||||||
| chr1:220170844
|
C | T | 2 | a0001c0001t0014g0246a0001c0001t0034g0370 | 2 | HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2806+48G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 24/34 | chr1 | 220170844 | ||||||
| chr1:220171184
|
C | G | 1 | a0001c0001t0002g0350 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2578-64G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 23/34 | chr1 | 220171184 | ||||||
| chr1:220171290
|
G | A | 54 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0247others(51): Show | 54 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.2578-170C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 23/34 | chr1 | 220171290 | ||||||
| chr1:220171548
|
A | C | 54 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0247others(51): Show | 54 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.2577+341T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 23/34 | chr1 | 220171548 | ||||||
| chr1:220171623
|
C | T | 3 | a0001c0004t0002g0345a0001c0004t0009g0338a0001c0004t0009g0342 | 3 | HG01433.hp1 HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2577+266G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 23/34 | chr1 | 220171623 | ||||||
| chr1:220171771
|
G | A | 1 | a0001c0001t0004g0327 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2577+118C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 23/34 | chr1 | 220171771 | ||||||
| chr1:220171793
|
C | A | 6 | a0001c0001t0001g0070a0001c0001t0001g0360a0001c0001t0001g0361others(3): Show | 6 | HG00408.hp1 NA18973.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.2577+96G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 23/34 | chr1 | 220171793 | ||||||
| chr1:220171810
|
C | T | 2 | a0001c0001t0015g0339a0001c0001t0015g0340 | 2 | HG01261.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2577+79G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 23/34 | chr1 | 220171810 | ||||||
| chr1:220172230
|
A | C | 42 | a0001c0001t0005g0152a0001c0001t0017g0216a0001c0001t0017g0217others(39): Show | 47 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.2417-181T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 22/34 | chr1 | 220172230 | ||||||
| chr1:220172352
|
A | G | 5 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(2): Show | 5 | HG02109.hp1 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2416+285T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 22/34 | chr1 | 220172352 | ||||||
| chr1:220172407
|
T | C | 1 | a0001c0001t0034g0370 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2416+230A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 22/34 | chr1 | 220172407 | ||||||
| chr1:220172518
|
C | T | 54 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0247others(51): Show | 54 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.2416+119G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 22/34 | chr1 | 220172518 | ||||||
| chr1:220172536
|
A | G | 20 | a0002c0002t0007g0002a0002c0002t0007g0004a0002c0002t0007g0009others(17): Show | 25 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.2416+101T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 22/34 | chr1 | 220172536 | ||||||
| chr1:220172537
|
C | G | 1 | a0001c0001t0010g0102 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2416+100G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 22/34 | chr1 | 220172537 | ||||||
| chr1:220172825
|
A | C | 1 | a0001c0001t0017g0216 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2311-83T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220172825 | ||||||
| chr1:220172825
|
A | G | 4 | a0001c0001t0004g0229a0001c0001t0004g0230a0001c0001t0004g0231others(1): Show | 4 | NA18612.hp2 NA18980.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.2311-83T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220172825 | ||||||
| chr1:220173097
|
T | A | 1 | a0001c0001t0005g0097 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2311-355A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220173097 | ||||||
| chr1:220173421
|
G | A | 1 | a0001c0001t0002g0287 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2311-679C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220173421 | ||||||
| chr1:220173455
|
T | C | 1 | a0001c0001t0005g0250 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2311-713A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220173455 | ||||||
| chr1:220173634
|
C | A | 20 | a0002c0002t0007g0002a0002c0002t0007g0004a0002c0002t0007g0009others(17): Show | 25 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.2311-892G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220173634 | ||||||
| chr1:220173778
|
T | G | 1 | a0001c0001t0005g0110 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2311-1036A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220173778 | ||||||
| chr1:220173803
|
G | A | 1 | a0001c0001t0014g0246 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2311-1061C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220173803 | ||||||
| chr1:220174019
|
C | CA | 13 | a0001c0001t0001g0070a0001c0001t0001g0090a0001c0001t0001g0091others(10): Show | 13 | HG00741.hp1 HG01069.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.2311-1278dupT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220174019 | ||||||
| chr1:220174034
|
A | G | 1 | a0001c0001t0003g0171 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2311-1292T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220174034 | ||||||
| chr1:220174039
|
G | A | 1 | a0001c0001t0018g0073 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2311-1297C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220174039 | ||||||
| chr1:220174223
|
G | A | 1 | a0003c0003t0006g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2311-1481C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220174223 | ||||||
| chr1:220174225
|
A | C | 2 | a0001c0001t0017g0216a0001c0001t0017g0217 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2311-1483T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220174225 | ||||||
| chr1:220174399
|
G | C | 1 | a0001c0001t0011g0081 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2311-1657C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220174399 | ||||||
| chr1:220174451
|
G | T | 1 | a0001c0001t0001g0072 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2311-1709C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220174451 | ||||||
| chr1:220174634
|
G | C | 1 | a0001c0001t0002g0276 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2311-1892C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220174634 | ||||||
| chr1:220174649
|
CT | C | 53 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0247others(50): Show | 53 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.2311-1908delA | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220174649 | ||||||
| chr1:220174816
|
C | T | 17 | a0003c0003t0002g0037a0003c0003t0002g0043a0003c0003t0002g0053others(14): Show | 17 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.2311-2074G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220174816 | ||||||
| chr1:220174897
|
C | T | 2 | a0001c0001t0011g0351a0001c0001t0011g0352 | 2 | HG01243.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2311-2155G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220174897 | ||||||
| chr1:220175366
|
G | C | 1 | a0001c0001t0002g0290 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2311-2624C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220175366 | ||||||
| chr1:220175459
|
C | T | 58 | a0001c0001t0002g0071a0001c0001t0002g0133a0001c0001t0002g0270others(55): Show | 58 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.2311-2717G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220175459 | ||||||
| chr1:220175461
|
C | A | 88 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(85): Show | 88 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.2311-2719G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220175461 | ||||||
| chr1:220175489
|
T | C | 364 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(361): Show | 372 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(369): Show |
intron_variant | MODIFIER | c.2311-2747A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220175489 | ||||||
| chr1:220175509
|
G | A | 2 | a0002c0002t0007g0004a0002c0002t0007g0022 | 3 | HG00423.hp1 NA18993.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.2311-2767C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220175509 | ||||||
| chr1:220175580
|
C | T | 1 | a0003c0003t0006g0051 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2311-2838G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220175580 | ||||||
| chr1:220175652
|
A | G | 1 | a0001c0001t0010g0103 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2311-2910T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220175652 | ||||||
| chr1:220175700
|
C | T | 1 | a0001c0001t0003g0171 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2311-2958G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220175700 | ||||||
| chr1:220176305
|
T | C | 4 | a0001c0001t0002g0280a0001c0001t0002g0288a0001c0001t0002g0289others(1): Show | 4 | NA18984.hp2 NA18988.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.2311-3563A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220176305 | ||||||
| chr1:220176311
|
A | C | 7 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0032others(4): Show | 7 | HG02145.hp2 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2311-3569T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220176311 | ||||||
| chr1:220176569
|
C | T | 1 | a0001c0001t0002g0282 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2311-3827G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220176569 | ||||||
| chr1:220176777
|
A | C | 3 | a0002c0002t0007g0004a0002c0002t0007g0022a0002c0002t0007g0023 | 4 | HG00423.hp1 NA18954.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.2311-4035T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220176777 | ||||||
| chr1:220176778
|
G | T | 3 | a0002c0002t0007g0004a0002c0002t0007g0022a0002c0002t0007g0023 | 4 | HG00423.hp1 NA18954.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.2311-4036C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220176778 | ||||||
| chr1:220176880
|
G | C | 1 | a0002c0002t0008g0014 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2311-4138C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220176880 | ||||||
| chr1:220177122
|
T | C | 1 | a0001c0001t0001g0085 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2311-4380A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220177122 | ||||||
| chr1:220177312
|
A | G | 1 | a0001c0001t0026g0224 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2311-4570T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220177312 | ||||||
| chr1:220177409
|
C | T | 338 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(335): Show | 346 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(343): Show |
intron_variant | MODIFIER | c.2311-4667G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220177409 | ||||||
| chr1:220177438
|
G | C | 3 | a0001c0001t0004g0237a0001c0001t0004g0238a0001c0001t0004g0239 | 3 | HG02723.hp1 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2311-4696C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220177438 | ||||||
| chr1:220177615
|
A | C | 1 | a0001c0001t0003g0184 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2310+4642T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220177615 | ||||||
| chr1:220177841
|
G | C | 1 | a0001c0001t0029g0117 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2310+4416C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220177841 | ||||||
| chr1:220177889
|
G | T | 1 | a0003c0003t0006g0041 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2310+4368C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220177889 | ||||||
| chr1:220178290
|
AT | A | 10 | a0002c0002t0007g0002a0002c0002t0007g0009a0002c0002t0007g0010others(7): Show | 11 | HG00639.hp1 HG01074.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.2310+3966delA | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220178290 | ||||||
| chr1:220178293
|
T | G | 1 | a0001c0001t0001g0355 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2310+3964A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220178293 | ||||||
| chr1:220178309
|
C | T | 7 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0066others(4): Show | 7 | HG00597.hp1 HG00621.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.2310+3948G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220178309 | ||||||
| chr1:220178358
|
A | G | 20 | a0002c0002t0007g0002a0002c0002t0007g0004a0002c0002t0007g0009others(17): Show | 25 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.2310+3899T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220178358 | ||||||
| chr1:220178381
|
C | T | 39 | a0001c0001t0017g0216a0001c0001t0017g0217a0002c0002t0007g0002others(36): Show | 44 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.2310+3876G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220178381 | ||||||
| chr1:220178502
|
A | T | 4 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0004g0034others(1): Show | 4 | HG02922.hp2 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2310+3755T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220178502 | ||||||
| chr1:220178512
|
C | T | 2 | a0003c0003t0002g0037a0003c0003t0002g0043 | 2 | HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.2310+3745G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220178512 | ||||||
| chr1:220178647
|
T | C | 128 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(125): Show | 130 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.2310+3610A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220178647 | ||||||
| chr1:220178709
|
T | TA | 6 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0131others(3): Show | 6 | HG01071.hp1 HG01074.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.2310+3547dupT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220178709 | ||||||
| chr1:220178878
|
C | A | 6 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0213others(3): Show | 6 | HG01891.hp2 HG02630.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.2310+3379G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220178878 | ||||||
| chr1:220178938
|
A | T | 1 | a0003c0003t0002g0037 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2310+3319T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220178938 | ||||||
| chr1:220178971
|
G | A | 3 | a0001c0001t0001g0244a0001c0001t0001g0261a0001c0001t0001g0341 | 3 | HG02615.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2310+3286C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220178971 | ||||||
| chr1:220179244
|
C | CA | 141 | a0001c0001t0001g0064a0001c0001t0001g0078a0001c0001t0001g0090others(138): Show | 144 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.2310+3012dupT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220179244 | ||||||
| chr1:220179244
|
C | CAA | 18 | a0001c0001t0002g0133a0001c0001t0002g0242a0001c0001t0002g0273others(15): Show | 19 | HG01123.hp2 HG01256.hp2 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.2310+3011_2310+301 others(6): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220179244 | ||||||
| chr1:220179244
|
CA | C | 13 | a0001c0001t0001g0059a0001c0001t0001g0107a0001c0001t0001g0128others(10): Show | 13 | HG01069.hp1 HG01516.hp2 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.2310+3012delT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220179244 | ||||||
| chr1:220179244
|
CAAAAAAA others(2): Show |
C | 5 | a0002c0002t0008g0001a0002c0002t0008g0003a0002c0002t0008g0019others(2): Show | 8 | HG00558.hp1 HG03688.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.2310+3004_2310+301 others(13): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220179244 | ||||||
| chr1:220179329
|
TAGTA | T | 5 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0272others(2): Show | 5 | HG02602.hp1 NA18948.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.2310+2924_2310+292 others(8): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220179329 | ||||||
| chr1:220179353
|
A | G | 20 | a0001c0001t0005g0152a0003c0003t0002g0037a0003c0003t0002g0043others(17): Show | 20 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.2310+2904T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220179353 | ||||||
| chr1:220179361
|
C | T | 5 | a0002c0002t0008g0001a0002c0002t0008g0003a0002c0002t0008g0019others(2): Show | 8 | HG00558.hp1 HG03688.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.2310+2896G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220179361 | ||||||
| chr1:220179870
|
A | C | 2 | a0001c0001t0001g0130a0001c0001t0002g0126 | 2 | HG00735.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.2310+2387T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220179870 | ||||||
| chr1:220179902
|
G | A | 19 | a0003c0003t0002g0037a0003c0003t0002g0043a0003c0003t0002g0053others(16): Show | 19 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.2310+2355C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220179902 | ||||||
| chr1:220179959
|
C | T | 2 | a0001c0001t0017g0216a0001c0001t0017g0217 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2310+2298G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220179959 | ||||||
| chr1:220180110
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2310+2147G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220180110 | ||||||
| chr1:220180155
|
C | T | 1 | a0001c0001t0001g0149 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2310+2102G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220180155 | ||||||
| chr1:220180289
|
T | C | 138 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(135): Show | 140 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.2310+1968A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220180289 | ||||||
| chr1:220180338
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2310+1919G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220180338 | ||||||
| chr1:220180476
|
T | C | 4 | a0001c0001t0013g0219a0001c0001t0013g0220a0001c0001t0013g0221others(1): Show | 4 | HG02055.hp2 HG02723.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2310+1781A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220180476 | ||||||
| chr1:220180954
|
T | C | 1 | a0001c0001t0002g0071 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2310+1303A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220180954 | ||||||
| chr1:220181034
|
C | G | 4 | a0001c0001t0002g0235a0001c0001t0002g0350a0001c0001t0022g0209others(1): Show | 4 | HG02258.hp2 HG02559.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2310+1223G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220181034 | ||||||
| chr1:220181074
|
T | C | 1 | a0001c0001t0002g0319 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2310+1183A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220181074 | ||||||
| chr1:220181235
|
C | T | 1 | a0001c0001t0003g0171 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2310+1022G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220181235 | ||||||
| chr1:220181595
|
A | G | 1 | a0001c0001t0001g0261 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2310+662T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220181595 | ||||||
| chr1:220181619
|
GTTT | G | 3 | a0001c0001t0002g0235a0001c0001t0002g0350a0001c0001t0026g0224 | 3 | HG02258.hp2 HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2310+635_2310+637d others(5): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220181619 | ||||||
| chr1:220181738
|
C | T | 4 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0124others(1): Show | 4 | HG02027.hp2 NA18975.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.2310+519G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220181738 | ||||||
| chr1:220181774
|
G | T | 1 | a0001c0001t0002g0316 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2310+483C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220181774 | ||||||
| chr1:220181888
|
A | G | 56 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0247others(53): Show | 56 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.2310+369T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220181888 | ||||||
| chr1:220181912
|
T | A | 1 | a0001c0001t0001g0341 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2310+345A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220181912 | ||||||
| chr1:220182049
|
G | GA | 20 | a0001c0001t0002g0306a0001c0001t0005g0152a0003c0003t0002g0037others(17): Show | 20 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.2310+207dupT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220182049 | ||||||
| chr1:220182091
|
CT | C | 243 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0244others(240): Show | 251 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(248): Show |
intron_variant | MODIFIER | c.2310+165delA | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 21/34 | chr1 | 220182091 | ||||||
| chr1:220182426
|
C | A | 2 | a0001c0001t0017g0216a0001c0001t0017g0217 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2213-72G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 20/34 | chr1 | 220182426 | ||||||
| chr1:220183079
|
C | T | 1 | a0001c0001t0001g0261 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1999-148G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 19/34 | chr1 | 220183079 | ||||||
| chr1:220183205
|
T | C | 1 | a0001c0001t0033g0255 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1999-274A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 19/34 | chr1 | 220183205 | ||||||
| chr1:220183250
|
A | AT | 21 | a0001c0001t0001g0079a0001c0001t0002g0273a0001c0001t0003g0080others(18): Show | 21 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.1999-320dupA | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 19/34 | chr1 | 220183250 | ||||||
| chr1:220183250
|
A | T | 4 | a0001c0001t0002g0235a0001c0001t0002g0350a0001c0001t0022g0209others(1): Show | 4 | HG02258.hp2 HG02559.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1999-319T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 19/34 | chr1 | 220183250 | ||||||
| chr1:220183251
|
T | A | 3 | a0002c0002t0007g0004a0002c0002t0007g0022a0002c0002t0007g0023 | 4 | HG00423.hp1 NA18954.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1999-320A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 19/34 | chr1 | 220183251 | ||||||
| chr1:220183369
|
C | A | 2 | a0002c0002t0007g0022a0002c0002t0007g0023 | 2 | HG00423.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1999-438G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 19/34 | chr1 | 220183369 | ||||||
| chr1:220183423
|
T | A | 1 | a0001c0001t0004g0322 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1999-492A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 19/34 | chr1 | 220183423 | ||||||
| chr1:220183484
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1998+552G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 19/34 | chr1 | 220183484 | ||||||
| chr1:220183619
|
C | T | 1 | a0001c0001t0003g0176 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1998+417G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 19/34 | chr1 | 220183619 | ||||||
| chr1:220183681
|
G | A | 1 | a0007c0013t0001g0150 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1998+355C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 19/34 | chr1 | 220183681 | ||||||
| chr1:220183705
|
A | G | 2 | a0001c0001t0017g0216a0001c0001t0017g0217 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1998+331T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 19/34 | chr1 | 220183705 | ||||||
| chr1:220183959
|
T | C | 22 | a0001c0001t0005g0152a0001c0001t0017g0216a0001c0001t0017g0217others(19): Show | 22 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1998+77A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 19/34 | chr1 | 220183959 | ||||||
| chr1:220183964
|
T | C | 1 | a0001c0001t0001g0153 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1998+72A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 19/34 | chr1 | 220183964 | ||||||
| chr1:220184203
|
T | A | 1 | a0007c0013t0001g0150 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1871-40A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 18/34 | chr1 | 220184203 | ||||||
| chr1:220184504
|
A | G | 14 | a0001c0001t0005g0152a0003c0003t0002g0053a0003c0003t0002g0054others(11): Show | 14 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.1871-341T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 18/34 | chr1 | 220184504 | ||||||
| chr1:220184584
|
A | G | 1 | a0001c0001t0001g0261 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1871-421T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 18/34 | chr1 | 220184584 | ||||||
| chr1:220184714
|
T | C | 1 | a0001c0014t0001g0269 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1871-551A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 18/34 | chr1 | 220184714 | ||||||
| chr1:220185180
|
G | A | 20 | a0001c0001t0005g0152a0003c0003t0002g0037a0003c0003t0002g0043others(17): Show | 20 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.1870+471C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 18/34 | chr1 | 220185180 | ||||||
| chr1:220185602
|
C | A | 1 | a0001c0001t0003g0168 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1870+49G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 18/34 | chr1 | 220185602 | ||||||
| chr1:220185895
|
G | T | 5 | a0001c0001t0001g0185a0001c0001t0005g0096a0001c0001t0005g0099others(2): Show | 5 | HG01346.hp1 HG01433.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.1780-154C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220185895 | ||||||
| chr1:220186005
|
T | C | 49 | a0001c0001t0002g0181a0001c0001t0002g0205a0001c0001t0002g0206others(46): Show | 51 | HG00544.hp1 HG00558.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.1780-264A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220186005 | ||||||
| chr1:220186109
|
T | G | 1 | a0001c0001t0002g0290 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1780-368A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220186109 | ||||||
| chr1:220186401
|
G | T | 55 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0247others(52): Show | 55 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.1780-660C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220186401 | ||||||
| chr1:220186403
|
G | A | 55 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0247others(52): Show | 55 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.1780-662C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220186403 | ||||||
| chr1:220186441
|
C | T | 1 | a0001c0001t0012g0314 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1780-700G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220186441 | ||||||
| chr1:220186455
|
A | G | 1 | a0001c0001t0003g0169 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1780-714T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220186455 | ||||||
| chr1:220186470
|
G | A | 1 | a0001c0001t0001g0363 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1780-729C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220186470 | ||||||
| chr1:220186499
|
A | G | 1 | a0003c0003t0006g0046 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1780-758T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220186499 | ||||||
| chr1:220186551
|
C | G | 2 | a0001c0001t0004g0259a0001c0001t0004g0260 | 2 | HG00423.hp2 HG00597.hp2 |
intron_variant | MODIFIER | c.1780-810G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220186551 | ||||||
| chr1:220186648
|
T | C | 1 | a0001c0001t0004g0331 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1780-907A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220186648 | ||||||
| chr1:220186760
|
C | A | 1 | a0001c0001t0001g0134 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1780-1019G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220186760 | ||||||
| chr1:220186770
|
A | G | 1 | a0001c0017t0001g0234 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1780-1029T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220186770 | ||||||
| chr1:220186796
|
T | A | 2 | a0003c0003t0002g0037a0003c0003t0002g0043 | 2 | HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1780-1055A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220186796 | ||||||
| chr1:220186855
|
A | T | 2 | a0001c0001t0002g0061a0001c0001t0002g0082 | 2 | HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1780-1114T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220186855 | ||||||
| chr1:220187064
|
T | G | 1 | a0001c0001t0001g0088 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1780-1323A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220187064 | ||||||
| chr1:220187353
|
A | AC | 20 | a0001c0001t0005g0152a0003c0003t0002g0037a0003c0003t0002g0043others(17): Show | 20 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.1780-1613dupG | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220187353 | ||||||
| chr1:220187699
|
G | T | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1780-1958C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220187699 | ||||||
| chr1:220187864
|
A | G | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1779+1839T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220187864 | ||||||
| chr1:220188104
|
G | GA | 66 | a0001c0001t0001g0026a0001c0001t0001g0134a0001c0001t0001g0151others(63): Show | 66 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.1779+1598dupT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220188104 | ||||||
| chr1:220188105
|
A | G | 20 | a0001c0001t0005g0152a0003c0003t0002g0037a0003c0003t0002g0043others(17): Show | 20 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.1779+1598T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220188105 | ||||||
| chr1:220188302
|
A | G | 113 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0247others(110): Show | 119 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.1779+1401T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220188302 | ||||||
| chr1:220188396
|
A | C | 1 | a0001c0001t0014g0246 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1779+1307T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220188396 | ||||||
| chr1:220188455
|
G | C | 20 | a0001c0001t0005g0152a0003c0003t0002g0037a0003c0003t0002g0043others(17): Show | 20 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.1779+1248C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220188455 | ||||||
| chr1:220188476
|
G | A | 2 | a0001c0001t0015g0339a0001c0001t0015g0340 | 2 | HG01261.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1779+1227C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220188476 | ||||||
| chr1:220188546
|
A | G | 6 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0213others(3): Show | 6 | HG01891.hp2 HG02630.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1779+1157T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220188546 | ||||||
| chr1:220188570
|
G | A | 1 | a0001c0001t0002g0279 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1779+1133C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220188570 | ||||||
| chr1:220188688
|
G | A | 2 | a0003c0003t0002g0037a0003c0003t0002g0043 | 2 | HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1779+1015C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220188688 | ||||||
| chr1:220188806
|
G | A | 2 | a0001c0001t0009g0346a0001c0001t0009g0347 | 2 | HG02109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1779+897C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220188806 | ||||||
| chr1:220189105
|
G | C | 69 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0247others(66): Show | 70 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.1779+598C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220189105 | ||||||
| chr1:220189117
|
G | A | 20 | a0001c0001t0005g0152a0003c0003t0002g0037a0003c0003t0002g0043others(17): Show | 20 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.1779+586C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220189117 | ||||||
| chr1:220189159
|
G | A | 1 | a0001c0001t0002g0276 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1779+544C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220189159 | ||||||
| chr1:220189365
|
C | G | 59 | a0001c0001t0002g0071a0001c0001t0002g0133a0001c0001t0002g0242others(56): Show | 59 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.1779+338G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220189365 | ||||||
| chr1:220189440
|
C | T | 48 | a0001c0001t0002g0181a0001c0001t0002g0205a0001c0001t0002g0206others(45): Show | 50 | HG00544.hp1 HG00558.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1779+263G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220189440 | ||||||
| chr1:220189478
|
C | G | 1 | a0002c0002t0007g0013 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1779+225G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220189478 | ||||||
| chr1:220189515
|
AT | A | 279 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(276): Show | 282 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(279): Show |
intron_variant | MODIFIER | c.1779+187delA | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220189515 | ||||||
| chr1:220189515
|
ATT | A | 35 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0111others(32): Show | 40 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.1779+186_1779+187d others(4): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220189515 | ||||||
| chr1:220189527
|
T | C | 3 | a0001c0001t0002g0133a0001c0001t0002g0294a0001c0001t0004g0333 | 3 | HG01978.hp2 HG02148.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.1779+176A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220189527 | ||||||
| chr1:220189696
|
C | T | 3 | a0001c0001t0002g0235a0001c0001t0002g0350a0001c0001t0026g0224 | 3 | HG02258.hp2 HG02559.hp2 NA21309.hp2 |
splice_region_variant&intron_variant | LOW | c.1779+7G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 17/34 | chr1 | 220189696 | ||||||
| chr1:220190162
|
T | C | 2 | a0001c0001t0003g0358a0001c0001t0003g0359 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1632-16A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 15/34 | chr1 | 220190162 | ||||||
| chr1:220190612
|
T | C | 1 | a0001c0001t0001g0261 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1488-92A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 14/34 | chr1 | 220190612 | ||||||
| chr1:220190740
|
CCT | C | 4 | a0003c0003t0006g0038a0003c0003t0006g0041a0003c0003t0006g0042others(1): Show | 4 | HG02004.hp2 HG02886.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1488-222_1488-221d others(4): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 14/34 | chr1 | 220190740 | ||||||
| chr1:220190791
|
G | C | 1 | a0001c0001t0001g0147 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1488-271C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 14/34 | chr1 | 220190791 | ||||||
| chr1:220190792
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1488-272C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 14/34 | chr1 | 220190792 | ||||||
| chr1:220190818
|
C | A | 4 | a0001c0001t0013g0219a0001c0001t0013g0220a0001c0001t0013g0221others(1): Show | 4 | HG02055.hp2 HG02723.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1487+250G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 14/34 | chr1 | 220190818 | ||||||
| chr1:220191508
|
C | T | 18 | a0002c0002t0007g0002a0002c0002t0007g0004a0002c0002t0007g0009others(15): Show | 23 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.1271-224G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 13/34 | chr1 | 220191508 | ||||||
| chr1:220191635
|
G | A | 338 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(335): Show | 346 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(343): Show |
intron_variant | MODIFIER | c.1271-351C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 13/34 | chr1 | 220191635 | ||||||
| chr1:220191687
|
G | A | 5 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0004g0034others(2): Show | 5 | HG02922.hp2 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1271-403C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 13/34 | chr1 | 220191687 | ||||||
| chr1:220191773
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1271-489C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 13/34 | chr1 | 220191773 | ||||||
| chr1:220191804
|
G | A | 1 | a0001c0001t0004g0326 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1271-520C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 13/34 | chr1 | 220191804 | ||||||
| chr1:220191805
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1271-521G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 13/34 | chr1 | 220191805 | ||||||
| chr1:220191828
|
A | G | 2 | a0001c0001t0002g0211a0001c0001t0014g0210 | 2 | HG01891.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1271-544T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 13/34 | chr1 | 220191828 | ||||||
| chr1:220191856
|
G | A | 1 | a0002c0002t0007g0013 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1271-572C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 13/34 | chr1 | 220191856 | ||||||
| chr1:220191860
|
C | T | 2 | a0003c0003t0002g0037a0003c0003t0002g0043 | 2 | HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1271-576G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 13/34 | chr1 | 220191860 | ||||||
| chr1:220191906
|
C | CTT | 4 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0214others(1): Show | 4 | HG02630.hp2 HG03130.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1271-624_1271-623d others(4): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 13/34 | chr1 | 220191906 | ||||||
| chr1:220191969
|
G | C | 1 | a0003c0003t0006g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1271-685C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 13/34 | chr1 | 220191969 | ||||||
| chr1:220191982
|
T | A | 116 | a0001c0001t0001g0185a0001c0001t0002g0030a0001c0001t0002g0031others(113): Show | 118 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.1271-698A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 13/34 | chr1 | 220191982 | ||||||
| chr1:220192029
|
T | G | 1 | a0001c0001t0014g0246 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1271-745A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 13/34 | chr1 | 220192029 | ||||||
| chr1:220192100
|
G | A | 1 | a0001c0001t0001g0341 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1271-816C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 13/34 | chr1 | 220192100 | ||||||
| chr1:220192250
|
C | T | 1 | a0001c0001t0029g0117 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1271-966G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 13/34 | chr1 | 220192250 | ||||||
| chr1:220192359
|
CCATT | C | 243 | a0001c0001t0001g0064a0001c0001t0001g0185a0001c0001t0001g0228others(240): Show | 251 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(248): Show |
intron_variant | MODIFIER | c.1270+877_1270+880d others(6): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 13/34 | chr1 | 220192359 | ||||||
| chr1:220192633
|
G | C | 15 | a0002c0002t0007g0002a0002c0002t0007g0009a0002c0002t0007g0010others(12): Show | 19 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.1270+607C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 13/34 | chr1 | 220192633 | ||||||
| chr1:220192758
|
A | G | 18 | a0002c0002t0007g0002a0002c0002t0007g0004a0002c0002t0007g0009others(15): Show | 23 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.1270+482T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 13/34 | chr1 | 220192758 | ||||||
| chr1:220192821
|
T | C | 1 | a0001c0001t0004g0227 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1270+419A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 13/34 | chr1 | 220192821 | ||||||
| chr1:220193155
|
T | A | 18 | a0002c0002t0007g0002a0002c0002t0007g0004a0002c0002t0007g0009others(15): Show | 23 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.1270+85A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 13/34 | chr1 | 220193155 | ||||||
| chr1:220193445
|
C | T | 2 | a0001c0001t0003g0192a0001c0001t0008g0075 | 2 | NA19004.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1131-66G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 12/34 | chr1 | 220193445 | ||||||
| chr1:220193547
|
T | C | 1 | a0001c0001t0001g0361 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1131-168A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 12/34 | chr1 | 220193547 | ||||||
| chr1:220193604
|
C | T | 18 | a0002c0002t0007g0002a0002c0002t0007g0004a0002c0002t0007g0009others(15): Show | 23 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.1131-225G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 12/34 | chr1 | 220193604 | ||||||
| chr1:220193718
|
C | T | 18 | a0002c0002t0007g0002a0002c0002t0007g0004a0002c0002t0007g0009others(15): Show | 23 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.1131-339G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 12/34 | chr1 | 220193718 | ||||||
| chr1:220193953
|
C | T | 1 | a0001c0001t0003g0201 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1131-574G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 12/34 | chr1 | 220193953 | ||||||
| chr1:220194098
|
A | C | 1 | a0001c0001t0001g0107 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1131-719T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 12/34 | chr1 | 220194098 | ||||||
| chr1:220194365
|
A | G | 1 | a0001c0001t0003g0193 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1130+713T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 12/34 | chr1 | 220194365 | ||||||
| chr1:220194491
|
T | C | 1 | a0001c0017t0001g0234 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1130+587A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 12/34 | chr1 | 220194491 | ||||||
| chr1:220194504
|
T | G | 1 | a0001c0001t0015g0340 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1130+574A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 12/34 | chr1 | 220194504 | ||||||
| chr1:220194682
|
C | T | 1 | a0001c0001t0003g0243 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1130+396G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 12/34 | chr1 | 220194682 | ||||||
| chr1:220194706
|
T | A | 2 | a0001c0001t0002g0350a0001c0001t0004g0333 | 2 | HG02258.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.1130+372A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 12/34 | chr1 | 220194706 | ||||||
| chr1:220194741
|
C | T | 1 | a0001c0001t0012g0267 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1130+337G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 12/34 | chr1 | 220194741 | ||||||
| chr1:220194964
|
G | A | 1 | a0001c0001t0002g0212 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1130+114C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 12/34 | chr1 | 220194964 | ||||||
| chr1:220195185
|
T | G | 20 | a0001c0001t0005g0152a0003c0003t0002g0037a0003c0003t0002g0043others(17): Show | 20 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.1041-18A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 11/34 | chr1 | 220195185 | ||||||
| chr1:220195209
|
G | C | 1 | a0001c0001t0001g0086 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1041-42C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 11/34 | chr1 | 220195209 | ||||||
| chr1:220195695
|
C | T | 43 | a0001c0001t0002g0235a0001c0001t0002g0350a0001c0001t0017g0216others(40): Show | 48 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.961-318G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 10/34 | chr1 | 220195695 | ||||||
| chr1:220196067
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.960+183A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 10/34 | chr1 | 220196067 | ||||||
| chr1:220196400
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG03041.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.812-2A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220196400 | ||||||
| chr1:220196403
|
TA | T | 118 | a0001c0001t0001g0064a0001c0001t0001g0185a0001c0001t0002g0030others(115): Show | 120 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(117): Show |
splice_region_variant&intron_variant | LOW | c.812-6delT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220196403 | ||||||
| chr1:220196551
|
G | T | 5 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(2): Show | 5 | HG02109.hp1 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.812-153C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220196551 | ||||||
| chr1:220196659
|
C | T | 2 | a0001c0001t0001g0244a0001c0001t0001g0261 | 2 | HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.812-261G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220196659 | ||||||
| chr1:220196674
|
T | C | 4 | a0001c0001t0002g0235a0001c0001t0002g0350a0001c0001t0022g0209others(1): Show | 4 | HG02258.hp2 HG02559.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.812-276A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220196674 | ||||||
| chr1:220196786
|
A | G | 364 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(361): Show | 372 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(369): Show |
intron_variant | MODIFIER | c.812-388T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220196786 | ||||||
| chr1:220196792
|
A | G | 1 | a0001c0001t0034g0370 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.812-394T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220196792 | ||||||
| chr1:220196857
|
AAATTTCC others(6): Show |
A | 3 | a0002c0002t0008g0001a0002c0002t0008g0003a0002c0002t0008g0019 | 6 | NA18942.hp1 NA18973.hp1 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.812-472_812-460del others(13): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220196857 | ||||||
| chr1:220196979
|
A | G | 2 | a0001c0001t0011g0351a0001c0001t0011g0352 | 2 | HG01243.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.812-581T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220196979 | ||||||
| chr1:220197133
|
G | A | 1 | a0001c0004t0009g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.812-735C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220197133 | ||||||
| chr1:220197134
|
C | T | 1 | a0001c0001t0014g0246 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.812-736G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220197134 | ||||||
| chr1:220197295
|
G | A | 13 | a0001c0001t0001g0341a0001c0001t0009g0343a0001c0001t0009g0344others(10): Show | 14 | HG01433.hp1 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.812-897C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220197295 | ||||||
| chr1:220197299
|
G | A | 1 | a0001c0001t0003g0169 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.812-901C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220197299 | ||||||
| chr1:220197324
|
A | T | 39 | a0001c0001t0017g0216a0001c0001t0017g0217a0002c0002t0007g0002others(36): Show | 44 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.812-926T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220197324 | ||||||
| chr1:220197337
|
A | G | 39 | a0001c0001t0017g0216a0001c0001t0017g0217a0002c0002t0007g0002others(36): Show | 44 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.812-939T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220197337 | ||||||
| chr1:220197341
|
TTCAG | T | 39 | a0001c0001t0017g0216a0001c0001t0017g0217a0002c0002t0007g0002others(36): Show | 44 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.812-947_812-944del others(4): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220197341 | ||||||
| chr1:220197654
|
A | G | 367 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(364): Show | 375 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(372): Show |
intron_variant | MODIFIER | c.812-1256T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220197654 | ||||||
| chr1:220197778
|
T | A | 22 | a0001c0001t0001g0341a0001c0001t0002g0211a0001c0001t0002g0212others(19): Show | 23 | HG01261.hp2 HG01433.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.812-1380A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220197778 | ||||||
| chr1:220197802
|
G | A | 1 | a0001c0001t0005g0249 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.812-1404C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220197802 | ||||||
| chr1:220197835
|
T | C | 1 | a0001c0001t0002g0310 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.812-1437A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220197835 | ||||||
| chr1:220197883
|
A | G | 12 | a0001c0001t0002g0133a0001c0001t0002g0294a0001c0001t0002g0302others(9): Show | 12 | HG00408.hp2 HG01978.hp2 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.812-1485T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220197883 | ||||||
| chr1:220197980
|
C | G | 1 | a0001c0001t0018g0073 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.812-1582G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220197980 | ||||||
| chr1:220198054
|
C | T | 1 | a0001c0001t0002g0291 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.812-1656G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220198054 | ||||||
| chr1:220198160
|
G | A | 3 | a0002c0002t0008g0001a0002c0002t0008g0003a0002c0002t0008g0019 | 6 | NA18942.hp1 NA18973.hp1 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.812-1762C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220198160 | ||||||
| chr1:220198167
|
C | T | 12 | a0001c0001t0009g0343a0001c0001t0009g0344a0001c0001t0009g0346others(9): Show | 13 | HG01433.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.812-1769G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220198167 | ||||||
| chr1:220198184
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.812-1786G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220198184 | ||||||
| chr1:220198362
|
C | T | 18 | a0002c0002t0007g0002a0002c0002t0007g0004a0002c0002t0007g0009others(15): Show | 23 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.812-1964G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220198362 | ||||||
| chr1:220198527
|
C | T | 3 | a0001c0001t0005g0096a0001c0001t0005g0099a0001c0001t0005g0154 | 3 | HG01433.hp2 HG03704.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.812-2129G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220198527 | ||||||
| chr1:220198560
|
TG | T | 18 | a0002c0002t0007g0002a0002c0002t0007g0004a0002c0002t0007g0009others(15): Show | 23 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.812-2163delC | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220198560 | ||||||
| chr1:220198688
|
G | C | 2 | a0001c0001t0001g0244a0001c0001t0001g0261 | 2 | HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.812-2290C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220198688 | ||||||
| chr1:220198888
|
C | T | 19 | a0003c0003t0002g0037a0003c0003t0002g0043a0003c0003t0002g0053others(16): Show | 19 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.812-2490G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220198888 | ||||||
| chr1:220199069
|
G | A | 2 | a0001c0001t0004g0034a0001c0001t0004g0035 | 2 | HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.812-2671C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220199069 | ||||||
| chr1:220199133
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.812-2735G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220199133 | ||||||
| chr1:220199207
|
C | T | 20 | a0002c0002t0007g0002a0002c0002t0007g0004a0002c0002t0007g0009others(17): Show | 25 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.812-2809G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220199207 | ||||||
| chr1:220199221
|
T | C | 1 | a0001c0001t0004g0226 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.812-2823A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220199221 | ||||||
| chr1:220199330
|
AT | A | 20 | a0002c0002t0007g0002a0002c0002t0007g0004a0002c0002t0007g0009others(17): Show | 25 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.812-2933delA | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220199330 | ||||||
| chr1:220199331
|
T | C | 1 | a0001c0001t0001g0355 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.812-2933A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220199331 | ||||||
| chr1:220199455
|
T | C | 17 | a0002c0002t0007g0002a0002c0002t0007g0009a0002c0002t0007g0010others(14): Show | 21 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.811+2821A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220199455 | ||||||
| chr1:220199671
|
A | C | 20 | a0002c0002t0007g0002a0002c0002t0007g0004a0002c0002t0007g0009others(17): Show | 25 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.811+2605T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220199671 | ||||||
| chr1:220200137
|
T | A | 55 | a0001c0001t0002g0071a0001c0001t0002g0133a0001c0001t0002g0270others(52): Show | 55 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.811+2139A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220200137 | ||||||
| chr1:220200267
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.811+2009G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220200267 | ||||||
| chr1:220200340
|
T | C | 3 | a0001c0001t0005g0096a0001c0001t0005g0099a0001c0001t0005g0154 | 3 | HG01433.hp2 HG03704.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.811+1936A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220200340 | ||||||
| chr1:220200435
|
T | C | 22 | a0001c0001t0001g0341a0001c0001t0002g0032a0001c0001t0002g0211others(19): Show | 23 | HG01261.hp2 HG01433.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.811+1841A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220200435 | ||||||
| chr1:220200511
|
T | C | 3 | a0001c0001t0004g0237a0001c0001t0004g0238a0001c0001t0004g0239 | 3 | HG02723.hp1 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.811+1765A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220200511 | ||||||
| chr1:220200515
|
C | A | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.811+1761G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220200515 | ||||||
| chr1:220200601
|
C | G | 3 | a0001c0001t0002g0235a0001c0001t0002g0350a0001c0001t0026g0224 | 3 | HG02258.hp2 HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.811+1675G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220200601 | ||||||
| chr1:220200638
|
G | A | 2 | a0001c0001t0003g0192a0001c0001t0008g0075 | 2 | NA19004.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.811+1638C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220200638 | ||||||
| chr1:220200705
|
A | C | 5 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0131others(2): Show | 5 | HG01071.hp1 HG01175.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.811+1571T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220200705 | ||||||
| chr1:220200935
|
T | C | 1 | a0001c0001t0017g0216 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.811+1341A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220200935 | ||||||
| chr1:220201242
|
C | T | 1 | a0001c0001t0003g0192 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.811+1034G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220201242 | ||||||
| chr1:220201340
|
T | C | 4 | a0001c0001t0002g0235a0001c0001t0002g0350a0001c0001t0022g0209others(1): Show | 4 | HG02258.hp2 HG02559.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.811+936A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220201340 | ||||||
| chr1:220201390
|
C | A | 5 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0272others(2): Show | 5 | HG02602.hp1 NA18948.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.811+886G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220201390 | ||||||
| chr1:220201693
|
T | G | 1 | a0001c0001t0017g0217 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.811+583A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220201693 | ||||||
| chr1:220201791
|
T | A | 1 | a0001c0001t0002g0300 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.811+485A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220201791 | ||||||
| chr1:220201798
|
T | C | 232 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(229): Show | 238 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(235): Show |
intron_variant | MODIFIER | c.811+478A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220201798 | ||||||
| chr1:220201973
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.811+303G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220201973 | ||||||
| chr1:220202034
|
G | A | 8 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(5): Show | 8 | HG02109.hp1 HG02258.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.811+242C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220202034 | ||||||
| chr1:220202077
|
A | T | 28 | a0001c0001t0001g0047a0001c0001t0002g0030a0001c0001t0002g0031others(25): Show | 28 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.811+199T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220202077 | ||||||
| chr1:220202118
|
T | C | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.811+158A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 9/34 | chr1 | 220202118 | ||||||
| chr1:220202386
|
A | G | 3 | a0001c0001t0002g0279a0001c0001t0002g0300a0001c0001t0002g0317 | 3 | HG00140.hp2 HG01175.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.713-12T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 8/34 | chr1 | 220202386 | ||||||
| chr1:220202534
|
A | C | 3 | a0001c0001t0005g0136a0001c0001t0005g0137a0008c0015t0005g0140 | 3 | NA18942.hp2 NA18983.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.713-160T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 8/34 | chr1 | 220202534 | ||||||
| chr1:220202543
|
G | A | 1 | a0001c0017t0001g0234 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.713-169C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 8/34 | chr1 | 220202543 | ||||||
| chr1:220202611
|
A | T | 130 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0244others(127): Show | 130 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.713-237T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 8/34 | chr1 | 220202611 | ||||||
| chr1:220202899
|
C | T | 1 | a0001c0001t0004g0258 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.713-525G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 8/34 | chr1 | 220202899 | ||||||
| chr1:220203051
|
G | C | 125 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0244others(122): Show | 125 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.713-677C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 8/34 | chr1 | 220203051 | ||||||
| chr1:220203084
|
C | T | 1 | a0001c0001t0002g0301 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.713-710G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 8/34 | chr1 | 220203084 | ||||||
| chr1:220203222
|
T | G | 23 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0074others(20): Show | 23 | HG01358.hp2 HG01496.hp1 HG01934.hp2 others(20): Show |
intron_variant | MODIFIER | c.713-848A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 8/34 | chr1 | 220203222 | ||||||
| chr1:220203331
|
G | C | 27 | a0001c0001t0001g0047a0001c0001t0002g0030a0001c0001t0002g0031others(24): Show | 27 | HG00609.hp2 HG00621.hp1 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.713-957C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 8/34 | chr1 | 220203331 | ||||||
| chr1:220203388
|
T | A | 2 | a0001c0001t0017g0216a0001c0001t0017g0217 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.713-1014A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 8/34 | chr1 | 220203388 | ||||||
| chr1:220203609
|
T | G | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.713-1235A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 8/34 | chr1 | 220203609 | ||||||
| chr1:220203719
|
G | A | 12 | a0001c0001t0001g0341a0001c0001t0009g0343a0001c0001t0009g0344others(9): Show | 13 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.713-1345C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 8/34 | chr1 | 220203719 | ||||||
| chr1:220203879
|
A | T | 1 | a0001c0001t0004g0334 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.713-1505T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 8/34 | chr1 | 220203879 | ||||||
| chr1:220203968
|
A | T | 2 | a0001c0001t0017g0216a0001c0001t0017g0217 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.713-1594T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 8/34 | chr1 | 220203968 | ||||||
| chr1:220203969
|
A | C | 2 | a0001c0001t0017g0216a0001c0001t0017g0217 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.713-1595T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 8/34 | chr1 | 220203969 | ||||||
| chr1:220204088
|
G | A | 27 | a0001c0001t0001g0047a0001c0001t0002g0030a0001c0001t0002g0031others(24): Show | 27 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.713-1714C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 8/34 | chr1 | 220204088 | ||||||
| chr1:220204513
|
G | C | 1 | a0001c0001t0003g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.712+1394C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 8/34 | chr1 | 220204513 | ||||||
| chr1:220204525
|
T | C | 1 | a0010c0018t0003g0207 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.712+1382A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 8/34 | chr1 | 220204525 | ||||||
| chr1:220204530
|
G | C | 8 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(5): Show | 9 | HG00423.hp1 HG02027.hp2 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.712+1377C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 8/34 | chr1 | 220204530 | ||||||
| chr1:220204549
|
A | G | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.712+1358T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 8/34 | chr1 | 220204549 | ||||||
| chr1:220204588
|
A | AT | 18 | a0001c0001t0017g0216a0001c0001t0017g0217a0002c0002t0007g0002others(15): Show | 22 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.712+1318dupA | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 8/34 | chr1 | 220204588 | ||||||
| chr1:220204588
|
A | ATT | 6 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(3): Show | 7 | HG00423.hp1 HG02027.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.712+1317_712+1318d others(4): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 8/34 | chr1 | 220204588 | ||||||
| chr1:220204674
|
C | T | 1 | a0001c0001t0004g0326 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.712+1233G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 8/34 | chr1 | 220204674 | ||||||
| chr1:220205054
|
A | G | 1 | a0001c0001t0002g0292 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.712+853T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 8/34 | chr1 | 220205054 | ||||||
| chr1:220205149
|
C | T | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.712+758G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 8/34 | chr1 | 220205149 | ||||||
| chr1:220205195
|
T | G | 1 | a0001c0001t0014g0246 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.712+712A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 8/34 | chr1 | 220205195 | ||||||
| chr1:220205263
|
T | C | 1 | a0001c0004t0009g0342 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.712+644A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 8/34 | chr1 | 220205263 | ||||||
| chr1:220205436
|
C | T | 6 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0213others(3): Show | 6 | HG01891.hp2 HG02630.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.712+471G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 8/34 | chr1 | 220205436 | ||||||
| chr1:220205547
|
C | T | 1 | a0001c0001t0004g0226 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.712+360G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 8/34 | chr1 | 220205547 | ||||||
| chr1:220205624
|
C | G | 10 | a0002c0002t0007g0002a0002c0002t0007g0009a0002c0002t0007g0010others(7): Show | 11 | HG00639.hp1 HG01074.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.712+283G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 8/34 | chr1 | 220205624 | ||||||
| chr1:220206161
|
G | C | 206 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(203): Show | 212 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.613-155C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220206161 | ||||||
| chr1:220206213
|
T | G | 2 | a0001c0001t0017g0216a0001c0001t0017g0217 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.613-207A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220206213 | ||||||
| chr1:220206214
|
G | T | 28 | a0001c0001t0001g0047a0001c0001t0002g0030a0001c0001t0002g0031others(25): Show | 28 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.613-208C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220206214 | ||||||
| chr1:220206277
|
T | A | 1 | a0001c0001t0005g0110 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.613-271A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220206277 | ||||||
| chr1:220206357
|
C | T | 5 | a0001c0001t0001g0069a0001c0001t0001g0084a0001c0001t0001g0087others(2): Show | 5 | HG01496.hp1 HG01934.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.613-351G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220206357 | ||||||
| chr1:220206399
|
G | C | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.613-393C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220206399 | ||||||
| chr1:220206537
|
T | C | 21 | a0001c0001t0001g0341a0001c0001t0002g0211a0001c0001t0002g0212others(18): Show | 22 | HG01261.hp2 HG01433.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.613-531A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220206537 | ||||||
| chr1:220206548
|
G | A | 1 | a0001c0001t0002g0213 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.613-542C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220206548 | ||||||
| chr1:220206548
|
G | T | 5 | a0001c0001t0003g0263a0001c0001t0003g0265a0001c0001t0012g0267others(2): Show | 5 | HG01243.hp1 HG03486.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.613-542C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220206548 | ||||||
| chr1:220206872
|
T | C | 2 | a0001c0001t0011g0351a0001c0001t0011g0352 | 2 | HG01243.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.613-866A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220206872 | ||||||
| chr1:220206891
|
T | C | 1 | a0001c0001t0026g0224 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.613-885A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220206891 | ||||||
| chr1:220207014
|
C | T | 1 | a0011c0019t0003g0188 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.613-1008G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220207014 | ||||||
| chr1:220207149
|
T | A | 28 | a0001c0001t0001g0047a0001c0001t0002g0030a0001c0001t0002g0031others(25): Show | 28 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.613-1143A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220207149 | ||||||
| chr1:220207291
|
C | T | 21 | a0001c0001t0001g0341a0001c0001t0002g0211a0001c0001t0002g0212others(18): Show | 22 | HG01261.hp2 HG01433.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.613-1285G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220207291 | ||||||
| chr1:220207370
|
C | A | 1 | a0001c0001t0026g0224 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.613-1364G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220207370 | ||||||
| chr1:220207477
|
A | C | 59 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(56): Show | 59 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.613-1471T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220207477 | ||||||
| chr1:220207559
|
C | A | 1 | a0001c0001t0004g0321 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.613-1553G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220207559 | ||||||
| chr1:220207785
|
G | A | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.613-1779C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220207785 | ||||||
| chr1:220207925
|
T | C | 5 | a0001c0001t0003g0263a0001c0001t0003g0265a0001c0001t0012g0267others(2): Show | 5 | HG01243.hp1 HG03486.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.613-1919A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220207925 | ||||||
| chr1:220207948
|
G | A | 1 | a0001c0001t0016g0173 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.613-1942C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220207948 | ||||||
| chr1:220208056
|
A | G | 5 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0131others(2): Show | 5 | HG01071.hp1 HG01175.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.613-2050T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220208056 | ||||||
| chr1:220208116
|
T | G | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.613-2110A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220208116 | ||||||
| chr1:220208278
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.612+2110A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220208278 | ||||||
| chr1:220208351
|
G | A | 1 | a0001c0001t0003g0266 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.612+2037C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220208351 | ||||||
| chr1:220208354
|
G | A | 6 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(3): Show | 7 | HG00423.hp1 HG02027.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.612+2034C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220208354 | ||||||
| chr1:220208415
|
T | C | 1 | a0003c0003t0006g0051 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.612+1973A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220208415 | ||||||
| chr1:220208499
|
T | C | 14 | a0001c0001t0001g0047a0003c0003t0002g0053a0003c0003t0002g0054others(11): Show | 14 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.612+1889A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220208499 | ||||||
| chr1:220208720
|
AT | A | 13 | a0001c0001t0004g0226a0001c0001t0004g0253a0001c0001t0009g0343others(10): Show | 14 | HG01433.hp1 HG01884.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.612+1667delA | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220208720 | ||||||
| chr1:220208756
|
G | A | 54 | a0001c0001t0002g0071a0001c0001t0002g0133a0001c0001t0002g0270others(51): Show | 54 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.612+1632C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220208756 | ||||||
| chr1:220208857
|
C | T | 6 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(3): Show | 7 | HG00423.hp1 HG02027.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.612+1531G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220208857 | ||||||
| chr1:220208877
|
C | T | 28 | a0001c0001t0001g0047a0001c0001t0002g0030a0001c0001t0002g0031others(25): Show | 28 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.612+1511G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220208877 | ||||||
| chr1:220208959
|
C | T | 6 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(3): Show | 7 | HG00423.hp1 HG02027.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.612+1429G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220208959 | ||||||
| chr1:220208972
|
C | G | 2 | a0001c0001t0017g0216a0001c0001t0017g0217 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.612+1416G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220208972 | ||||||
| chr1:220209007
|
G | A | 1 | a0001c0001t0004g0035 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.612+1381C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220209007 | ||||||
| chr1:220209317
|
A | G | 1 | a0001c0001t0004g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.612+1071T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220209317 | ||||||
| chr1:220209342
|
T | C | 1 | a0001c0001t0002g0350 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.612+1046A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220209342 | ||||||
| chr1:220209354
|
C | T | 4 | a0001c0001t0002g0280a0001c0001t0002g0288a0001c0001t0002g0289others(1): Show | 4 | NA18984.hp2 NA18988.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.612+1034G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220209354 | ||||||
| chr1:220209404
|
T | C | 16 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0003g0241others(13): Show | 16 | HG00423.hp2 HG00597.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.612+984A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220209404 | ||||||
| chr1:220209558
|
A | G | 4 | a0001c0001t0001g0247a0001c0001t0004g0218a0001c0001t0004g0256others(1): Show | 4 | HG00735.hp1 HG01109.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.612+830T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220209558 | ||||||
| chr1:220209631
|
G | A | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.612+757C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220209631 | ||||||
| chr1:220209735
|
C | T | 1 | a0001c0001t0034g0370 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.612+653G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220209735 | ||||||
| chr1:220209787
|
G | A | 1 | a0001c0001t0004g0226 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.612+601C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220209787 | ||||||
| chr1:220209804
|
A | G | 1 | a0001c0001t0004g0251 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.612+584T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220209804 | ||||||
| chr1:220209840
|
T | G | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG00621.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.612+548A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220209840 | ||||||
| chr1:220209956
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.612+432C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220209956 | ||||||
| chr1:220210005
|
T | C | 57 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0247others(54): Show | 57 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.612+383A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220210005 | ||||||
| chr1:220210107
|
C | G | 208 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(205): Show | 214 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(211): Show |
intron_variant | MODIFIER | c.612+281G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220210107 | ||||||
| chr1:220210271
|
G | A | 1 | a0001c0001t0002g0298 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.612+117C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 7/34 | chr1 | 220210271 | ||||||
| chr1:220210522
|
T | C | 1 | a0001c0001t0004g0325 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.511-33A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 6/34 | chr1 | 220210522 | ||||||
| chr1:220211020
|
A | T | 1 | a0001c0001t0001g0098 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.387-18T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 4/34 | chr1 | 220211020 | ||||||
| chr1:220211028
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.387-26G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 4/34 | chr1 | 220211028 | ||||||
| chr1:220211343
|
T | A | 1 | a0001c0001t0001g0098 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.387-341A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 4/34 | chr1 | 220211343 | ||||||
| chr1:220211453
|
C | T | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129 | 3 | HG01516.hp2 HG03486.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.387-451G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 4/34 | chr1 | 220211453 | ||||||
| chr1:220211461
|
A | T | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.387-459T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 4/34 | chr1 | 220211461 | ||||||
| chr1:220211523
|
A | G | 1 | a0001c0001t0005g0356 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.387-521T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 4/34 | chr1 | 220211523 | ||||||
| chr1:220211593
|
T | C | 1 | a0001c0001t0011g0351 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.387-591A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 4/34 | chr1 | 220211593 | ||||||
| chr1:220212019
|
G | C | 4 | a0001c0001t0002g0235a0001c0001t0002g0350a0001c0001t0022g0209others(1): Show | 4 | HG02258.hp2 HG02559.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.386+868C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 4/34 | chr1 | 220212019 | ||||||
| chr1:220212101
|
C | T | 125 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0244others(122): Show | 125 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.386+786G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 4/34 | chr1 | 220212101 | ||||||
| chr1:220212211
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.386+676G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 4/34 | chr1 | 220212211 | ||||||
| chr1:220212329
|
G | A | 1 | a0001c0001t0003g0198 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.386+558C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 4/34 | chr1 | 220212329 | ||||||
| chr1:220212397
|
T | C | 1 | a0001c0001t0003g0196 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.386+490A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 4/34 | chr1 | 220212397 | ||||||
| chr1:220212499
|
A | T | 2 | a0001c0001t0017g0216a0001c0001t0017g0217 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.386+388T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 4/34 | chr1 | 220212499 | ||||||
| chr1:220212500
|
T | A | 27 | a0001c0001t0001g0047a0001c0001t0002g0030a0001c0001t0002g0031others(24): Show | 27 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.386+387A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 4/34 | chr1 | 220212500 | ||||||
| chr1:220212501
|
T | TA | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.386+385_386+386ins others(1): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 4/34 | chr1 | 220212501 | ||||||
| chr1:220212643
|
G | A | 1 | a0001c0001t0001g0341 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.386+244C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 4/34 | chr1 | 220212643 | ||||||
| chr1:220213150
|
C | T | 1 | a0001c0001t0003g0196 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.305-182G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 3/34 | chr1 | 220213150 | ||||||
| chr1:220213246
|
C | T | 60 | a0001c0001t0001g0244a0001c0001t0002g0071a0001c0001t0002g0133others(57): Show | 60 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.305-278G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 3/34 | chr1 | 220213246 | ||||||
| chr1:220213365
|
C | T | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.305-397G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 3/34 | chr1 | 220213365 | ||||||
| chr1:220213526
|
T | C | 60 | a0001c0001t0001g0244a0001c0001t0002g0071a0001c0001t0002g0133others(57): Show | 60 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.304+330A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 3/34 | chr1 | 220213526 | ||||||
| chr1:220213730
|
G | GT | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.304+125dupA | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 3/34 | chr1 | 220213730 | ||||||
| chr1:220213732
|
T | TG | 107 | a0001c0001t0001g0059a0001c0001t0001g0062a0001c0001t0001g0064others(104): Show | 107 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.304+123dupC | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 3/34 | chr1 | 220213732 | ||||||
| chr1:220213732
|
TG | T | 37 | a0001c0001t0001g0047a0001c0001t0001g0089a0001c0001t0001g0119others(34): Show | 38 | HG00140.hp1 HG00609.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.304+123delC | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 3/34 | chr1 | 220213732 | ||||||
| chr1:220213735
|
G | A | 16 | a0002c0002t0007g0002a0002c0002t0007g0009a0002c0002t0007g0010others(13): Show | 20 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.304+121C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 3/34 | chr1 | 220213735 | ||||||
| chr1:220213737
|
G | C | 1 | a0001c0001t0002g0318 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.304+119C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 3/34 | chr1 | 220213737 | ||||||
| chr1:220213737
|
G | T | 1 | a0001c0001t0002g0206 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.304+119C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 3/34 | chr1 | 220213737 | ||||||
| chr1:220213740
|
G | A | 10 | a0002c0002t0007g0002a0002c0002t0007g0009a0002c0002t0007g0010others(7): Show | 11 | HG00639.hp1 HG01074.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.304+116C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 3/34 | chr1 | 220213740 | ||||||
| chr1:220213740
|
G | C | 3 | a0001c0001t0001g0247a0001c0001t0004g0218a0001c0001t0004g0256 | 3 | HG01109.hp1 HG03453.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.304+116C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 3/34 | chr1 | 220213740 | ||||||
| chr1:220213741
|
G | A | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.304+115C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 3/34 | chr1 | 220213741 | ||||||
| chr1:220213743
|
G | A | 1 | a0001c0020t0009g0368 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.304+113C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 3/34 | chr1 | 220213743 | ||||||
| chr1:220213743
|
G | GAGA | 15 | a0001c0001t0001g0341a0001c0001t0002g0211a0001c0001t0002g0212others(12): Show | 16 | HG01433.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.304+112_304+113ins others(3): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 3/34 | chr1 | 220213743 | ||||||
| chr1:220213831
|
T | A | 6 | a0003c0003t0002g0053a0003c0003t0003g0057a0003c0003t0006g0045others(3): Show | 6 | HG00621.hp1 HG02165.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.304+25A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 3/34 | chr1 | 220213831 | ||||||
| chr1:220214130
|
T | G | 1 | a0001c0001t0002g0040 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.181-151A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214130 | ||||||
| chr1:220214263
|
T | C | 43 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0341others(40): Show | 49 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.181-284A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214263 | ||||||
| chr1:220214376
|
A | G | 1 | a0001c0001t0017g0217 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.181-397T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214376 | ||||||
| chr1:220214381
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.181-402G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214381 | ||||||
| chr1:220214391
|
C | T | 1 | a0001c0014t0001g0269 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.181-412G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214391 | ||||||
| chr1:220214394
|
C | T | 1 | a0007c0013t0001g0150 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.181-415G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214394 | ||||||
| chr1:220214395
|
G | A | 2 | a0003c0003t0002g0037a0003c0003t0002g0043 | 2 | HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.181-416C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214395 | ||||||
| chr1:220214470
|
G | T | 1 | a0001c0001t0005g0249 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.181-491C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214470 | ||||||
| chr1:220214752
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.181-773A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214752 | ||||||
| chr1:220214836
|
C | T | 1 | a0001c0001t0002g0288 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.181-857G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214836 | ||||||
| chr1:220214843
|
T | C | 1 | a0001c0001t0030g0348 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.181-864A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214843 | ||||||
| chr1:220214921
|
CCTT | C | 31 | a0001c0001t0001g0047a0001c0001t0002g0030a0001c0001t0002g0031others(28): Show | 31 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.181-945_181-943del others(3): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214921 | ||||||
| chr1:220214945
|
A | AATATATA others(1): Show |
3 | a0001c0001t0004g0024a0002c0002t0007g0022a0002c0002t0007g0023 | 3 | HG00423.hp1 NA18954.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.181-967_181-966ins others(8): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214945 | ||||||
| chr1:220214945
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0026 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.181-967_181-966ins others(10): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214945 | ||||||
| chr1:220214945
|
A | AATATATA others(5): Show |
1 | a0002c0002t0008g0021 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.181-967_181-966ins others(12): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214945 | ||||||
| chr1:220214945
|
A | AATATATA others(9): Show |
1 | a0001c0001t0001g0025 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.181-967_181-966ins others(16): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214945 | ||||||
| chr1:220214945
|
A | T | 1 | a0001c0001t0018g0073 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.181-966T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214945 | ||||||
| chr1:220214946
|
T | A | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.181-967A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214946 | ||||||
| chr1:220214946
|
T | TATATATA others(6): Show |
1 | a0001c0001t0018g0073 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.181-968_181-967ins others(13): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214946 | ||||||
| chr1:220214946
|
T | TATATATA others(10): Show |
1 | a0001c0001t0004g0322 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.181-968_181-967ins others(17): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214946 | ||||||
| chr1:220214946
|
T | TATATATA others(12): Show |
1 | a0001c0001t0004g0227 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.181-968_181-967ins others(19): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214946 | ||||||
| chr1:220214946
|
T | TTA | 7 | a0001c0001t0001g0107a0001c0001t0001g0118a0001c0001t0001g0130others(4): Show | 7 | HG00735.hp2 HG01981.hp2 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.181-969_181-968dup others(2): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214946 | ||||||
| chr1:220214946
|
T | TTATA | 81 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(78): Show | 82 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.181-971_181-968dup others(4): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214946 | ||||||
| chr1:220214946
|
T | TTATATA | 24 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0090others(21): Show | 25 | HG00642.hp1 HG01071.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.181-973_181-968dup others(6): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214946 | ||||||
| chr1:220214946
|
T | TTATATAT others(1): Show |
18 | a0001c0001t0001g0062a0001c0001t0001g0098a0001c0001t0001g0116others(15): Show | 18 | HG00140.hp1 HG00408.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.181-975_181-968dup others(8): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214946 | ||||||
| chr1:220214946
|
T | TTATATAT others(3): Show |
23 | a0001c0001t0001g0076a0001c0001t0001g0079a0001c0001t0001g0086others(20): Show | 23 | HG00408.hp2 HG00544.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.181-977_181-968dup others(10): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214946 | ||||||
| chr1:220214946
|
T | TTATATAT others(5): Show |
24 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0083others(21): Show | 24 | HG00423.hp2 HG01891.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.181-979_181-968dup others(12): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214946 | ||||||
| chr1:220214946
|
T | TTATATAT others(7): Show |
28 | a0001c0001t0001g0074a0001c0001t0001g0084a0001c0001t0001g0085others(25): Show | 28 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.181-981_181-968dup others(14): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214946 | ||||||
| chr1:220214946
|
T | TTATATAT others(9): Show |
33 | a0001c0001t0001g0072a0001c0001t0001g0089a0001c0001t0001g0244others(30): Show | 34 | HG01358.hp1 HG01496.hp1 HG01975.hp2 others(31): Show |
intron_variant | MODIFIER | c.181-983_181-968dup others(16): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214946 | ||||||
| chr1:220214946
|
T | TTATATAT others(11): Show |
40 | a0001c0001t0002g0071a0001c0001t0002g0133a0001c0001t0002g0191others(37): Show | 40 | HG00140.hp2 HG00642.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.181-985_181-968dup others(18): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214946 | ||||||
| chr1:220214946
|
T | TTATATAT others(13): Show |
19 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0002g0289others(16): Show | 19 | HG00597.hp2 HG01952.hp2 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.181-987_181-968dup others(20): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214946 | ||||||
| chr1:220214946
|
T | TTATATAT others(15): Show |
2 | a0001c0001t0002g0291a0001c0001t0002g0318 | 2 | HG02300.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.181-989_181-968dup others(22): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214946 | ||||||
| chr1:220214946
|
T | TTATATAT others(17): Show |
1 | a0001c0001t0004g0323 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.181-991_181-968dup others(24): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214946 | ||||||
| chr1:220214946
|
T | TTATATAT others(19): Show |
1 | a0001c0001t0032g0268 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.181-993_181-968dup others(26): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214946 | ||||||
| chr1:220214946
|
T | TTATATGT others(11): Show |
1 | a0001c0001t0002g0350 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.181-968_181-967ins others(18): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214946 | ||||||
| chr1:220214946
|
TTATATAT others(1): Show |
T | 4 | a0003c0003t0006g0038a0003c0003t0006g0041a0003c0003t0006g0042others(1): Show | 4 | HG02004.hp2 HG02886.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.181-975_181-968del others(8): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214946 | ||||||
| chr1:220214946
|
TTATATAT others(3): Show |
T | 23 | a0001c0001t0001g0047a0001c0001t0002g0030a0001c0001t0002g0031others(20): Show | 23 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.181-977_181-968del others(10): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214946 | ||||||
| chr1:220214946
|
TTATATAT others(7): Show |
T | 5 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0272others(2): Show | 5 | HG02602.hp1 NA18948.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.181-981_181-968del others(14): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220214946 | ||||||
| chr1:220215113
|
G | A | 4 | a0001c0001t0003g0175a0001c0001t0003g0189a0001c0001t0003g0190others(1): Show | 4 | HG00544.hp1 HG00673.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.181-1134C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220215113 | ||||||
| chr1:220215120
|
G | A | 21 | a0001c0001t0001g0341a0001c0001t0002g0211a0001c0001t0002g0212others(18): Show | 22 | HG01261.hp2 HG01433.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.181-1141C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220215120 | ||||||
| chr1:220215509
|
A | T | 1 | a0001c0001t0004g0024 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.181-1530T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220215509 | ||||||
| chr1:220215521
|
A | T | 1 | a0001c0001t0004g0024 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.181-1542T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220215521 | ||||||
| chr1:220215545
|
G | T | 1 | a0001c0001t0004g0024 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.181-1566C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220215545 | ||||||
| chr1:220215546
|
T | G | 1 | a0001c0001t0004g0024 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.181-1567A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220215546 | ||||||
| chr1:220215604
|
G | A | 1 | a0001c0001t0022g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.181-1625C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220215604 | ||||||
| chr1:220215648
|
T | G | 21 | a0001c0001t0001g0025a0001c0001t0001g0026a0002c0002t0007g0002others(18): Show | 26 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.181-1669A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220215648 | ||||||
| chr1:220215726
|
T | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0157 | 2 | HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.181-1747A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220215726 | ||||||
| chr1:220215764
|
T | A | 6 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0213others(3): Show | 6 | HG01891.hp2 HG02630.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.181-1785A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220215764 | ||||||
| chr1:220216023
|
C | G | 2 | a0001c0001t0011g0351a0001c0001t0011g0352 | 2 | HG01243.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.181-2044G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220216023 | ||||||
| chr1:220216058
|
C | CA | 8 | a0001c0001t0002g0191a0001c0001t0002g0282a0001c0001t0002g0292others(5): Show | 8 | HG00544.hp2 HG02027.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.181-2080dupT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220216058 | ||||||
| chr1:220216120
|
G | A | 1 | a0001c0001t0029g0117 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.181-2141C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220216120 | ||||||
| chr1:220216129
|
T | A | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.181-2150A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220216129 | ||||||
| chr1:220216273
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.181-2294G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220216273 | ||||||
| chr1:220216496
|
C | T | 1 | a0001c0001t0004g0231 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.181-2517G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220216496 | ||||||
| chr1:220216521
|
A | T | 1 | a0001c0001t0004g0024 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.181-2542T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220216521 | ||||||
| chr1:220216561
|
T | A | 1 | a0001c0001t0001g0166 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.181-2582A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220216561 | ||||||
| chr1:220216593
|
G | A | 1 | a0001c0001t0004g0024 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.181-2614C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220216593 | ||||||
| chr1:220216594
|
A | G | 1 | a0001c0001t0004g0024 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.181-2615T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220216594 | ||||||
| chr1:220216622
|
T | A | 1 | a0001c0001t0004g0024 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.181-2643A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220216622 | ||||||
| chr1:220216702
|
C | G | 1 | a0001c0001t0002g0304 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.181-2723G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220216702 | ||||||
| chr1:220216784
|
T | C | 1 | a0001c0017t0001g0234 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.181-2805A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220216784 | ||||||
| chr1:220217273
|
A | C | 1 | a0001c0014t0001g0269 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.181-3294T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220217273 | ||||||
| chr1:220217558
|
A | G | 2 | a0001c0001t0003g0094a0001c0001t0004g0093 | 2 | NA18971.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.181-3579T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220217558 | ||||||
| chr1:220217580
|
C | T | 1 | a0001c0001t0002g0315 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.181-3601G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220217580 | ||||||
| chr1:220217637
|
A | G | 6 | a0001c0001t0002g0235a0001c0001t0002g0350a0001c0001t0017g0216others(3): Show | 6 | HG01891.hp1 HG02258.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.181-3658T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220217637 | ||||||
| chr1:220217664
|
T | C | 11 | a0001c0001t0003g0094a0001c0001t0004g0093a0001c0001t0005g0097others(8): Show | 11 | HG00609.hp1 NA18942.hp2 NA18953.hp1 others(8): Show |
intron_variant | MODIFIER | c.181-3685A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220217664 | ||||||
| chr1:220217775
|
T | C | 1 | a0001c0001t0005g0152 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.181-3796A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220217775 | ||||||
| chr1:220217810
|
T | G | 1 | a0003c0003t0006g0041 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.181-3831A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220217810 | ||||||
| chr1:220218176
|
C | T | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG01074.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.181-4197G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220218176 | ||||||
| chr1:220218213
|
C | T | 6 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(3): Show | 7 | HG00423.hp1 HG02027.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.181-4234G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220218213 | ||||||
| chr1:220218288
|
T | C | 1 | a0003c0003t0006g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.181-4309A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220218288 | ||||||
| chr1:220218334
|
A | T | 1 | a0001c0001t0001g0153 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.181-4355T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220218334 | ||||||
| chr1:220218339
|
A | G | 21 | a0001c0001t0001g0341a0001c0001t0002g0211a0001c0001t0002g0212others(18): Show | 22 | HG01261.hp2 HG01433.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.181-4360T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220218339 | ||||||
| chr1:220218392
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.181-4413C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220218392 | ||||||
| chr1:220218414
|
A | G | 1 | a0001c0001t0003g0200 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.181-4435T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220218414 | ||||||
| chr1:220218740
|
T | TA | 128 | a0001c0001t0001g0064a0001c0001t0001g0130a0001c0001t0001g0151others(125): Show | 128 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.181-4762dupT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220218740 | ||||||
| chr1:220218778
|
G | A | 1 | a0001c0001t0003g0193 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.181-4799C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220218778 | ||||||
| chr1:220218859
|
C | G | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.181-4880G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220218859 | ||||||
| chr1:220219070
|
A | C | 70 | a0001c0001t0001g0244a0001c0001t0002g0061a0001c0001t0002g0071others(67): Show | 70 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.181-5091T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220219070 | ||||||
| chr1:220219073
|
T | G | 1 | a0001c0001t0022g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.181-5094A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220219073 | ||||||
| chr1:220219216
|
G | C | 2 | a0001c0001t0002g0061a0001c0001t0002g0082 | 2 | HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.181-5237C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220219216 | ||||||
| chr1:220219251
|
CAT | C | 6 | a0001c0001t0001g0074a0001c0001t0001g0083a0001c0001t0001g0366others(3): Show | 6 | NA18944.hp2 NA18986.hp1 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.181-5274_181-5273d others(4): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220219251 | ||||||
| chr1:220219283
|
G | C | 1 | a0002c0002t0007g0004 | 2 | NA18993.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.181-5304C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220219283 | ||||||
| chr1:220219296
|
T | TA | 77 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(74): Show | 83 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.181-5318dupT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220219296 | ||||||
| chr1:220219483
|
T | C | 4 | a0001c0001t0002g0235a0001c0001t0002g0350a0001c0001t0022g0209others(1): Show | 4 | HG02258.hp2 HG02559.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.181-5504A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220219483 | ||||||
| chr1:220219559
|
T | C | 1 | a0001c0001t0003g0266 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.181-5580A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220219559 | ||||||
| chr1:220219633
|
C | T | 1 | a0001c0001t0003g0080 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.181-5654G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220219633 | ||||||
| chr1:220220017
|
T | C | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.181-6038A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220220017 | ||||||
| chr1:220220072
|
T | C | 28 | a0001c0001t0001g0047a0001c0001t0002g0030a0001c0001t0002g0031others(25): Show | 28 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.181-6093A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220220072 | ||||||
| chr1:220220172
|
C | G | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.181-6193G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220220172 | ||||||
| chr1:220220238
|
T | C | 10 | a0002c0002t0007g0002a0002c0002t0007g0009a0002c0002t0007g0010others(7): Show | 11 | HG00639.hp1 HG01074.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.181-6259A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220220238 | ||||||
| chr1:220220240
|
C | T | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG01074.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.181-6261G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220220240 | ||||||
| chr1:220220265
|
C | T | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.181-6286G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220220265 | ||||||
| chr1:220220274
|
C | T | 23 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0072others(20): Show | 23 | HG01358.hp2 HG01496.hp1 HG01934.hp2 others(20): Show |
intron_variant | MODIFIER | c.181-6295G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220220274 | ||||||
| chr1:220220298
|
T | A | 2 | a0001c0001t0017g0216a0001c0001t0017g0217 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.181-6319A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220220298 | ||||||
| chr1:220220389
|
A | T | 2 | a0002c0002t0007g0009a0002c0002t0007g0010 | 2 | HG01074.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.181-6410T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220220389 | ||||||
| chr1:220220522
|
T | C | 2 | a0003c0003t0006g0048a0003c0003t0006g0049 | 2 | HG00673.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.181-6543A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220220522 | ||||||
| chr1:220220559
|
A | G | 23 | a0001c0001t0001g0341a0001c0001t0002g0211a0001c0001t0002g0212others(20): Show | 24 | HG01261.hp2 HG01433.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.181-6580T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220220559 | ||||||
| chr1:220220804
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.181-6825A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220220804 | ||||||
| chr1:220220806
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.181-6827C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220220806 | ||||||
| chr1:220220818
|
A | G | 5 | a0001c0001t0002g0281a0001c0001t0002g0282a0001c0001t0002g0283others(2): Show | 5 | NA18747.hp1 NA18943.hp2 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.181-6839T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220220818 | ||||||
| chr1:220220848
|
G | A | 5 | a0001c0001t0002g0350a0001c0001t0013g0219a0001c0001t0013g0220others(2): Show | 5 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.181-6869C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220220848 | ||||||
| chr1:220220861
|
C | A | 1 | a0001c0001t0001g0244 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.181-6882G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220220861 | ||||||
| chr1:220221002
|
G | A | 23 | a0001c0001t0001g0047a0001c0001t0001g0134a0001c0001t0030g0348others(20): Show | 23 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.181-7023C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220221002 | ||||||
| chr1:220221298
|
A | G | 1 | a0001c0017t0001g0234 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.181-7319T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220221298 | ||||||
| chr1:220221667
|
G | A | 45 | a0001c0001t0001g0118a0001c0001t0001g0185a0001c0001t0002g0181others(42): Show | 47 | HG00544.hp1 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.181-7688C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220221667 | ||||||
| chr1:220221952
|
A | G | 1 | a0001c0001t0004g0225 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.181-7973T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220221952 | ||||||
| chr1:220222190
|
A | G | 1 | a0001c0001t0017g0216 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.181-8211T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220222190 | ||||||
| chr1:220222301
|
C | T | 6 | a0001c0001t0002g0235a0001c0001t0002g0350a0001c0001t0017g0216others(3): Show | 6 | HG01891.hp1 HG02258.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.181-8322G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220222301 | ||||||
| chr1:220222567
|
T | C | 2 | a0001c0001t0009g0343a0001c0001t0009g0344 | 2 | HG01884.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.181-8588A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220222567 | ||||||
| chr1:220222714
|
T | C | 1 | a0001c0001t0004g0036 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.181-8735A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220222714 | ||||||
| chr1:220222762
|
C | A | 1 | a0001c0001t0002g0350 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.181-8783G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220222762 | ||||||
| chr1:220222871
|
G | A | 2 | a0001c0001t0011g0351a0001c0001t0011g0352 | 2 | HG01243.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.181-8892C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220222871 | ||||||
| chr1:220222874
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0002g0060 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.181-8895C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220222874 | ||||||
| chr1:220222939
|
G | A | 369 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(366): Show | 377 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(374): Show |
intron_variant | MODIFIER | c.181-8960C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220222939 | ||||||
| chr1:220223040
|
T | G | 2 | a0001c0001t0011g0351a0001c0001t0011g0352 | 2 | HG01243.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.181-9061A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220223040 | ||||||
| chr1:220223181
|
G | A | 1 | a0001c0001t0028g0264 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.181-9202C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220223181 | ||||||
| chr1:220223268
|
T | C | 1 | a0003c0003t0006g0049 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.181-9289A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220223268 | ||||||
| chr1:220223326
|
T | C | 1 | a0001c0001t0002g0292 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.181-9347A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220223326 | ||||||
| chr1:220223381
|
T | G | 1 | a0001c0001t0003g0194 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.181-9402A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220223381 | ||||||
| chr1:220223430
|
T | C | 23 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0002g0302others(20): Show | 28 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.180+9369A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220223430 | ||||||
| chr1:220223438
|
G | A | 1 | a0001c0001t0026g0224 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.180+9361C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220223438 | ||||||
| chr1:220223574
|
A | G | 39 | a0001c0001t0001g0047a0001c0001t0002g0030a0001c0001t0002g0031others(36): Show | 39 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.180+9225T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220223574 | ||||||
| chr1:220223599
|
C | G | 3 | a0001c0004t0002g0345a0001c0004t0009g0338a0001c0004t0009g0342 | 3 | HG01433.hp1 HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.180+9200G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220223599 | ||||||
| chr1:220223655
|
A | G | 1 | a0001c0001t0003g0266 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.180+9144T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220223655 | ||||||
| chr1:220223694
|
T | TA | 22 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0074others(19): Show | 22 | HG01358.hp2 HG01496.hp1 HG01934.hp2 others(19): Show |
intron_variant | MODIFIER | c.180+9104dupT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220223694 | ||||||
| chr1:220223694
|
TA | T | 23 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0002g0315others(20): Show | 28 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.180+9104delT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220223694 | ||||||
| chr1:220223939
|
G | A | 3 | a0001c0001t0002g0235a0001c0001t0002g0350a0001c0001t0026g0224 | 3 | HG02258.hp2 HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.180+8860C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220223939 | ||||||
| chr1:220224005
|
C | CA | 51 | a0001c0001t0001g0101a0001c0001t0001g0145a0001c0001t0001g0149others(48): Show | 53 | HG00544.hp1 HG00558.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.180+8793dupT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220224005 | ||||||
| chr1:220224005
|
C | CAA | 35 | a0001c0001t0001g0047a0001c0001t0002g0030a0001c0001t0002g0032others(32): Show | 35 | HG00621.hp1 HG00673.hp1 HG01361.hp1 others(32): Show |
intron_variant | MODIFIER | c.180+8792_180+8793d others(4): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220224005 | ||||||
| chr1:220224005
|
CA | C | 181 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0059others(178): Show | 186 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.180+8793delT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220224005 | ||||||
| chr1:220224005
|
CAA | C | 9 | a0001c0001t0001g0244a0001c0001t0002g0271a0001c0001t0002g0293others(6): Show | 9 | HG00639.hp1 HG01069.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.180+8792_180+8793d others(4): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220224005 | ||||||
| chr1:220224056
|
A | C | 1 | a0001c0001t0002g0298 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.180+8743T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220224056 | ||||||
| chr1:220224094
|
C | T | 4 | a0001c0001t0002g0235a0001c0001t0002g0350a0001c0001t0022g0209others(1): Show | 4 | HG02258.hp2 HG02559.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.180+8705G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220224094 | ||||||
| chr1:220224459
|
T | C | 11 | a0001c0001t0001g0069a0001c0001t0001g0077a0001c0001t0001g0078others(8): Show | 11 | HG01358.hp2 HG01496.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.180+8340A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220224459 | ||||||
| chr1:220224739
|
A | T | 2 | a0001c0001t0004g0034a0001c0001t0004g0035 | 2 | HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.180+8060T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220224739 | ||||||
| chr1:220224894
|
G | T | 1 | a0001c0001t0001g0066 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.180+7905C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220224894 | ||||||
| chr1:220225015
|
A | G | 3 | a0001c0001t0004g0237a0001c0001t0004g0238a0001c0001t0004g0239 | 3 | HG02723.hp1 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.180+7784T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220225015 | ||||||
| chr1:220225070
|
C | T | 2 | a0001c0001t0009g0343a0001c0001t0009g0344 | 2 | HG01884.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.180+7729G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220225070 | ||||||
| chr1:220225078
|
T | C | 1 | a0001c0014t0001g0269 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.180+7721A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220225078 | ||||||
| chr1:220226100
|
A | G | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.180+6699T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220226100 | ||||||
| chr1:220226227
|
C | T | 6 | a0001c0001t0011g0351a0001c0001t0011g0352a0001c0001t0013g0219others(3): Show | 6 | HG01243.hp2 HG02055.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.180+6572G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220226227 | ||||||
| chr1:220226240
|
G | T | 2 | a0003c0003t0006g0048a0003c0003t0006g0049 | 2 | HG00673.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.180+6559C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220226240 | ||||||
| chr1:220226325
|
C | T | 2 | a0001c0001t0017g0216a0001c0001t0017g0217 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.180+6474G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220226325 | ||||||
| chr1:220226432
|
T | TA | 21 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(18): Show | 26 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.180+6366dupT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220226432 | ||||||
| chr1:220226493
|
G | T | 2 | a0001c0001t0001g0244a0001c0004t0009g0223 | 2 | HG02055.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.180+6306C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220226493 | ||||||
| chr1:220226566
|
T | G | 56 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0247others(53): Show | 56 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.180+6233A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220226566 | ||||||
| chr1:220226665
|
T | C | 1 | a0001c0001t0005g0152 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.180+6134A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220226665 | ||||||
| chr1:220226722
|
G | GCCCAATT others(44): Show |
1 | a0001c0001t0003g0171 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.180+6026_180+6076d others(53): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220226722 | ||||||
| chr1:220226878
|
T | C | 1 | a0001c0001t0032g0268 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.180+5921A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220226878 | ||||||
| chr1:220227072
|
G | A | 1 | a0001c0001t0003g0171 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.180+5727C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220227072 | ||||||
| chr1:220227229
|
A | T | 1 | a0001c0001t0001g0159 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.180+5570T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220227229 | ||||||
| chr1:220227258
|
C | T | 14 | a0001c0001t0001g0047a0003c0003t0002g0053a0003c0003t0002g0054others(11): Show | 14 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.180+5541G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220227258 | ||||||
| chr1:220227269
|
G | A | 2 | a0001c0001t0015g0339a0001c0001t0015g0340 | 2 | HG01261.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.180+5530C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220227269 | ||||||
| chr1:220227470
|
A | C | 1 | a0001c0001t0001g0109 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.180+5329T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220227470 | ||||||
| chr1:220227651
|
C | T | 1 | a0001c0001t0003g0243 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.180+5148G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220227651 | ||||||
| chr1:220227657
|
A | G | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.180+5142T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220227657 | ||||||
| chr1:220227667
|
T | C | 212 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(209): Show | 218 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.180+5132A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220227667 | ||||||
| chr1:220227789
|
T | C | 1 | a0001c0001t0002g0283 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.180+5010A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220227789 | ||||||
| chr1:220227821
|
G | A | 1 | a0001c0001t0002g0133 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.180+4978C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220227821 | ||||||
| chr1:220227823
|
C | T | 1 | a0001c0001t0013g0221 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.180+4976G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220227823 | ||||||
| chr1:220227828
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.180+4971A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220227828 | ||||||
| chr1:220227842
|
C | T | 9 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0032others(6): Show | 9 | HG01884.hp1 HG02145.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.180+4957G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220227842 | ||||||
| chr1:220227978
|
C | G | 12 | a0001c0001t0001g0341a0001c0001t0009g0343a0001c0001t0009g0344others(9): Show | 13 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.180+4821G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220227978 | ||||||
| chr1:220227998
|
C | T | 44 | a0001c0001t0001g0185a0001c0001t0002g0181a0001c0001t0002g0191others(41): Show | 46 | HG00544.hp1 HG00558.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.180+4801G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220227998 | ||||||
| chr1:220228033
|
G | A | 5 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0272others(2): Show | 5 | HG02602.hp1 NA18948.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.180+4766C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220228033 | ||||||
| chr1:220228043
|
G | A | 2 | a0001c0001t0002g0235a0001c0001t0026g0224 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.180+4756C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220228043 | ||||||
| chr1:220228092
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.180+4707C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220228092 | ||||||
| chr1:220228135
|
C | T | 4 | a0001c0001t0013g0219a0001c0001t0013g0220a0001c0001t0013g0221others(1): Show | 4 | HG02055.hp2 HG02723.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.180+4664G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220228135 | ||||||
| chr1:220228376
|
T | C | 3 | a0001c0001t0001g0072a0001c0001t0001g0353a0002c0002t0008g0354 | 3 | HG03688.hp2 HG03710.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.180+4423A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220228376 | ||||||
| chr1:220228454
|
T | C | 1 | a0001c0001t0002g0350 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.180+4345A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220228454 | ||||||
| chr1:220228826
|
G | A | 40 | a0001c0001t0001g0047a0001c0001t0002g0030a0001c0001t0002g0031others(37): Show | 40 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.180+3973C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220228826 | ||||||
| chr1:220228897
|
G | A | 2 | a0001c0001t0011g0351a0001c0001t0011g0352 | 2 | HG01243.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.180+3902C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220228897 | ||||||
| chr1:220228989
|
T | G | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.180+3810A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220228989 | ||||||
| chr1:220229061
|
T | C | 189 | a0001c0001t0001g0047a0001c0001t0001g0059a0001c0001t0001g0064others(186): Show | 190 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.180+3738A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220229061 | ||||||
| chr1:220229246
|
A | G | 1 | a0001c0001t0014g0246 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.180+3553T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220229246 | ||||||
| chr1:220229307
|
T | C | 1 | a0001c0001t0002g0317 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.180+3492A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220229307 | ||||||
| chr1:220229333
|
T | C | 1 | a0001c0001t0003g0197 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.180+3466A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220229333 | ||||||
| chr1:220229400
|
C | A | 11 | a0001c0001t0003g0094a0001c0001t0004g0093a0001c0001t0005g0097others(8): Show | 11 | HG00609.hp1 NA18942.hp2 NA18953.hp1 others(8): Show |
intron_variant | MODIFIER | c.180+3399G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220229400 | ||||||
| chr1:220229517
|
T | C | 1 | a0001c0001t0027g0027 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.180+3282A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220229517 | ||||||
| chr1:220229571
|
T | C | 7 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0032others(4): Show | 7 | HG02145.hp2 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.180+3228A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220229571 | ||||||
| chr1:220229711
|
A | G | 1 | a0001c0001t0014g0246 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.180+3088T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220229711 | ||||||
| chr1:220229722
|
A | G | 1 | a0001c0001t0005g0110 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.180+3077T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220229722 | ||||||
| chr1:220229828
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | NA18981.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.180+2971C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220229828 | ||||||
| chr1:220229891
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.180+2908T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220229891 | ||||||
| chr1:220229909
|
C | T | 15 | a0001c0001t0001g0341a0001c0001t0009g0343a0001c0001t0009g0344others(12): Show | 16 | HG01261.hp2 HG01433.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.180+2890G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220229909 | ||||||
| chr1:220229977
|
A | G | 1 | a0001c0001t0002g0213 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.180+2822T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220229977 | ||||||
| chr1:220230329
|
A | G | 16 | a0001c0001t0001g0341a0001c0001t0002g0350a0001c0001t0009g0343others(13): Show | 17 | HG01261.hp2 HG01433.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.180+2470T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220230329 | ||||||
| chr1:220230345
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.180+2454G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220230345 | ||||||
| chr1:220230449
|
G | A | 1 | a0001c0014t0001g0269 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.180+2350C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220230449 | ||||||
| chr1:220230549
|
G | A | 2 | a0001c0001t0017g0216a0001c0001t0017g0217 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.180+2250C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220230549 | ||||||
| chr1:220230829
|
C | T | 3 | a0002c0002t0007g0004a0002c0002t0007g0022a0002c0002t0007g0023 | 4 | HG00423.hp1 NA18954.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.180+1970G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220230829 | ||||||
| chr1:220230962
|
C | T | 1 | a0001c0001t0002g0303 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.180+1837G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220230962 | ||||||
| chr1:220231038
|
T | G | 3 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068 | 3 | HG00597.hp1 HG00621.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.180+1761A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220231038 | ||||||
| chr1:220231062
|
T | C | 2 | a0001c0001t0017g0216a0001c0001t0017g0217 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.180+1737A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220231062 | ||||||
| chr1:220231369
|
A | G | 212 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(209): Show | 218 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.180+1430T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220231369 | ||||||
| chr1:220231494
|
T | C | 1 | a0001c0001t0004g0227 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.180+1305A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220231494 | ||||||
| chr1:220231501
|
A | G | 10 | a0001c0001t0001g0337a0001c0001t0004g0323a0001c0001t0004g0324others(7): Show | 10 | HG01346.hp2 HG01975.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.180+1298T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220231501 | ||||||
| chr1:220231528
|
T | TA | 46 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0337others(43): Show | 46 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.180+1270dupT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220231528 | ||||||
| chr1:220231570
|
G | A | 1 | a0001c0001t0030g0348 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.180+1229C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220231570 | ||||||
| chr1:220231570
|
G | T | 1 | a0001c0001t0001g0087 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.180+1229C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220231570 | ||||||
| chr1:220231615
|
C | G | 1 | a0001c0001t0001g0068 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.180+1184G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220231615 | ||||||
| chr1:220231711
|
C | A | 9 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0032others(6): Show | 9 | HG01884.hp1 HG02145.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.180+1088G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220231711 | ||||||
| chr1:220231745
|
G | C | 2 | a0001c0001t0004g0238a0001c0001t0004g0239 | 2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.180+1054C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220231745 | ||||||
| chr1:220231751
|
C | T | 123 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0228others(120): Show | 123 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.180+1048G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220231751 | ||||||
| chr1:220231775
|
A | G | 1 | a0001c0001t0002g0297 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.180+1024T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220231775 | ||||||
| chr1:220231938
|
G | A | 1 | a0001c0001t0002g0301 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.180+861C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220231938 | ||||||
| chr1:220231975
|
G | A | 1 | a0001c0001t0005g0250 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.180+824C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220231975 | ||||||
| chr1:220232120
|
G | A | 4 | a0001c0001t0013g0219a0001c0001t0013g0220a0001c0001t0013g0221others(1): Show | 4 | HG02055.hp2 HG02723.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.180+679C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220232120 | ||||||
| chr1:220232337
|
A | C | 1 | a0001c0001t0004g0324 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.180+462T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220232337 | ||||||
| chr1:220232367
|
T | C | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.180+432A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220232367 | ||||||
| chr1:220232461
|
C | T | 1 | a0001c0001t0010g0102 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.180+338G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220232461 | ||||||
| chr1:220232497
|
C | T | 1 | a0001c0001t0028g0264 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.180+302G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220232497 | ||||||
| chr1:220232712
|
T | C | 30 | a0001c0001t0001g0047a0001c0001t0002g0211a0001c0001t0002g0212others(27): Show | 30 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.180+87A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 2/34 | chr1 | 220232712 | ||||||
| chr1:220232949
|
A | G | 212 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(209): Show | 218 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.116-86T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220232949 | ||||||
| chr1:220233236
|
C | T | 1 | a0001c0001t0004g0024 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.116-373G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220233236 | ||||||
| chr1:220233242
|
T | TA | 10 | a0001c0001t0001g0151a0001c0001t0002g0030a0001c0001t0002g0031others(7): Show | 10 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.116-380dupT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220233242 | ||||||
| chr1:220233242
|
TA | T | 6 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0213others(3): Show | 6 | HG01891.hp2 HG02630.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-380delT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220233242 | ||||||
| chr1:220233423
|
G | A | 1 | a0001c0001t0011g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.116-560C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220233423 | ||||||
| chr1:220233511
|
A | T | 1 | a0001c0001t0001g0072 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.116-648T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220233511 | ||||||
| chr1:220233513
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.116-650T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220233513 | ||||||
| chr1:220233573
|
C | CA | 5 | a0001c0001t0003g0263a0001c0001t0003g0265a0001c0001t0012g0267others(2): Show | 5 | HG01243.hp1 HG03486.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.116-711dupT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220233573 | ||||||
| chr1:220233636
|
G | A | 1 | a0012c0006t0003g0008 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.116-773C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220233636 | ||||||
| chr1:220233794
|
G | A | 16 | a0002c0002t0007g0002a0002c0002t0007g0009a0002c0002t0007g0010others(13): Show | 20 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.116-931C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220233794 | ||||||
| chr1:220233967
|
T | C | 2 | a0002c0002t0008g0020a0002c0002t0008g0021 | 2 | HG03927.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.116-1104A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220233967 | ||||||
| chr1:220234013
|
A | G | 212 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(209): Show | 218 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.116-1150T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220234013 | ||||||
| chr1:220234016
|
T | A | 8 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0004g0034others(5): Show | 8 | HG02886.hp2 HG02922.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.116-1153A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220234016 | ||||||
| chr1:220234147
|
G | A | 2 | a0001c0001t0001g0151a0001c0001t0001g0153 | 2 | HG01109.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.116-1284C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220234147 | ||||||
| chr1:220234205
|
C | A | 1 | a0001c0001t0002g0212 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.116-1342G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220234205 | ||||||
| chr1:220234245
|
T | C | 123 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0228others(120): Show | 123 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.116-1382A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220234245 | ||||||
| chr1:220234284
|
A | T | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.116-1421T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220234284 | ||||||
| chr1:220234288
|
T | C | 3 | a0001c0001t0002g0235a0001c0001t0022g0209a0001c0001t0026g0224 | 3 | HG02559.hp2 HG03471.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.116-1425A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220234288 | ||||||
| chr1:220234297
|
T | TGGGACTG others(80): Show |
6 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(3): Show | 7 | HG00423.hp1 HG02027.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.116-1521_116-1435d others(89): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220234297 | ||||||
| chr1:220234331
|
AATAGATT others(7): Show |
A | 1 | a0001c0001t0001g0067 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.116-1482_116-1469d others(16): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220234331 | ||||||
| chr1:220234350
|
G | A | 2 | a0001c0001t0009g0346a0001c0001t0009g0347 | 2 | HG02109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.116-1487C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220234350 | ||||||
| chr1:220234544
|
A | G | 9 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0032others(6): Show | 9 | HG01884.hp1 HG02145.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.116-1681T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220234544 | ||||||
| chr1:220234549
|
T | C | 9 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0032others(6): Show | 9 | HG01884.hp1 HG02145.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.116-1686A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220234549 | ||||||
| chr1:220234708
|
A | G | 1 | a0001c0001t0002g0357 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.116-1845T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220234708 | ||||||
| chr1:220234718
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.116-1855C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220234718 | ||||||
| chr1:220234763
|
G | C | 1 | a0001c0001t0028g0264 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.116-1900C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220234763 | ||||||
| chr1:220235059
|
A | G | 2 | a0001c0001t0011g0351a0001c0001t0011g0352 | 2 | HG01243.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.116-2196T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220235059 | ||||||
| chr1:220235333
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.116-2470A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220235333 | ||||||
| chr1:220235497
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.116-2634A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220235497 | ||||||
| chr1:220235549
|
A | G | 1 | a0001c0001t0003g0168 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.116-2686T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220235549 | ||||||
| chr1:220235570
|
T | C | 5 | a0001c0001t0010g0102a0001c0001t0010g0103a0001c0001t0010g0105others(2): Show | 5 | HG01258.hp1 HG01934.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-2707A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220235570 | ||||||
| chr1:220235684
|
G | T | 1 | a0001c0001t0005g0152 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.116-2821C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220235684 | ||||||
| chr1:220235755
|
T | C | 1 | a0001c0001t0016g0173 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.116-2892A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220235755 | ||||||
| chr1:220235785
|
C | A | 1 | a0001c0001t0005g0152 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.116-2922G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220235785 | ||||||
| chr1:220235885
|
G | C | 1 | a0001c0001t0001g0101 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.116-3022C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220235885 | ||||||
| chr1:220235904
|
C | A | 6 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0213others(3): Show | 6 | HG01891.hp2 HG02630.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-3041G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220235904 | ||||||
| chr1:220235934
|
G | C | 2 | a0001c0001t0017g0216a0001c0001t0017g0217 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.116-3071C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220235934 | ||||||
| chr1:220235966
|
T | C | 17 | a0001c0001t0001g0341a0001c0001t0002g0350a0001c0001t0009g0343others(14): Show | 18 | HG01261.hp2 HG01433.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.116-3103A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220235966 | ||||||
| chr1:220236039
|
A | C | 1 | a0001c0001t0002g0350 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.116-3176T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220236039 | ||||||
| chr1:220236166
|
ATTTATT | A | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.116-3309_116-3304d others(8): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220236166 | ||||||
| chr1:220236301
|
C | T | 2 | a0001c0001t0004g0229a0001c0001t0004g0230 | 2 | NA18612.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.116-3438G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220236301 | ||||||
| chr1:220236385
|
C | T | 1 | a0002c0007t0008g0018 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.116-3522G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220236385 | ||||||
| chr1:220236444
|
G | A | 1 | a0001c0001t0017g0217 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.116-3581C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220236444 | ||||||
| chr1:220236469
|
C | T | 1 | a0001c0001t0004g0226 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.116-3606G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220236469 | ||||||
| chr1:220236502
|
A | G | 3 | a0001c0001t0002g0235a0001c0001t0022g0209a0001c0001t0026g0224 | 3 | HG02559.hp2 HG03471.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.116-3639T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220236502 | ||||||
| chr1:220236510
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.116-3647T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220236510 | ||||||
| chr1:220236641
|
C | T | 2 | a0001c0001t0004g0324a0001c0001t0004g0325 | 2 | NA18986.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.116-3778G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220236641 | ||||||
| chr1:220236864
|
A | C | 123 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0228others(120): Show | 123 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.116-4001T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220236864 | ||||||
| chr1:220236929
|
C | G | 17 | a0001c0001t0001g0341a0001c0001t0002g0350a0001c0001t0009g0343others(14): Show | 18 | HG01261.hp2 HG01433.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.116-4066G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220236929 | ||||||
| chr1:220237049
|
T | C | 2 | a0001c0001t0017g0216a0001c0001t0017g0217 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.116-4186A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220237049 | ||||||
| chr1:220237104
|
A | T | 54 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0247others(51): Show | 54 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.116-4241T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220237104 | ||||||
| chr1:220237139
|
A | G | 8 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0004g0034others(5): Show | 8 | HG02886.hp2 HG02922.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.116-4276T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220237139 | ||||||
| chr1:220237473
|
G | A | 39 | a0001c0001t0001g0047a0001c0001t0002g0030a0001c0001t0002g0031others(36): Show | 39 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.116-4610C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220237473 | ||||||
| chr1:220237516
|
A | G | 1 | a0001c0001t0017g0216 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.116-4653T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220237516 | ||||||
| chr1:220237554
|
G | A | 6 | a0002c0002t0008g0001a0002c0002t0008g0003a0002c0002t0008g0019others(3): Show | 9 | HG00558.hp1 HG03927.hp1 HG04184.hp1 others(6): Show |
intron_variant | MODIFIER | c.116-4691C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220237554 | ||||||
| chr1:220237676
|
A | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0157 | 2 | HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.116-4813T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220237676 | ||||||
| chr1:220237728
|
A | C | 9 | a0001c0001t0001g0059a0001c0001t0002g0060a0001c0001t0002g0061others(6): Show | 9 | HG01243.hp1 HG02717.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.116-4865T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220237728 | ||||||
| chr1:220237799
|
T | C | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.116-4936A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220237799 | ||||||
| chr1:220237884
|
T | TA | 9 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(6): Show | 9 | HG00558.hp1 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.116-5022dupT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220237884 | ||||||
| chr1:220237884
|
TAA | T | 37 | a0001c0001t0001g0047a0001c0001t0002g0030a0001c0001t0002g0031others(34): Show | 37 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.116-5023_116-5022d others(4): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220237884 | ||||||
| chr1:220238087
|
T | C | 1 | a0001c0001t0024g0222 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.116-5224A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220238087 | ||||||
| chr1:220238449
|
T | C | 1 | a0001c0001t0014g0246 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.116-5586A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220238449 | ||||||
| chr1:220238628
|
A | G | 40 | a0001c0001t0001g0047a0001c0001t0002g0030a0001c0001t0002g0031others(37): Show | 40 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.116-5765T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220238628 | ||||||
| chr1:220239224
|
C | G | 2 | a0002c0002t0008g0020a0002c0002t0008g0021 | 2 | HG03927.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.116-6361G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220239224 | ||||||
| chr1:220239266
|
T | C | 2 | a0002c0002t0008g0020a0002c0002t0008g0021 | 2 | HG03927.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.116-6403A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220239266 | ||||||
| chr1:220239387
|
T | C | 1 | a0001c0001t0031g0257 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.116-6524A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220239387 | ||||||
| chr1:220239544
|
T | A | 2 | a0001c0001t0002g0235a0001c0001t0026g0224 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.116-6681A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220239544 | ||||||
| chr1:220239567
|
T | C | 1 | a0001c0001t0014g0246 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.116-6704A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220239567 | ||||||
| chr1:220239609
|
A | T | 1 | a0001c0004t0009g0342 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.116-6746T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220239609 | ||||||
| chr1:220239792
|
C | T | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.116-6929G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220239792 | ||||||
| chr1:220239989
|
TA | T | 174 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0064others(171): Show | 180 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.116-7127delT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220239989 | ||||||
| chr1:220239989
|
TAA | T | 7 | a0001c0001t0001g0059a0001c0001t0002g0061a0001c0001t0002g0302others(4): Show | 7 | HG01891.hp1 HG01975.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.116-7128_116-7127d others(4): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220239989 | ||||||
| chr1:220240140
|
T | C | 1 | a0002c0002t0008g0019 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.116-7277A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220240140 | ||||||
| chr1:220240215
|
T | C | 40 | a0001c0001t0001g0047a0001c0001t0002g0030a0001c0001t0002g0031others(37): Show | 40 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.116-7352A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220240215 | ||||||
| chr1:220240496
|
C | T | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.116-7633G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220240496 | ||||||
| chr1:220240927
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0228 | 2 | NA18955.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.116-8064G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220240927 | ||||||
| chr1:220241530
|
A | G | 212 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(209): Show | 218 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.116-8667T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220241530 | ||||||
| chr1:220241811
|
T | C | 6 | a0001c0001t0003g0241a0001c0001t0004g0240a0001c0001t0004g0251others(3): Show | 6 | HG02015.hp1 HG02135.hp2 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.116-8948A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220241811 | ||||||
| chr1:220241831
|
C | T | 212 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(209): Show | 218 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.116-8968G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220241831 | ||||||
| chr1:220241872
|
T | C | 9 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0004g0034others(6): Show | 9 | HG02004.hp2 HG02886.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.116-9009A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220241872 | ||||||
| chr1:220242402
|
T | A | 1 | a0001c0001t0009g0347 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.116-9539A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220242402 | ||||||
| chr1:220242408
|
A | T | 2 | a0001c0001t0001g0059a0001c0001t0002g0060 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.116-9545T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220242408 | ||||||
| chr1:220242425
|
C | T | 2 | a0001c0001t0011g0351a0001c0001t0011g0352 | 2 | HG01243.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.116-9562G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220242425 | ||||||
| chr1:220242517
|
T | TA | 212 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(209): Show | 218 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.116-9655_116-9654i others(3): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220242517 | ||||||
| chr1:220242587
|
T | TGGTATAA others(3): Show |
43 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0337others(40): Show | 43 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.116-9725_116-9724i others(12): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220242587 | ||||||
| chr1:220242649
|
C | T | 1 | a0001c0001t0017g0216 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.116-9786G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220242649 | ||||||
| chr1:220242650
|
A | G | 1 | a0001c0001t0014g0246 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.116-9787T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220242650 | ||||||
| chr1:220242670
|
T | C | 6 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0213others(3): Show | 6 | HG01891.hp2 HG02630.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-9807A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220242670 | ||||||
| chr1:220242726
|
G | A | 6 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0213others(3): Show | 6 | HG01891.hp2 HG02630.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-9863C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220242726 | ||||||
| chr1:220242857
|
G | A | 2 | a0001c0001t0022g0209a0001c0001t0026g0224 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.116-9994C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220242857 | ||||||
| chr1:220242860
|
C | T | 1 | a0001c0001t0030g0348 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.116-9997G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220242860 | ||||||
| chr1:220243055
|
T | A | 1 | a0010c0018t0003g0207 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.116-10192A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220243055 | ||||||
| chr1:220243085
|
C | T | 235 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(232): Show | 241 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(238): Show |
intron_variant | MODIFIER | c.116-10222G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220243085 | ||||||
| chr1:220243121
|
G | A | 1 | a0001c0004t0009g0342 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.116-10258C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220243121 | ||||||
| chr1:220243163
|
G | A | 1 | a0001c0001t0017g0217 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.116-10300C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220243163 | ||||||
| chr1:220243189
|
C | A | 1 | a0001c0001t0002g0040 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.116-10326G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220243189 | ||||||
| chr1:220243211
|
G | A | 1 | a0001c0001t0024g0222 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.116-10348C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220243211 | ||||||
| chr1:220243241
|
C | A | 1 | a0002c0002t0008g0021 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.116-10378G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220243241 | ||||||
| chr1:220243353
|
C | CA | 14 | a0001c0001t0001g0062a0001c0001t0001g0121a0001c0001t0001g0122others(11): Show | 14 | HG01258.hp1 HG01934.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.116-10491dupT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220243353 | ||||||
| chr1:220243353
|
CA | C | 205 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(202): Show | 211 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.116-10491delT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220243353 | ||||||
| chr1:220243353
|
CAA | C | 8 | a0001c0001t0001g0341a0001c0001t0002g0211a0001c0001t0002g0212others(5): Show | 8 | HG00558.hp1 HG01891.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.116-10492_116-1049 others(6): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220243353 | ||||||
| chr1:220243395
|
C | T | 39 | a0001c0001t0001g0047a0001c0001t0002g0030a0001c0001t0002g0031others(36): Show | 39 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.116-10532G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220243395 | ||||||
| chr1:220243530
|
T | C | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.116-10667A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220243530 | ||||||
| chr1:220243727
|
A | G | 1 | a0001c0001t0002g0296 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.116-10864T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220243727 | ||||||
| chr1:220243791
|
C | G | 123 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0228others(120): Show | 123 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.116-10928G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220243791 | ||||||
| chr1:220243812
|
T | G | 1 | a0001c0001t0017g0216 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.116-10949A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220243812 | ||||||
| chr1:220244131
|
C | T | 1 | a0001c0001t0006g0108 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.116-11268G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220244131 | ||||||
| chr1:220244248
|
A | G | 364 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(361): Show | 372 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(369): Show |
intron_variant | MODIFIER | c.116-11385T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220244248 | ||||||
| chr1:220244367
|
C | T | 39 | a0001c0001t0001g0047a0001c0001t0002g0030a0001c0001t0002g0031others(36): Show | 39 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.116-11504G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220244367 | ||||||
| chr1:220244569
|
T | C | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.116-11706A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220244569 | ||||||
| chr1:220244588
|
G | A | 1 | a0001c0001t0003g0265 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.116-11725C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220244588 | ||||||
| chr1:220244879
|
T | C | 1 | a0002c0002t0007g0023 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.116-12016A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220244879 | ||||||
| chr1:220245124
|
G | GA | 84 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(81): Show | 90 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.116-12262dupT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220245124 | ||||||
| chr1:220245192
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.116-12329C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220245192 | ||||||
| chr1:220245204
|
C | T | 18 | a0001c0001t0001g0341a0001c0001t0002g0350a0001c0001t0009g0343others(15): Show | 19 | HG00735.hp1 HG01261.hp2 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.116-12341G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220245204 | ||||||
| chr1:220245258
|
G | A | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.116-12395C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220245258 | ||||||
| chr1:220245281
|
C | A | 2 | a0001c0001t0001g0059a0001c0001t0002g0060 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.116-12418G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220245281 | ||||||
| chr1:220245292
|
C | T | 17 | a0001c0001t0001g0341a0001c0001t0002g0350a0001c0001t0009g0343others(14): Show | 18 | HG01261.hp2 HG01433.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.116-12429G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220245292 | ||||||
| chr1:220245309
|
G | A | 51 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0247others(48): Show | 51 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.116-12446C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220245309 | ||||||
| chr1:220245310
|
C | T | 3 | a0001c0001t0011g0351a0001c0001t0011g0352a0001c0001t0024g0222 | 3 | HG01243.hp2 HG02055.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.116-12447G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220245310 | ||||||
| chr1:220245315
|
C | T | 51 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0247others(48): Show | 51 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.116-12452G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220245315 | ||||||
| chr1:220245316
|
A | G | 51 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0247others(48): Show | 51 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.116-12453T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220245316 | ||||||
| chr1:220245327
|
G | A | 3 | a0001c0001t0002g0312a0001c0001t0002g0313a0001c0001t0012g0314 | 3 | HG01952.hp2 NA18966.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.116-12464C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220245327 | ||||||
| chr1:220245345
|
G | C | 3 | a0002c0002t0007g0004a0002c0002t0007g0022a0002c0002t0007g0023 | 4 | HG00423.hp1 NA18954.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-12482C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220245345 | ||||||
| chr1:220245360
|
C | T | 4 | a0001c0001t0002g0275a0001c0001t0002g0276a0001c0001t0003g0358others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-12497G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220245360 | ||||||
| chr1:220245394
|
A | G | 13 | a0001c0001t0001g0341a0001c0001t0009g0343a0001c0001t0009g0344others(10): Show | 14 | HG01433.hp1 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.116-12531T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220245394 | ||||||
| chr1:220245400
|
T | G | 1 | a0001c0001t0001g0085 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.116-12537A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220245400 | ||||||
| chr1:220245409
|
A | G | 1 | a0001c0001t0003g0243 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.116-12546T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220245409 | ||||||
| chr1:220245410
|
A | C | 124 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0085others(121): Show | 124 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.116-12547T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220245410 | ||||||
| chr1:220245517
|
A | G | 1 | a0001c0001t0004g0322 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.116-12654T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220245517 | ||||||
| chr1:220245519
|
G | A | 1 | a0001c0001t0001g0366 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.116-12656C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220245519 | ||||||
| chr1:220245532
|
C | T | 2 | a0001c0001t0017g0216a0001c0001t0017g0217 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.116-12669G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220245532 | ||||||
| chr1:220245551
|
A | G | 7 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0032others(4): Show | 7 | HG02145.hp2 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.116-12688T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220245551 | ||||||
| chr1:220245637
|
C | G | 16 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0003g0241others(13): Show | 16 | HG00423.hp2 HG00597.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.116-12774G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220245637 | ||||||
| chr1:220245645
|
C | T | 211 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(208): Show | 217 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.116-12782G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220245645 | ||||||
| chr1:220245647
|
C | G | 211 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(208): Show | 217 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.116-12784G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220245647 | ||||||
| chr1:220245743
|
A | C | 1 | a0001c0001t0002g0212 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.116-12880T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220245743 | ||||||
| chr1:220245857
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.116-12994C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220245857 | ||||||
| chr1:220245964
|
C | G | 1 | a0001c0001t0005g0250 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.116-13101G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220245964 | ||||||
| chr1:220246003
|
C | T | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.116-13140G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220246003 | ||||||
| chr1:220246111
|
C | T | 7 | a0001c0001t0003g0006a0001c0001t0003g0200a0001c0001t0003g0201others(4): Show | 8 | NA18944.hp1 NA18945.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.116-13248G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220246111 | ||||||
| chr1:220246231
|
A | T | 123 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0228others(120): Show | 123 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.116-13368T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220246231 | ||||||
| chr1:220246367
|
C | T | 1 | a0001c0001t0002g0284 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.116-13504G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220246367 | ||||||
| chr1:220246470
|
C | T | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.116-13607G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220246470 | ||||||
| chr1:220246471
|
G | A | 1 | a0001c0001t0002g0133 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.116-13608C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220246471 | ||||||
| chr1:220246483
|
T | C | 209 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(206): Show | 215 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.116-13620A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220246483 | ||||||
| chr1:220246543
|
G | C | 1 | a0001c0001t0017g0217 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.116-13680C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220246543 | ||||||
| chr1:220246635
|
T | C | 1 | a0001c0001t0003g0199 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.116-13772A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220246635 | ||||||
| chr1:220246642
|
T | C | 2 | a0001c0001t0001g0107a0001c0001t0001g0146 | 2 | HG00639.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.116-13779A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220246642 | ||||||
| chr1:220246669
|
A | T | 2 | a0001c0001t0001g0107a0001c0001t0001g0146 | 2 | HG00639.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.116-13806T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220246669 | ||||||
| chr1:220246677
|
A | G | 1 | a0001c0001t0005g0249 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.116-13814T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220246677 | ||||||
| chr1:220246686
|
C | T | 5 | a0001c0001t0010g0102a0001c0001t0010g0103a0001c0001t0010g0105others(2): Show | 5 | HG01258.hp1 HG01934.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-13823G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220246686 | ||||||
| chr1:220246822
|
A | T | 6 | a0001c0001t0011g0351a0001c0001t0011g0352a0001c0001t0013g0219others(3): Show | 6 | HG01243.hp2 HG02055.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-13959T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220246822 | ||||||
| chr1:220246829
|
G | C | 1 | a0001c0001t0001g0134 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.116-13966C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220246829 | ||||||
| chr1:220246906
|
A | AAAAT | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.116-14047_116-1404 others(8): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220246906 | ||||||
| chr1:220247053
|
A | G | 211 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(208): Show | 217 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.116-14190T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220247053 | ||||||
| chr1:220247082
|
T | C | 211 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(208): Show | 217 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.116-14219A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220247082 | ||||||
| chr1:220247107
|
T | C | 1 | a0001c0001t0025g0135 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.116-14244A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220247107 | ||||||
| chr1:220247401
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.116-14538G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220247401 | ||||||
| chr1:220247460
|
G | A | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.116-14597C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220247460 | ||||||
| chr1:220247598
|
G | A | 6 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0213others(3): Show | 6 | HG01891.hp2 HG02630.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-14735C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220247598 | ||||||
| chr1:220247638
|
T | C | 6 | a0001c0001t0011g0351a0001c0001t0011g0352a0001c0001t0013g0219others(3): Show | 6 | HG01243.hp2 HG02055.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-14775A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220247638 | ||||||
| chr1:220247639
|
T | C | 10 | a0002c0002t0007g0002a0002c0002t0007g0009a0002c0002t0007g0010others(7): Show | 11 | HG00639.hp1 HG01074.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.116-14776A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220247639 | ||||||
| chr1:220247698
|
A | G | 54 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0247others(51): Show | 54 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.116-14835T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220247698 | ||||||
| chr1:220247908
|
A | C | 2 | a0001c0001t0002g0235a0001c0001t0026g0224 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.116-15045T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220247908 | ||||||
| chr1:220247964
|
T | G | 69 | a0001c0001t0001g0059a0001c0001t0001g0244a0001c0001t0002g0060others(66): Show | 69 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.116-15101A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220247964 | ||||||
| chr1:220248021
|
TTA | T | 52 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0247others(49): Show | 52 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.116-15160_116-1515 others(6): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220248021 | ||||||
| chr1:220248128
|
CA | C | 23 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(20): Show | 28 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.116-15266delT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220248128 | ||||||
| chr1:220248254
|
C | T | 1 | a0001c0001t0004g0227 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.116-15391G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220248254 | ||||||
| chr1:220248314
|
C | T | 5 | a0002c0002t0007g0009a0002c0002t0007g0010a0002c0002t0007g0011others(2): Show | 5 | HG01074.hp2 HG02698.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-15451G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220248314 | ||||||
| chr1:220248613
|
G | A | 1 | a0001c0001t0002g0350 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.116-15750C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220248613 | ||||||
| chr1:220248614
|
G | GT | 49 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(46): Show | 51 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.116-15752dupA | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220248614 | ||||||
| chr1:220248614
|
G | GTT | 16 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0032others(13): Show | 16 | HG02145.hp2 HG02258.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.116-15753_116-1575 others(6): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220248614 | ||||||
| chr1:220248637
|
A | G | 6 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0213others(3): Show | 6 | HG01891.hp2 HG02630.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-15774T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220248637 | ||||||
| chr1:220248658
|
T | C | 15 | a0001c0001t0002g0294a0001c0001t0002g0302a0001c0001t0002g0303others(12): Show | 15 | HG00408.hp2 HG01952.hp2 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.116-15795A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220248658 | ||||||
| chr1:220248812
|
A | G | 1 | a0003c0003t0006g0046 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.116-15949T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220248812 | ||||||
| chr1:220249161
|
G | T | 1 | a0004c0005t0002g0295 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.116-16298C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220249161 | ||||||
| chr1:220249178
|
G | A | 2 | a0001c0001t0011g0351a0001c0001t0011g0352 | 2 | HG01243.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.116-16315C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220249178 | ||||||
| chr1:220249236
|
G | C | 6 | a0001c0001t0011g0351a0001c0001t0011g0352a0001c0001t0013g0219others(3): Show | 6 | HG01243.hp2 HG02055.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-16373C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220249236 | ||||||
| chr1:220249323
|
C | T | 1 | a0001c0001t0002g0294 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.116-16460G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220249323 | ||||||
| chr1:220249324
|
G | A | 1 | a0001c0017t0001g0234 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.116-16461C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220249324 | ||||||
| chr1:220249368
|
CTT | C | 6 | a0001c0001t0011g0351a0001c0001t0011g0352a0001c0001t0013g0219others(3): Show | 6 | HG01243.hp2 HG02055.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-16507_116-1650 others(6): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220249368 | ||||||
| chr1:220249372
|
T | C | 1 | a0001c0001t0003g0080 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.116-16509A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220249372 | ||||||
| chr1:220249513
|
C | T | 4 | a0001c0001t0002g0281a0001c0001t0002g0282a0001c0001t0002g0283others(1): Show | 4 | NA18943.hp2 NA18972.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-16650G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220249513 | ||||||
| chr1:220249875
|
G | T | 3 | a0002c0002t0008g0001a0002c0002t0008g0003a0002c0002t0008g0019 | 6 | NA18942.hp1 NA18973.hp1 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-17012C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220249875 | ||||||
| chr1:220249983
|
C | T | 1 | a0001c0001t0030g0348 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.116-17120G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220249983 | ||||||
| chr1:220250252
|
G | A | 6 | a0001c0001t0011g0351a0001c0001t0011g0352a0001c0001t0013g0219others(3): Show | 6 | HG01243.hp2 HG02055.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-17389C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220250252 | ||||||
| chr1:220250293
|
G | A | 15 | a0001c0001t0001g0047a0001c0001t0022g0209a0003c0003t0002g0053others(12): Show | 15 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.116-17430C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220250293 | ||||||
| chr1:220250655
|
A | G | 1 | a0001c0001t0001g0247 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.116-17792T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220250655 | ||||||
| chr1:220250710
|
G | C | 54 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0247others(51): Show | 54 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.116-17847C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220250710 | ||||||
| chr1:220251016
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.116-18153G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220251016 | ||||||
| chr1:220251176
|
T | C | 3 | a0001c0001t0002g0235a0001c0001t0022g0209a0001c0001t0026g0224 | 3 | HG02559.hp2 HG03471.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.116-18313A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220251176 | ||||||
| chr1:220251347
|
CAG | C | 6 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0213others(3): Show | 6 | HG01891.hp2 HG02630.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-18486_116-1848 others(6): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220251347 | ||||||
| chr1:220251493
|
T | C | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.116-18630A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220251493 | ||||||
| chr1:220251672
|
T | C | 1 | a0001c0001t0002g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.116-18809A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220251672 | ||||||
| chr1:220251979
|
C | T | 1 | a0001c0001t0004g0227 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.116-19116G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220251979 | ||||||
| chr1:220251988
|
A | G | 1 | a0001c0014t0001g0269 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.116-19125T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220251988 | ||||||
| chr1:220252093
|
C | A | 16 | a0001c0001t0001g0341a0001c0001t0009g0343a0001c0001t0009g0344others(13): Show | 17 | HG01261.hp2 HG01433.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.116-19230G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220252093 | ||||||
| chr1:220252126
|
T | C | 2 | a0001c0001t0017g0216a0001c0001t0017g0217 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.116-19263A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220252126 | ||||||
| chr1:220252152
|
G | GAA | 40 | a0001c0001t0001g0047a0001c0001t0001g0144a0001c0001t0002g0030others(37): Show | 40 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.116-19291_116-1929 others(6): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220252152 | ||||||
| chr1:220252152
|
GA | G | 11 | a0001c0001t0001g0066a0001c0001t0001g0098a0001c0001t0001g0147others(8): Show | 12 | HG00423.hp1 HG01256.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.116-19290delT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220252152 | ||||||
| chr1:220252169
|
A | G | 2 | a0001c0001t0009g0343a0001c0001t0009g0344 | 2 | HG01884.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.116-19306T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220252169 | ||||||
| chr1:220252183
|
A | G | 1 | a0001c0001t0022g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.116-19320T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220252183 | ||||||
| chr1:220252224
|
A | G | 8 | a0001c0001t0001g0100a0001c0001t0001g0360a0001c0001t0001g0361others(5): Show | 8 | HG00408.hp1 HG04204.hp2 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.116-19361T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220252224 | ||||||
| chr1:220252245
|
A | T | 1 | a0003c0003t0006g0045 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.116-19382T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220252245 | ||||||
| chr1:220252345
|
T | C | 1 | a0001c0001t0001g0341 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.116-19482A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220252345 | ||||||
| chr1:220252410
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.116-19547C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220252410 | ||||||
| chr1:220252420
|
A | T | 1 | a0001c0014t0001g0269 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.116-19557T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220252420 | ||||||
| chr1:220252448
|
A | G | 211 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(208): Show | 217 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.116-19585T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220252448 | ||||||
| chr1:220252544
|
G | A | 1 | a0001c0001t0024g0222 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.115+19679C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220252544 | ||||||
| chr1:220252568
|
G | A | 1 | a0001c0001t0001g0337 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.115+19655C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220252568 | ||||||
| chr1:220252572
|
C | T | 68 | a0001c0001t0001g0059a0001c0001t0001g0244a0001c0001t0002g0060others(65): Show | 68 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.115+19651G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220252572 | ||||||
| chr1:220252680
|
G | T | 3 | a0001c0001t0005g0096a0001c0001t0005g0099a0001c0001t0005g0154 | 3 | HG01433.hp2 HG03704.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.115+19543C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220252680 | ||||||
| chr1:220252690
|
T | C | 6 | a0001c0001t0003g0006a0001c0001t0003g0200a0001c0001t0003g0201others(3): Show | 7 | NA18944.hp1 NA18945.hp2 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+19533A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220252690 | ||||||
| chr1:220252707
|
CAGG | C | 128 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0228others(125): Show | 128 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.115+19513_115+1951 others(7): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220252707 | ||||||
| chr1:220252838
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.115+19385C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220252838 | ||||||
| chr1:220252920
|
C | T | 1 | a0001c0004t0009g0349 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.115+19303G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220252920 | ||||||
| chr1:220253184
|
A | C | 211 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(208): Show | 217 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.115+19039T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220253184 | ||||||
| chr1:220253295
|
G | A | 2 | a0001c0001t0002g0235a0001c0001t0026g0224 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.115+18928C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220253295 | ||||||
| chr1:220253436
|
A | T | 16 | a0001c0001t0001g0341a0001c0001t0009g0343a0001c0001t0009g0344others(13): Show | 17 | HG01261.hp2 HG01433.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.115+18787T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220253436 | ||||||
| chr1:220253478
|
C | T | 4 | a0002c0002t0008g0001a0002c0002t0008g0003a0002c0002t0008g0019others(1): Show | 7 | HG00558.hp1 NA18942.hp1 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.115+18745G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220253478 | ||||||
| chr1:220253484
|
G | A | 128 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0228others(125): Show | 128 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.115+18739C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220253484 | ||||||
| chr1:220253492
|
C | T | 1 | a0001c0001t0002g0350 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.115+18731G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220253492 | ||||||
| chr1:220253575
|
G | A | 3 | a0001c0001t0002g0350a0001c0001t0011g0351a0001c0001t0011g0352 | 3 | HG01243.hp2 HG02258.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.115+18648C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220253575 | ||||||
| chr1:220253576
|
C | G | 2 | a0001c0001t0005g0136a0001c0001t0005g0137 | 2 | NA18983.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.115+18647G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220253576 | ||||||
| chr1:220253660
|
G | A | 11 | a0001c0001t0003g0094a0001c0001t0004g0093a0001c0001t0005g0097others(8): Show | 11 | HG00609.hp1 NA18942.hp2 NA18953.hp1 others(8): Show |
intron_variant | MODIFIER | c.115+18563C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220253660 | ||||||
| chr1:220253765
|
G | T | 1 | a0001c0001t0024g0222 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.115+18458C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220253765 | ||||||
| chr1:220253802
|
A | C | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.115+18421T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220253802 | ||||||
| chr1:220254116
|
T | C | 1 | a0003c0003t0006g0041 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.115+18107A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220254116 | ||||||
| chr1:220254207
|
C | T | 1 | a0001c0001t0002g0350 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.115+18016G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220254207 | ||||||
| chr1:220254208
|
G | A | 1 | a0001c0001t0011g0081 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.115+18015C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220254208 | ||||||
| chr1:220254319
|
C | T | 39 | a0001c0001t0001g0047a0001c0001t0002g0030a0001c0001t0002g0031others(36): Show | 39 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.115+17904G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220254319 | ||||||
| chr1:220254320
|
G | A | 1 | a0001c0001t0003g0171 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.115+17903C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220254320 | ||||||
| chr1:220254404
|
C | G | 2 | a0001c0001t0004g0028a0001c0001t0004g0029 | 2 | HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.115+17819G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220254404 | ||||||
| chr1:220254468
|
A | G | 24 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0072others(21): Show | 24 | HG01358.hp2 HG01496.hp1 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.115+17755T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220254468 | ||||||
| chr1:220254497
|
G | A | 10 | a0002c0002t0007g0002a0002c0002t0007g0009a0002c0002t0007g0010others(7): Show | 11 | HG00639.hp1 HG01074.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.115+17726C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220254497 | ||||||
| chr1:220254615
|
A | G | 211 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(208): Show | 217 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.115+17608T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220254615 | ||||||
| chr1:220254688
|
A | G | 1 | a0001c0001t0001g0098 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.115+17535T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220254688 | ||||||
| chr1:220254714
|
C | G | 1 | a0001c0001t0003g0172 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.115+17509G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220254714 | ||||||
| chr1:220254952
|
C | CT | 18 | a0001c0001t0001g0064a0001c0001t0001g0145a0001c0001t0001g0147others(15): Show | 18 | HG00741.hp2 HG01192.hp2 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.115+17270dupA | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220254952 | ||||||
| chr1:220254952
|
CT | C | 38 | a0001c0001t0001g0047a0001c0001t0001g0062a0001c0001t0001g0143others(35): Show | 38 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.115+17270delA | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220254952 | ||||||
| chr1:220255045
|
T | G | 5 | a0001c0001t0001g0062a0001c0001t0001g0143a0001c0001t0001g0144others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+17178A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220255045 | ||||||
| chr1:220255201
|
CAAAGAAA others(4): Show |
C | 1 | a0001c0001t0004g0321 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.115+17011_115+1702 others(15): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220255201 | ||||||
| chr1:220255226
|
AAAC | A | 52 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0001g0247others(49): Show | 52 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.115+16994_115+1699 others(7): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220255226 | ||||||
| chr1:220255243
|
T | G | 1 | a0001c0001t0030g0348 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.115+16980A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220255243 | ||||||
| chr1:220255539
|
C | T | 1 | a0001c0001t0001g0341 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.115+16684G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220255539 | ||||||
| chr1:220255844
|
G | C | 6 | a0001c0001t0011g0351a0001c0001t0011g0352a0001c0001t0013g0219others(3): Show | 6 | HG01243.hp2 HG02055.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.115+16379C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220255844 | ||||||
| chr1:220256097
|
A | G | 1 | a0001c0001t0003g0171 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.115+16126T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220256097 | ||||||
| chr1:220256164
|
T | C | 1 | a0001c0001t0004g0258 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.115+16059A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220256164 | ||||||
| chr1:220256463
|
A | G | 1 | a0001c0017t0001g0234 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.115+15760T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220256463 | ||||||
| chr1:220256476
|
C | G | 211 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(208): Show | 217 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.115+15747G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220256476 | ||||||
| chr1:220256908
|
T | C | 1 | a0001c0001t0001g0341 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.115+15315A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220256908 | ||||||
| chr1:220257062
|
G | A | 1 | a0003c0003t0006g0055 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.115+15161C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220257062 | ||||||
| chr1:220257067
|
A | G | 2 | a0001c0001t0004g0259a0001c0001t0004g0260 | 2 | HG00423.hp2 HG00597.hp2 |
intron_variant | MODIFIER | c.115+15156T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220257067 | ||||||
| chr1:220257094
|
A | G | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG00621.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.115+15129T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220257094 | ||||||
| chr1:220257104
|
C | T | 21 | a0001c0001t0001g0341a0001c0001t0002g0211a0001c0001t0002g0212others(18): Show | 22 | HG01261.hp2 HG01433.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.115+15119G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220257104 | ||||||
| chr1:220257108
|
G | A | 1 | a0003c0003t0006g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.115+15115C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220257108 | ||||||
| chr1:220257235
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.115+14988C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220257235 | ||||||
| chr1:220257238
|
C | T | 1 | a0003c0003t0002g0043 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115+14985G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220257238 | ||||||
| chr1:220257382
|
A | C | 1 | a0001c0001t0002g0242 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.115+14841T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220257382 | ||||||
| chr1:220257446
|
C | G | 210 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(207): Show | 216 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.115+14777G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220257446 | ||||||
| chr1:220257564
|
G | C | 1 | a0001c0001t0001g0083 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.115+14659C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220257564 | ||||||
| chr1:220257746
|
T | C | 6 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0213others(3): Show | 6 | HG01891.hp2 HG02630.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.115+14477A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220257746 | ||||||
| chr1:220257775
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.115+14448A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220257775 | ||||||
| chr1:220258018
|
A | G | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.115+14205T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220258018 | ||||||
| chr1:220258025
|
T | C | 208 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(205): Show | 214 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(211): Show |
intron_variant | MODIFIER | c.115+14198A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220258025 | ||||||
| chr1:220258266
|
G | A | 2 | a0001c0001t0017g0216a0001c0001t0017g0217 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.115+13957C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220258266 | ||||||
| chr1:220258279
|
C | A | 1 | a0001c0001t0003g0168 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.115+13944G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220258279 | ||||||
| chr1:220258478
|
C | CA | 25 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0072others(22): Show | 25 | HG01358.hp2 HG01496.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.115+13744dupT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220258478 | ||||||
| chr1:220258488
|
C | T | 1 | a0001c0001t0003g0241 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.115+13735G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220258488 | ||||||
| chr1:220258490
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.115+13733A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220258490 | ||||||
| chr1:220258536
|
T | C | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG01074.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.115+13687A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220258536 | ||||||
| chr1:220258543
|
A | T | 55 | a0001c0001t0001g0047a0001c0001t0002g0030a0001c0001t0002g0031others(52): Show | 55 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.115+13680T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220258543 | ||||||
| chr1:220259335
|
C | T | 1 | a0001c0001t0020g0170 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.115+12888G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220259335 | ||||||
| chr1:220259392
|
C | T | 1 | a0001c0001t0001g0341 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.115+12831G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220259392 | ||||||
| chr1:220259400
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.115+12823G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220259400 | ||||||
| chr1:220259539
|
T | C | 207 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(204): Show | 213 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(210): Show |
intron_variant | MODIFIER | c.115+12684A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220259539 | ||||||
| chr1:220259672
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.115+12551T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220259672 | ||||||
| chr1:220260163
|
C | T | 211 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(208): Show | 217 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.115+12060G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220260163 | ||||||
| chr1:220260229
|
C | T | 30 | a0001c0001t0001g0047a0001c0001t0002g0280a0001c0001t0002g0281others(27): Show | 30 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.115+11994G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220260229 | ||||||
| chr1:220260312
|
CACAAT | C | 112 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0228others(109): Show | 112 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.115+11906_115+1191 others(9): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220260312 | ||||||
| chr1:220260604
|
G | T | 1 | a0001c0001t0002g0270 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.115+11619C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220260604 | ||||||
| chr1:220260728
|
C | T | 1 | a0001c0001t0004g0240 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.115+11495G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220260728 | ||||||
| chr1:220260763
|
G | A | 49 | a0001c0001t0001g0047a0001c0001t0002g0030a0001c0001t0002g0031others(46): Show | 49 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.115+11460C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220260763 | ||||||
| chr1:220260811
|
A | G | 2 | a0001c0001t0002g0211a0001c0001t0014g0210 | 2 | HG01891.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.115+11412T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220260811 | ||||||
| chr1:220260877
|
C | T | 2 | a0001c0001t0002g0205a0001c0001t0003g0169 | 2 | HG02155.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.115+11346G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220260877 | ||||||
| chr1:220261010
|
G | A | 1 | a0007c0013t0001g0150 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.115+11213C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220261010 | ||||||
| chr1:220261078
|
A | T | 1 | a0001c0001t0027g0027 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.115+11145T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220261078 | ||||||
| chr1:220261080
|
G | C | 1 | a0001c0001t0002g0315 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.115+11143C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220261080 | ||||||
| chr1:220261234
|
G | C | 1 | a0006c0010t0001g0095 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.115+10989C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220261234 | ||||||
| chr1:220261269
|
T | A | 6 | a0001c0001t0011g0351a0001c0001t0011g0352a0001c0001t0013g0219others(3): Show | 6 | HG01243.hp2 HG02055.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.115+10954A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220261269 | ||||||
| chr1:220261539
|
A | C | 6 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0213others(3): Show | 6 | HG01891.hp2 HG02630.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.115+10684T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220261539 | ||||||
| chr1:220261745
|
T | G | 1 | a0001c0001t0001g0151 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.115+10478A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220261745 | ||||||
| chr1:220261843
|
C | G | 3 | a0001c0001t0004g0237a0001c0001t0004g0238a0001c0001t0004g0239 | 3 | HG02723.hp1 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.115+10380G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220261843 | ||||||
| chr1:220261935
|
G | A | 1 | a0001c0001t0002g0316 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.115+10288C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220261935 | ||||||
| chr1:220261954
|
T | G | 4 | a0001c0001t0013g0219a0001c0001t0013g0220a0001c0001t0013g0221others(1): Show | 4 | HG02055.hp2 HG02723.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+10269A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220261954 | ||||||
| chr1:220262097
|
G | A | 1 | a0001c0001t0005g0152 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.115+10126C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220262097 | ||||||
| chr1:220262113
|
C | A | 1 | a0001c0001t0001g0153 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.115+10110G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220262113 | ||||||
| chr1:220262133
|
C | CA | 11 | a0001c0001t0001g0069a0001c0001t0001g0084a0001c0001t0001g0085others(8): Show | 11 | HG01496.hp1 HG01934.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.115+10089dupT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220262133 | ||||||
| chr1:220262133
|
CA | C | 35 | a0001c0001t0001g0025a0001c0001t0001g0090a0001c0001t0001g0091others(32): Show | 40 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.115+10089delT | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220262133 | ||||||
| chr1:220262133
|
CAA | C | 177 | a0001c0001t0001g0047a0001c0001t0001g0059a0001c0001t0001g0064others(174): Show | 178 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(175): Show |
intron_variant | MODIFIER | c.115+10088_115+1008 others(6): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220262133 | ||||||
| chr1:220262280
|
G | A | 6 | a0001c0001t0002g0275a0001c0001t0002g0276a0001c0001t0002g0277others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.115+9943C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220262280 | ||||||
| chr1:220262306
|
AAAAC | A | 17 | a0001c0001t0001g0158a0001c0001t0002g0350a0001c0001t0011g0351others(14): Show | 18 | HG00639.hp1 HG01074.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.115+9913_115+9916d others(6): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220262306 | ||||||
| chr1:220262326
|
C | A | 2 | a0001c0001t0002g0235a0001c0001t0026g0224 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.115+9897G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220262326 | ||||||
| chr1:220262330
|
C | A | 4 | a0001c0001t0002g0235a0001c0001t0026g0224a0002c0002t0007g0016others(1): Show | 4 | HG01256.hp2 HG01258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.115+9893G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220262330 | ||||||
| chr1:220262337
|
A | C | 2 | a0001c0001t0002g0235a0001c0001t0026g0224 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.115+9886T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220262337 | ||||||
| chr1:220262401
|
C | T | 211 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(208): Show | 217 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.115+9822G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220262401 | ||||||
| chr1:220262550
|
T | C | 2 | a0002c0002t0008g0020a0002c0002t0008g0021 | 2 | HG03927.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.115+9673A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220262550 | ||||||
| chr1:220262636
|
G | A | 2 | a0001c0001t0017g0216a0001c0001t0017g0217 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.115+9587C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220262636 | ||||||
| chr1:220262657
|
T | C | 56 | a0001c0001t0001g0047a0001c0001t0002g0030a0001c0001t0002g0031others(53): Show | 56 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.115+9566A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220262657 | ||||||
| chr1:220262739
|
A | G | 50 | a0001c0001t0001g0047a0001c0001t0002g0030a0001c0001t0002g0031others(47): Show | 50 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.115+9484T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220262739 | ||||||
| chr1:220262810
|
C | A | 6 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(3): Show | 7 | HG00423.hp1 HG02027.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.115+9413G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220262810 | ||||||
| chr1:220262854
|
T | A | 1 | a0001c0017t0001g0234 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.115+9369A>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220262854 | ||||||
| chr1:220262860
|
A | T | 25 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0072others(22): Show | 25 | HG01358.hp2 HG01496.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.115+9363T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220262860 | ||||||
| chr1:220262902
|
C | T | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.115+9321G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220262902 | ||||||
| chr1:220262970
|
C | CT | 57 | a0001c0001t0001g0047a0001c0001t0002g0030a0001c0001t0002g0031others(54): Show | 57 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.115+9252dupA | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220262970 | ||||||
| chr1:220262970
|
CT | C | 9 | a0001c0001t0001g0062a0001c0001t0001g0157a0001c0001t0001g0261others(6): Show | 9 | HG00558.hp1 HG02055.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.115+9252delA | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220262970 | ||||||
| chr1:220263032
|
A | C | 8 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0004g0227others(5): Show | 8 | NA18612.hp2 NA18955.hp1 NA18980.hp1 others(5): Show |
intron_variant | MODIFIER | c.115+9191T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220263032 | ||||||
| chr1:220263034
|
CACTCTGA others(4501): Show |
C | 8 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0004g0227others(5): Show | 8 | NA18612.hp2 NA18955.hp1 NA18980.hp1 others(5): Show |
intron_variant | MODIFIER | c.115+4681_115+9188d others(2): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220263034 | ||||||
| chr1:220263246
|
A | G | 1 | a0001c0001t0002g0279 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.115+8977T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220263246 | ||||||
| chr1:220263528
|
C | G | 1 | a0001c0001t0004g0236 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.115+8695G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220263528 | ||||||
| chr1:220263558
|
A | G | 2 | a0001c0001t0002g0235a0001c0001t0026g0224 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.115+8665T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220263558 | ||||||
| chr1:220263591
|
C | G | 1 | a0001c0001t0027g0027 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.115+8632G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220263591 | ||||||
| chr1:220263600
|
G | A | 203 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(200): Show | 209 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.115+8623C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220263600 | ||||||
| chr1:220263647
|
G | A | 6 | a0001c0001t0003g0263a0001c0001t0003g0265a0001c0001t0003g0266others(3): Show | 6 | HG01243.hp1 HG02717.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.115+8576C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220263647 | ||||||
| chr1:220263655
|
T | G | 1 | a0001c0001t0032g0268 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.115+8568A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220263655 | ||||||
| chr1:220263719
|
T | G | 2 | a0001c0001t0015g0339a0001c0001t0015g0340 | 2 | HG01261.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.115+8504A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220263719 | ||||||
| chr1:220264008
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.115+8215G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220264008 | ||||||
| chr1:220264025
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.115+8198G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220264025 | ||||||
| chr1:220264029
|
C | T | 18 | a0001c0001t0001g0341a0001c0001t0009g0343a0001c0001t0009g0344others(15): Show | 19 | HG01261.hp2 HG01433.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.115+8194G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220264029 | ||||||
| chr1:220264097
|
C | T | 1 | a0001c0001t0003g0168 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.115+8126G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220264097 | ||||||
| chr1:220264484
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.115+7739C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220264484 | ||||||
| chr1:220264764
|
G | C | 1 | a0001c0001t0017g0217 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.115+7459C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220264764 | ||||||
| chr1:220265003
|
T | C | 1 | a0003c0003t0006g0058 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.115+7220A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220265003 | ||||||
| chr1:220265092
|
T | C | 1 | a0001c0001t0001g0158 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.115+7131A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220265092 | ||||||
| chr1:220265163
|
A | G | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.115+7060T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220265163 | ||||||
| chr1:220265356
|
A | G | 1 | a0001c0017t0001g0234 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.115+6867T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220265356 | ||||||
| chr1:220265471
|
C | T | 2 | a0001c0001t0017g0216a0001c0001t0017g0217 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.115+6752G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220265471 | ||||||
| chr1:220265569
|
T | C | 1 | a0001c0001t0034g0370 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.115+6654A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220265569 | ||||||
| chr1:220265607
|
C | T | 6 | a0001c0001t0002g0275a0001c0001t0002g0276a0001c0001t0002g0277others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.115+6616G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220265607 | ||||||
| chr1:220265777
|
T | G | 1 | a0001c0001t0002g0206 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.115+6446A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220265777 | ||||||
| chr1:220266170
|
A | G | 3 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068 | 3 | HG00597.hp1 HG00621.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.115+6053T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220266170 | ||||||
| chr1:220266203
|
G | A | 1 | a0010c0018t0003g0207 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.115+6020C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220266203 | ||||||
| chr1:220266216
|
T | C | 1 | a0001c0001t0002g0061 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.115+6007A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220266216 | ||||||
| chr1:220266382
|
A | C | 1 | a0002c0007t0008g0018 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.115+5841T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220266382 | ||||||
| chr1:220266450
|
C | G | 1 | a0001c0017t0001g0234 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.115+5773G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220266450 | ||||||
| chr1:220266461
|
T | G | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0162others(1): Show | 4 | HG00741.hp2 HG01069.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.115+5762A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220266461 | ||||||
| chr1:220266698
|
C | T | 2 | a0001c0001t0015g0339a0001c0001t0015g0340 | 2 | HG01261.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.115+5525G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220266698 | ||||||
| chr1:220266858
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.115+5365C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220266858 | ||||||
| chr1:220267111
|
C | T | 1 | a0001c0004t0009g0338 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.115+5112G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220267111 | ||||||
| chr1:220267176
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.115+5047C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220267176 | ||||||
| chr1:220267215
|
T | C | 2 | a0001c0001t0001g0166a0005c0009t0001g0165 | 2 | NA18957.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.115+5008A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220267215 | ||||||
| chr1:220267376
|
T | G | 17 | a0001c0001t0001g0341a0001c0001t0002g0350a0001c0001t0009g0343others(14): Show | 18 | HG01261.hp2 HG01433.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.115+4847A>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220267376 | ||||||
| chr1:220267543
|
C | CT | 203 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(200): Show | 209 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.115+4679dupA | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220267543 | ||||||
| chr1:220267543
|
C | T | 8 | a0001c0001t0001g0064a0001c0001t0001g0228a0001c0001t0004g0227others(5): Show | 8 | NA18612.hp2 NA18955.hp1 NA18980.hp1 others(5): Show |
intron_variant | MODIFIER | c.115+4680G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220267543 | ||||||
| chr1:220267608
|
C | A | 1 | a0001c0001t0001g0167 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.115+4615G>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220267608 | ||||||
| chr1:220267644
|
T | C | 44 | a0001c0001t0001g0185a0001c0001t0002g0181a0001c0001t0002g0191others(41): Show | 46 | HG00544.hp1 HG00558.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.115+4579A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220267644 | ||||||
| chr1:220267711
|
T | C | 1 | a0001c0001t0004g0226 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.115+4512A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220267711 | ||||||
| chr1:220267750
|
C | T | 5 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0272others(2): Show | 5 | HG02602.hp1 NA18948.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+4473G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220267750 | ||||||
| chr1:220267879
|
A | G | 1 | a0013c0021t0001g0369 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.115+4344T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220267879 | ||||||
| chr1:220267906
|
G | A | 1 | a0001c0001t0011g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.115+4317C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220267906 | ||||||
| chr1:220268059
|
A | G | 1 | a0001c0001t0034g0370 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.115+4164T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220268059 | ||||||
| chr1:220268332
|
G | A | 1 | a0001c0001t0002g0319 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.115+3891C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220268332 | ||||||
| chr1:220268562
|
A | T | 1 | a0001c0001t0004g0226 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.115+3661T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220268562 | ||||||
| chr1:220269027
|
G | C | 53 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0272others(50): Show | 53 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.115+3196C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220269027 | ||||||
| chr1:220269183
|
G | A | 1 | a0001c0001t0016g0208 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.115+3040C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220269183 | ||||||
| chr1:220269223
|
T | C | 1 | a0001c0001t0017g0217 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.115+3000A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220269223 | ||||||
| chr1:220269296
|
A | G | 2 | a0001c0001t0017g0216a0001c0001t0017g0217 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.115+2927T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220269296 | ||||||
| chr1:220269579
|
G | A | 1 | a0001c0001t0002g0320 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.115+2644C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220269579 | ||||||
| chr1:220269670
|
T | C | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.115+2553A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220269670 | ||||||
| chr1:220269752
|
A | G | 1 | a0001c0001t0004g0225 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.115+2471T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220269752 | ||||||
| chr1:220269822
|
T | C | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.115+2401A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220269822 | ||||||
| chr1:220269886
|
G | T | 1 | a0001c0001t0026g0224 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.115+2337C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220269886 | ||||||
| chr1:220269895
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.115+2328T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220269895 | ||||||
| chr1:220270121
|
C | T | 1 | a0001c0004t0009g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.115+2102G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220270121 | ||||||
| chr1:220270251
|
A | T | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.115+1972T>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220270251 | ||||||
| chr1:220270388
|
C | G | 4 | a0001c0001t0013g0219a0001c0001t0013g0220a0001c0001t0013g0221others(1): Show | 4 | HG02055.hp2 HG02723.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+1835G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220270388 | ||||||
| chr1:220270477
|
G | A | 18 | a0001c0001t0001g0337a0001c0001t0003g0335a0001c0001t0004g0321others(15): Show | 18 | HG01346.hp2 HG01975.hp1 HG01981.hp1 others(15): Show |
intron_variant | MODIFIER | c.115+1746C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220270477 | ||||||
| chr1:220270623
|
C | T | 2 | a0001c0001t0017g0216a0001c0001t0017g0217 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.115+1600G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220270623 | ||||||
| chr1:220270654
|
C | G | 1 | a0001c0001t0004g0218 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.115+1569G>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220270654 | ||||||
| chr1:220270659
|
G | A | 16 | a0001c0001t0001g0341a0001c0001t0002g0350a0001c0001t0009g0343others(13): Show | 17 | HG01261.hp2 HG01433.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.115+1564C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220270659 | ||||||
| chr1:220270751
|
T | C | 2 | a0001c0001t0017g0216a0001c0001t0017g0217 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.115+1472A>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220270751 | ||||||
| chr1:220271091
|
G | C | 2 | a0001c0001t0011g0351a0001c0001t0011g0352 | 2 | HG01243.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.115+1132C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220271091 | ||||||
| chr1:220271191
|
A | G | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.115+1032T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220271191 | ||||||
| chr1:220271333
|
G | T | 211 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(208): Show | 217 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.115+890C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220271333 | ||||||
| chr1:220271345
|
AAAAAT | A | 169 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0059others(166): Show | 175 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.115+873_115+877del others(5): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220271345 | ||||||
| chr1:220271345
|
AAAAATAA others(3): Show |
A | 14 | a0001c0001t0001g0047a0003c0003t0002g0053a0003c0003t0002g0054others(11): Show | 14 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.115+868_115+877del others(10): Show |
RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220271345 | ||||||
| chr1:220271411
|
C | T | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.115+812G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220271411 | ||||||
| chr1:220271583
|
G | A | 211 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(208): Show | 217 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.115+640C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220271583 | ||||||
| chr1:220271665
|
A | G | 1 | a0001c0001t0001g0064 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.115+558T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220271665 | ||||||
| chr1:220271687
|
A | G | 1 | a0001c0004t0009g0063 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.115+536T>C | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220271687 | ||||||
| chr1:220271734
|
G | T | 10 | a0002c0002t0007g0002a0002c0002t0007g0009a0002c0002t0007g0010others(7): Show | 11 | HG00639.hp1 HG01074.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.115+489C>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220271734 | ||||||
| chr1:220271810
|
G | A | 2 | a0001c0001t0001g0353a0002c0002t0008g0354 | 2 | HG03688.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.115+413C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220271810 | ||||||
| chr1:220271894
|
A | C | 1 | a0001c0001t0001g0062 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.115+329T>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220271894 | ||||||
| chr1:220271905
|
G | A | 1 | a0001c0001t0001g0355 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.115+318C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220271905 | ||||||
| chr1:220271928
|
G | GT | 3 | a0001c0001t0001g0059a0001c0001t0002g0060a0001c0001t0002g0061 | 3 | HG02896.hp1 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.115+294dupA | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220271928 | ||||||
| chr1:220271952
|
G | A | 1 | a0001c0001t0005g0356 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.115+271C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220271952 | ||||||
| chr1:220271976
|
C | T | 33 | a0001c0001t0001g0047a0001c0001t0002g0030a0001c0001t0002g0031others(30): Show | 33 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.115+247G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220271976 | ||||||
| chr1:220271985
|
G | A | 1 | a0001c0001t0002g0357 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.115+238C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220271985 | ||||||
| chr1:220272005
|
G | A | 2 | a0001c0001t0003g0358a0001c0001t0003g0359 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.115+218C>T | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220272005 | ||||||
| chr1:220272013
|
G | C | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00408.hp1 NA18973.hp2 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.115+210C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220272013 | ||||||
| chr1:220272146
|
C | T | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0024others(19): Show | 27 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.115+77G>A | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220272146 | ||||||
| chr1:220272199
|
G | C | 1 | a0001c0001t0004g0367 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.115+24C>G | RAB3GAP2 | ENSG00000118873.17 | transcript | ENST00000358951.7 | protein_coding | 1/34 | chr1 | 220272199 |