Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 22930 |
|---|---|
| ensemblid | ENSG00000115839.19 |
| hgncid | 17063 |
| symbol | RAB3GAP1 |
| name | RAB3 GTPase activating protein catalytic subunit 1 |
| refseq_nuc | NM_012233.3 |
| refseq_prot | NP_036365.1 |
| ensembl_nuc | ENST00000264158.13 |
| ensembl_prot | ENSP00000264158.8 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 135052292 |
| end | 135170710 |
| strand | + |
| ver | v1.2 |
| region | chr2:135052292-135170710 |
| region5000 | chr2:135047292-135175710 |
| regionname0 | RAB3GAP1_chr2_135052292_135170710 |
| regionname5000 | RAB3GAP1_chr2_135047292_135175710 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 981 | 209 | 62 | 38 | 79 | 3 | 25 | 58 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0002 | 0/0 | 981 | 59 | 1 | 8 | 40 | 1 | 9 | 29 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0003 | 0/0 | 981 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0004 | 0/0 | 981 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0005 | 0/0 | 981 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0006 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0007 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0008 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 2946 | 176 | 51 | 26 | 78 | 1 | 20 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| c0002 | 0/0 | 2946 | 58 | 1 | 7 | 40 | 1 | 9 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| c0003 | 1/1 | 2946 | 23 | 2 | 12 | 0 | 2 | 5 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| c0004 | 0/0 | 2946 | 4 | 4 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| c0005 | 0/0 | 2946 | 4 | 4 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| c0006 | 0/0 | 2946 | 4 | 4 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| c0007 | 0/0 | 2946 | 3 | 3 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| c0008 | 0/0 | 2946 | 2 | 2 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| c0009 | 0/0 | 2946 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| c0010 | 0/0 | 2946 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| c0011 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| c0012 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| c0013 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| c0014 | 0/0 | 2946 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1946 | 119 | 12 | 24 | 62 | 3 | 16 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| t0002 | 0/0 | 1945 | 77 | 9 | 12 | 44 | 0 | 12 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| t0003 | 0/0 | 1946 | 19 | 10 | 5 | 3 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| t0004 | 0/0 | 1946 | 14 | 14 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| t0005 | 0/0 | 1944 | 9 | 1 | 4 | 3 | 1 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| t0006 | 0/0 | 1945 | 4 | 2 | 0 | 2 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| t0007 | 0/0 | 1946 | 3 | 0 | 0 | 3 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| t0008 | 0/0 | 1945 | 3 | 3 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| t0009 | 0/0 | 1945 | 3 | 3 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| t0010 | 0/0 | 1944 | 3 | 2 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| t0011 | 0/0 | 1946 | 3 | 3 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| t0012 | 0/0 | 1947 | 3 | 3 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| t0013 | 0/0 | 1947 | 3 | 3 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| t0014 | 0/0 | 1946 | 2 | 1 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| t0015 | 0/0 | 1946 | 2 | 2 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| t0016 | 0/0 | 1946 | 2 | 2 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| t0017 | 0/0 | 1946 | 2 | 0 | 0 | 2 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| t0018 | 0/0 | 1946 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| t0019 | 0/0 | 1946 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| t0020 | 0/0 | 1946 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| t0021 | 0/0 | 1945 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| t0022 | 0/0 | 1945 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| t0023 | 0/0 | 1945 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| t0024 | 0/0 | 1946 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| t0025 | 0/0 | 1946 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| t0026 | 0/0 | 1946 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0027 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0054 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2946 | 176 | 51 | 26 | 78 | 1 | 20 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0001c0003 | 1/1 | 2946 | 23 | 2 | 12 | 0 | 2 | 5 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0001c0004 | 0/0 | 2946 | 4 | 4 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0001c0007 | 0/0 | 2946 | 3 | 3 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0001c0008 | 0/0 | 2946 | 2 | 2 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0001c0009 | 0/0 | 2946 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0002c0002 | 0/0 | 2946 | 58 | 1 | 7 | 40 | 1 | 9 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0002c0010 | 0/0 | 2946 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0003c0006 | 0/0 | 2946 | 4 | 4 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0004c0005 | 0/0 | 2946 | 4 | 4 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0005c0014 | 0/0 | 2946 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0006c0013 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0007c0011 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0008c0012 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4891 | 42 | 9 | 4 | 26 | 0 | 3 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0001c0001t0002 | 0/0 | 4890 | 68 | 5 | 12 | 39 | 0 | 12 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0001c0001t0003 | 0/0 | 4891 | 19 | 10 | 5 | 3 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0001c0001t0004 | 0/0 | 4891 | 14 | 14 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0001c0001t0005 | 0/0 | 4889 | 8 | 0 | 4 | 3 | 1 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0001c0001t0006 | 0/0 | 4890 | 4 | 2 | 0 | 2 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0001c0001t0007 | 0/0 | 4891 | 3 | 0 | 0 | 3 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0001c0001t0010 | 0/0 | 4889 | 3 | 2 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0001c0001t0012 | 0/0 | 4892 | 3 | 3 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0001c0001t0014 | 0/0 | 4891 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0001c0001t0015 | 0/0 | 4891 | 2 | 2 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0001c0001t0016 | 0/0 | 4891 | 2 | 2 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0001c0001t0017 | 0/0 | 4891 | 2 | 0 | 0 | 2 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0001c0001t0018 | 0/0 | 4891 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0001c0001t0020 | 0/0 | 4891 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0001c0001t0021 | 0/0 | 4890 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0001c0001t0022 | 0/0 | 4890 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0001c0001t0023 | 0/0 | 4890 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0001c0003t0001 | 1/1 | 4891 | 23 | 2 | 12 | 0 | 2 | 5 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0001c0004t0013 | 0/0 | 4892 | 3 | 3 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0001c0004t0026 | 0/0 | 4891 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0001c0007t0002 | 0/0 | 4890 | 3 | 3 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0001c0008t0008 | 0/0 | 4890 | 2 | 2 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0001c0009t0002 | 0/0 | 4890 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0002c0002t0001 | 0/0 | 4891 | 53 | 1 | 7 | 36 | 1 | 8 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0002c0002t0002 | 0/0 | 4890 | 3 | 0 | 0 | 3 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0002c0002t0019 | 0/0 | 4891 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0002c0002t0024 | 0/0 | 4891 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0002c0010t0001 | 0/0 | 4891 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0003c0006t0002 | 0/0 | 4890 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0003c0006t0009 | 0/0 | 4890 | 3 | 3 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0004c0005t0011 | 0/0 | 4891 | 3 | 3 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0004c0005t0025 | 0/0 | 4891 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0005c0014t0002 | 0/0 | 4890 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0006c0013t0005 | 0/0 | 4889 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0007c0011t0014 | 0/0 | 4891 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| a0008c0012t0008 | 0/0 | 4890 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | copy fasta | chr2 | 135047292 | 135175710 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0005g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0005g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0005g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0005g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0005g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0005g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0005g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0005g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0006g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0006g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0006g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0007g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0007g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0007g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0010g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0010g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0010g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0012g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0012g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0012g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0014g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0015g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0015g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0016g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0016g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0017g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0017g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0018g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0020g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0021g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0022g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0001t0023g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0003t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0003t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0003t0001g0027 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0003t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0003t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0003t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0003t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0003t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0003t0001g0054 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0003t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0003t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0003t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0003t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0003t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0003t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0003t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0003t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0003t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0004t0013g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0004t0013g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0004t0013g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0004t0026g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0007t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0007t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0007t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0008t0008g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0008t0008g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0001c0009t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0019g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0002t0024g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0002c0010t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0003c0006t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0003c0006t0009g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0003c0006t0009g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0003c0006t0009g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0004c0005t0011g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0004c0005t0011g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0004c0005t0011g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0004c0005t0025g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0005c0014t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0006c0013t0005g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0007c0011t0014g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| a0008c0012t0008g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0010 | EUR | FIN | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG00280 | hp2 | a0001 | c0003 | t0001 | g0062 | EUR | FIN | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0119 | EAS | CHS | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | CHS | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0133 | EAS | CHS | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | CHS | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0097 | EAS | CHS | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG00621 | hp1 | a0001 | c0001 | t0017 | g0224 | EAS | CHS | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | CHS | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0276 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0228 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0230 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0086 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0057 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0058 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01070 | hp2 | a0001 | c0003 | t0001 | g0063 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0069 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01071 | hp2 | a0001 | c0003 | t0001 | g0056 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0125 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0240 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0127 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0068 | AMR | PUR | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0033 | AMR | CLM | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01256 | hp1 | a0001 | c0003 | t0001 | g0034 | AMR | CLM | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | CLM | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01257 | hp1 | a0001 | c0003 | t0001 | g0053 | AMR | CLM | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01257 | hp2 | a0002 | c0010 | t0001 | g0120 | AMR | CLM | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0061 | AMR | CLM | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0245 | AMR | CLM | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | CLM | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01358 | hp2 | a0001 | c0001 | t0005 | g0009 | AMR | CLM | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0007 | AMR | CLM | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0188 | AMR | CLM | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01884 | hp1 | a0001 | c0003 | t0001 | g0041 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0239 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | PEL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01928 | hp2 | a0001 | c0003 | t0001 | g0043 | AMR | PEL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0077 | AMR | PEL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0152 | AMR | PEL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01975 | hp1 | a0001 | c0003 | t0001 | g0060 | AMR | PEL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | PEL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01978 | hp1 | a0001 | c0001 | t0021 | g0229 | AMR | PEL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PEL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | PEL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0055 | AMR | PEL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | PEL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG01993 | hp2 | a0001 | c0001 | t0005 | g0014 | AMR | PEL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0258 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0128 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0110 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0101 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0117 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02132 | hp1 | a0001 | c0009 | t0002 | g0153 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | KHV | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CDX | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | CDX | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0042 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02258 | hp2 | a0003 | c0006 | t0009 | g0251 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0267 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02280 | hp2 | a0001 | c0007 | t0002 | g0020 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02293 | hp1 | a0001 | c0003 | t0001 | g0059 | AMR | PEL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02293 | hp2 | a0001 | c0001 | t0005 | g0015 | AMR | PEL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02451 | hp2 | a0001 | c0008 | t0008 | g0006 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0233 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0261 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0271 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0242 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0264 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0187 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0126 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0113 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02735 | hp2 | a0002 | c0002 | t0024 | g0108 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02809 | hp1 | a0008 | c0012 | t0008 | g0003 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02809 | hp2 | a0001 | c0001 | t0012 | g0253 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02818 | hp1 | a0001 | c0001 | t0020 | g0138 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02895 | hp1 | a0004 | c0005 | t0011 | g0219 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0270 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02896 | hp2 | a0001 | c0001 | t0015 | g0273 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02897 | hp1 | a0004 | c0005 | t0011 | g0222 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0232 | AFR | ESN | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0265 | AFR | ESN | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0259 | AFR | ESN | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0234 | AFR | ESN | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03017 | hp1 | a0001 | c0001 | t0014 | g0011 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03041 | hp1 | a0001 | c0001 | t0018 | g0074 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0277 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03130 | hp1 | a0001 | c0001 | t0012 | g0252 | AFR | ESN | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03130 | hp2 | a0001 | c0004 | t0013 | g0256 | AFR | ESN | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03195 | hp1 | a0004 | c0005 | t0025 | g0221 | AFR | ESN | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03209 | hp1 | a0001 | c0001 | t0012 | g0254 | AFR | MSL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0237 | AFR | MSL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0263 | AFR | MSL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03225 | hp2 | a0004 | c0005 | t0011 | g0220 | AFR | MSL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03239 | hp1 | a0001 | c0003 | t0001 | g0064 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0231 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | MSL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0236 | AFR | MSL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0148 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03490 | hp2 | a0001 | c0003 | t0001 | g0025 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03492 | hp1 | a0001 | c0003 | t0001 | g0026 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03516 | hp1 | a0003 | c0006 | t0009 | g0249 | AFR | ESN | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03516 | hp2 | a0007 | c0011 | t0014 | g0278 | AFR | ESN | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0266 | AFR | GWD | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03579 | hp1 | a0003 | c0006 | t0002 | g0248 | AFR | MSL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0268 | AFR | MSL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03654 | hp1 | a0001 | c0001 | t0010 | g0209 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0184 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0093 | SAS | STU | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03688 | hp2 | a0001 | c0001 | t0022 | g0175 | SAS | STU | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0115 | SAS | BEB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | BEB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0075 | SAS | BEB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03942 | hp2 | a0001 | c0001 | t0023 | g0201 | SAS | BEB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0163 | SAS | STU | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0092 | SAS | STU | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0186 | SAS | STU | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0083 | SAS | STU | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG04204 | hp1 | a0001 | c0003 | t0001 | g0035 | SAS | STU | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0140 | SAS | STU | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0118 | SAS | STU | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0164 | SAS | STU | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0262 | AFR | YRI | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18522 | hp2 | a0001 | c0008 | t0008 | g0005 | AFR | YRI | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | CHB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18747 | hp2 | a0001 | c0001 | t0006 | g0225 | EAS | CHB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18906 | hp1 | a0001 | c0001 | t0010 | g0180 | AFR | YRI | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0235 | AFR | YRI | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18947 | hp2 | a0001 | c0001 | t0007 | g0154 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18954 | hp1 | a0002 | c0002 | t0019 | g0107 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18963 | hp2 | a0005 | c0014 | t0002 | g0202 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18987 | hp2 | a0001 | c0001 | t0006 | g0274 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19002 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19006 | hp1 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19030 | hp1 | a0001 | c0001 | t0010 | g0179 | AFR | LWK | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19030 | hp2 | a0001 | c0004 | t0013 | g0246 | AFR | LWK | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19043 | hp1 | a0003 | c0006 | t0009 | g0250 | AFR | LWK | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19043 | hp2 | a0001 | c0004 | t0026 | g0255 | AFR | LWK | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19058 | hp2 | a0001 | c0001 | t0007 | g0144 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19077 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19078 | hp2 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19079 | hp1 | a0001 | c0001 | t0007 | g0145 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19084 | hp1 | a0001 | c0001 | t0017 | g0226 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0260 | AFR | YRI | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA19240 | hp2 | a0001 | c0001 | t0016 | g0241 | AFR | YRI | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ASW | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA20129 | hp2 | a0006 | c0013 | t0005 | g0004 | AFR | ASW | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0112 | EUR | TSI | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA20805 | hp2 | a0001 | c0003 | t0001 | g0085 | EUR | TSI | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA20905 | hp1 | a0001 | c0003 | t0001 | g0023 | SAS | GIH | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0162 | SAS | GIH | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02109 | hp1 | a0001 | c0001 | t0016 | g0238 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0269 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02486 | hp1 | a0001 | c0007 | t0002 | g0018 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0243 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0279 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0223 | AFR | ACB | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| HG03471 | hp2 | a0001 | c0001 | t0015 | g0272 | AFR | MSL | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | USA | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA20300 | hp2 | a0001 | c0007 | t0002 | g0019 | AFR | USA | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA21309 | hp1 | a0001 | c0004 | t0013 | g0257 | AFR | LWK | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0111 | AFR | LWK | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0027 | REF | REF | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0054 | REF | REF | RAB3GAP1_chr2_135047292_135175710 | RAB3GAP1 | chr2 | 135047292 | 135175710 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:135120839
|
G | T | 1 | a0003 | 4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
missense_variant | MODERATE | c.669G>T | p.Leu223Phe | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/24 | 685/4891 | 669/2946 | 223/981 | chr2 | 135120839 | ||
| chr2:135126200
|
A | G | 1 | a0005 | 1 | NA18963.hp2 | missense_variant | MODERATE | c.850A>G | p.Thr284Ala | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 10/24 | 866/4891 | 850/2946 | 284/981 | chr2 | 135126200 | ||
| chr2:135130027
|
C | T | 1 | a0006 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.1006C>T | p.Arg336Cys | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 12/24 | 1022/4891 | 1006/2946 | 336/981 | chr2 | 135130027 | ||
| chr2:135130711
|
C | T | 1 | a0007 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.1226C>T | p.Thr409Ile | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/24 | 1242/4891 | 1226/2946 | 409/981 | chr2 | 135130711 | ||
| chr2:135132983
|
A | G | 1 | a0004 | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.1325A>G | p.Tyr442Cys | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 14/24 | 1341/4891 | 1325/2946 | 442/981 | chr2 | 135132983 | ||
| chr2:135135802
|
A | G | 1 | a0002 | 59 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(56): Show |
missense_variant | MODERATE | c.1793A>G | p.Asn598Ser | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/24 | 1809/4891 | 1793/2946 | 598/981 | chr2 | 135135802 | ||
| chr2:135168635
|
C | T | 1 | a0008 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.2800C>T | p.Pro934Ser | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 2816/4891 | 2800/2946 | 934/981 | chr2 | 135168635 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:135093688
|
A | G | 1 | a0001c0007 | 3 | HG02280.hp2 HG02486.hp1 NA20300.hp2 |
synonymous_variant | LOW | c.357A>G | p.Val119Val | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/24 | 373/4891 | 357/2946 | 119/981 | chr2 | 135093688 | ||
| chr2:135130062
|
A | G | 2 | a0001c0008a0008c0012 | 3 | HG02451.hp2 HG02809.hp1 NA18522.hp2 |
synonymous_variant | LOW | c.1041A>G | p.Arg347Arg | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 12/24 | 1057/4891 | 1041/2946 | 347/981 | chr2 | 135130062 | ||
| chr2:135150437
|
G | A | 1 | a0001c0004 | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
synonymous_variant | LOW | c.1992G>A | p.Ser664Ser | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 18/24 | 2008/4891 | 1992/2946 | 664/981 | chr2 | 135150437 | ||
| chr2:135153852
|
T | C | 13 | a0001c0001a0001c0004a0001c0007others(10): Show | 257 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(254): Show |
synonymous_variant | LOW | c.2265T>C | p.Phe755Phe | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/24 | 2281/4891 | 2265/2946 | 755/981 | chr2 | 135153852 | ||
| chr2:135162755
|
C | T | 1 | a0001c0009 | 1 | HG02132.hp1 | synonymous_variant | LOW | c.2394C>T | p.Leu798Leu | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 21/24 | 2410/4891 | 2394/2946 | 798/981 | chr2 | 135162755 | ||
| chr2:135162824
|
C | T | 1 | a0002c0010 | 1 | HG01257.hp2 | synonymous_variant | LOW | c.2463C>T | p.Phe821Phe | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 21/24 | 2479/4891 | 2463/2946 | 821/981 | chr2 | 135162824 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:135168916
|
C | G | 2 | a0001c0004t0013a0001c0004t0026 | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*135C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 135 | chr2 | 135168916 | |||||
| chr2:135168918
|
G | GA | 1 | a0001c0001t0007 | 3 | NA18947.hp2 NA19058.hp2 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*140dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 141 | INFO_REALIGN_3_PRIME | chr2 | 135168918 | ||||
| chr2:135168951
|
C | T | 1 | a0001c0001t0017 | 2 | HG00621.hp1 NA19084.hp1 |
3_prime_UTR_variant | MODIFIER | c.*170C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 170 | chr2 | 135168951 | |||||
| chr2:135168952
|
G | A | 6 | a0001c0001t0005a0001c0001t0014a0001c0008t0008others(3): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*171G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 171 | chr2 | 135168952 | |||||
| chr2:135169033
|
T | G | 1 | a0003c0006t0009 | 3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*252T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 252 | chr2 | 135169033 | |||||
| chr2:135169036
|
T | TG | 7 | a0001c0001t0003a0001c0001t0012a0001c0001t0016others(4): Show | 33 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*261dupG | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 262 | INFO_REALIGN_3_PRIME | chr2 | 135169036 | ||||
| chr2:135169084
|
G | A | 1 | a0001c0001t0016 | 2 | HG02109.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*303G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 303 | chr2 | 135169084 | |||||
| chr2:135169185
|
C | T | 1 | a0002c0002t0024 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*404C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 404 | chr2 | 135169185 | |||||
| chr2:135169417
|
A | G | 1 | a0001c0001t0023 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*636A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 636 | chr2 | 135169417 | |||||
| chr2:135169475
|
G | A | 1 | a0001c0001t0015 | 2 | HG02896.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*694G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 694 | chr2 | 135169475 | |||||
| chr2:135169773
|
G | A | 1 | a0001c0001t0018 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*992G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 992 | chr2 | 135169773 | |||||
| chr2:135169776
|
T | C | 1 | a0004c0005t0011 | 3 | HG02895.hp1 HG02897.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*995T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 995 | chr2 | 135169776 | |||||
| chr2:135169858
|
T | C | 4 | a0001c0001t0003a0001c0001t0006a0001c0001t0016others(1): Show | 27 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1077T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 1077 | chr2 | 135169858 | |||||
| chr2:135169974
|
TA | T | 19 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(16): Show | 120 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*1208delA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 1208 | INFO_REALIGN_3_PRIME | chr2 | 135169974 | ||||
| chr2:135169974
|
TAA | T | 3 | a0001c0001t0005a0001c0001t0010a0006c0013t0005 | 12 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1207_*1208delAA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 1207 | INFO_REALIGN_3_PRIME | chr2 | 135169974 | ||||
| chr2:135170022
|
G | T | 1 | a0001c0001t0022 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1241G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 1241 | chr2 | 135170022 | |||||
| chr2:135170159
|
T | C | 2 | a0001c0001t0004a0001c0001t0015 | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1378T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 1378 | chr2 | 135170159 | |||||
| chr2:135170178
|
C | T | 1 | a0001c0001t0021 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1397C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 1397 | chr2 | 135170178 | |||||
| chr2:135170443
|
A | T | 1 | a0001c0001t0020 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1662A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 1662 | chr2 | 135170443 | |||||
| chr2:135170607
|
G | C | 1 | a0001c0001t0012 | 3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1826G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 1826 | chr2 | 135170607 | |||||
| chr2:135170621
|
G | A | 1 | a0002c0002t0019 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1840G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 24/24 | 1840 | chr2 | 135170621 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:135052540
|
C | T | 1 | a0001c0001t0003g0279 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.74+55C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135052540 | ||||||
| chr2:135052568
|
A | G | 1 | a0007c0011t0014g0278 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.74+83A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135052568 | ||||||
| chr2:135052616
|
C | T | 1 | a0001c0001t0003g0277 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.74+131C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135052616 | ||||||
| chr2:135052620
|
C | T | 3 | a0001c0001t0003g0276a0001c0001t0003g0277a0001c0001t0003g0279 | 3 | HG00639.hp1 HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.74+135C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135052620 | ||||||
| chr2:135052741
|
C | T | 2 | a0001c0001t0003g0275a0001c0001t0006g0274 | 2 | NA18987.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.74+256C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135052741 | ||||||
| chr2:135052779
|
C | T | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.74+294C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135052779 | ||||||
| chr2:135052965
|
C | T | 44 | a0001c0001t0002g0247a0001c0001t0003g0227a0001c0001t0003g0228others(41): Show | 44 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.74+480C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135052965 | ||||||
| chr2:135053059
|
A | G | 1 | a0001c0001t0001g0218 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.74+574A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135053059 | ||||||
| chr2:135053182
|
G | T | 1 | a0002c0002t0001g0217 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.74+697G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135053182 | ||||||
| chr2:135053220
|
C | T | 1 | a0002c0002t0001g0217 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.74+735C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135053220 | ||||||
| chr2:135053223
|
C | T | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.74+738C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135053223 | ||||||
| chr2:135053465
|
G | A | 1 | a0001c0001t0002g0002 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.74+980G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135053465 | ||||||
| chr2:135053618
|
T | C | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.74+1133T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135053618 | ||||||
| chr2:135053621
|
G | A | 28 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(25): Show | 28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.74+1136G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135053621 | ||||||
| chr2:135053759
|
T | TA | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.74+1280dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr2 | 135053759 | |||||
| chr2:135053950
|
G | A | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.74+1465G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135053950 | ||||||
| chr2:135054125
|
A | G | 1 | a0001c0001t0003g0245 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.74+1640A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135054125 | ||||||
| chr2:135054291
|
TAGAA | T | 3 | a0001c0004t0013g0256a0001c0004t0013g0257a0001c0004t0026g0255 | 3 | HG03130.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.74+1811_74+1814del others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr2 | 135054291 | |||||
| chr2:135054421
|
A | G | 1 | a0001c0001t0002g0216 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.74+1936A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135054421 | ||||||
| chr2:135054478
|
T | A | 2 | a0002c0002t0001g0016a0002c0002t0001g0017 | 2 | HG01993.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.74+1993T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135054478 | ||||||
| chr2:135054646
|
A | G | 3 | a0001c0001t0012g0252a0001c0001t0012g0253a0001c0001t0012g0254 | 3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.74+2161A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135054646 | ||||||
| chr2:135054703
|
G | C | 1 | a0001c0001t0003g0245 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.74+2218G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135054703 | ||||||
| chr2:135055201
|
A | G | 3 | a0003c0006t0009g0249a0003c0006t0009g0250a0003c0006t0009g0251 | 3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.74+2716A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135055201 | ||||||
| chr2:135055202
|
T | C | 3 | a0001c0007t0002g0018a0001c0007t0002g0019a0001c0007t0002g0020 | 3 | HG02280.hp2 HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.74+2717T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135055202 | ||||||
| chr2:135055255
|
C | T | 4 | a0003c0006t0002g0248a0003c0006t0009g0249a0003c0006t0009g0250others(1): Show | 4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.75-2756C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135055255 | ||||||
| chr2:135055288
|
A | G | 1 | a0002c0002t0001g0215 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.75-2723A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135055288 | ||||||
| chr2:135055299
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.75-2712C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135055299 | ||||||
| chr2:135055399
|
C | T | 154 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(151): Show | 154 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.75-2612C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135055399 | ||||||
| chr2:135055404
|
A | C | 81 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(78): Show | 81 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(78): Show |
intron_variant | MODIFIER | c.75-2607A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135055404 | ||||||
| chr2:135055625
|
C | G | 9 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(6): Show | 9 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.75-2386C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135055625 | ||||||
| chr2:135055678
|
C | CA | 30 | a0001c0001t0002g0139a0001c0001t0003g0227a0001c0001t0003g0228others(27): Show | 30 | HG00621.hp1 HG00639.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.75-2316dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr2 | 135055678 | |||||
| chr2:135055714
|
G | A | 1 | a0008c0012t0008g0003 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.75-2297G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135055714 | ||||||
| chr2:135055748
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.75-2263T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135055748 | ||||||
| chr2:135055837
|
C | CT | 154 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(151): Show | 154 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.75-2165dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr2 | 135055837 | |||||
| chr2:135055888
|
G | C | 1 | a0001c0001t0002g0140 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.75-2123G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135055888 | ||||||
| chr2:135055898
|
G | A | 4 | a0003c0006t0002g0248a0003c0006t0009g0249a0003c0006t0009g0250others(1): Show | 4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.75-2113G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135055898 | ||||||
| chr2:135055996
|
C | T | 1 | a0001c0001t0002g0002 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.75-2015C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135055996 | ||||||
| chr2:135056131
|
C | T | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.75-1880C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135056131 | ||||||
| chr2:135056135
|
C | T | 4 | a0003c0006t0002g0248a0003c0006t0009g0249a0003c0006t0009g0250others(1): Show | 4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.75-1876C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135056135 | ||||||
| chr2:135056243
|
C | T | 2 | a0001c0001t0015g0272a0001c0001t0015g0273 | 2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.75-1768C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135056243 | ||||||
| chr2:135056295
|
T | G | 24 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(21): Show | 24 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.75-1716T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135056295 | ||||||
| chr2:135056451
|
G | A | 3 | a0001c0004t0013g0256a0001c0004t0013g0257a0001c0004t0026g0255 | 3 | HG03130.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.75-1560G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135056451 | ||||||
| chr2:135056467
|
T | G | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.75-1544T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135056467 | ||||||
| chr2:135056920
|
A | C | 10 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(7): Show | 10 | HG03017.hp2 HG03654.hp1 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.75-1091A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135056920 | ||||||
| chr2:135057146
|
C | T | 154 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(151): Show | 154 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.75-865C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135057146 | ||||||
| chr2:135057304
|
G | A | 2 | a0001c0001t0002g0141a0001c0001t0002g0142 | 2 | NA18982.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.75-707G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135057304 | ||||||
| chr2:135057335
|
A | G | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.75-676A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135057335 | ||||||
| chr2:135057465
|
G | A | 4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.75-546G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135057465 | ||||||
| chr2:135057572
|
A | G | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG02027.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.75-439A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135057572 | ||||||
| chr2:135057576
|
G | T | 1 | a0002c0002t0001g0135 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.75-435G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135057576 | ||||||
| chr2:135057705
|
T | G | 1 | a0006c0013t0005g0004 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.75-306T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135057705 | ||||||
| chr2:135057793
|
A | G | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.75-218A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 2/23 | chr2 | 135057793 | ||||||
| chr2:135058236
|
A | T | 4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+150A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135058236 | ||||||
| chr2:135058261
|
T | C | 4 | a0003c0006t0002g0248a0003c0006t0009g0249a0003c0006t0009g0250others(1): Show | 4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+175T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135058261 | ||||||
| chr2:135058266
|
G | A | 3 | a0001c0001t0012g0252a0001c0001t0012g0253a0001c0001t0012g0254 | 3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.150+180G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135058266 | ||||||
| chr2:135058291
|
TTA | T | 4 | a0003c0006t0002g0248a0003c0006t0009g0249a0003c0006t0009g0250others(1): Show | 4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+213_150+214del others(2): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135058291 | |||||
| chr2:135058708
|
C | G | 1 | a0001c0001t0002g0203 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.150+622C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135058708 | ||||||
| chr2:135058725
|
A | G | 10 | a0001c0001t0003g0234a0001c0001t0003g0235a0001c0001t0003g0236others(7): Show | 10 | HG01175.hp2 HG01884.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.150+639A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135058725 | ||||||
| chr2:135058729
|
A | G | 4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+643A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135058729 | ||||||
| chr2:135058832
|
T | G | 1 | a0001c0001t0002g0204 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.150+746T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135058832 | ||||||
| chr2:135058869
|
A | G | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.150+783A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135058869 | ||||||
| chr2:135059425
|
A | G | 1 | a0001c0001t0002g0140 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.150+1339A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135059425 | ||||||
| chr2:135059833
|
G | T | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.150+1747G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135059833 | ||||||
| chr2:135060002
|
C | T | 28 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(25): Show | 28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.150+1916C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135060002 | ||||||
| chr2:135060190
|
T | C | 41 | a0001c0001t0002g0247a0001c0001t0003g0227a0001c0001t0003g0228others(38): Show | 41 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.150+2104T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135060190 | ||||||
| chr2:135060256
|
A | AT | 9 | a0001c0001t0002g0213a0001c0001t0003g0234a0001c0004t0026g0255others(6): Show | 9 | HG00438.hp2 HG02258.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.150+2191dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135060256 | |||||
| chr2:135060256
|
A | ATT | 30 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(27): Show | 30 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.150+2190_150+2191d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135060256 | |||||
| chr2:135060256
|
A | ATTTT | 7 | a0001c0001t0002g0247a0001c0004t0013g0246a0004c0005t0011g0219others(4): Show | 7 | HG01243.hp1 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.150+2188_150+2191d others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135060256 | |||||
| chr2:135060256
|
A | ATTTTT | 10 | a0001c0001t0005g0007a0001c0001t0005g0009a0001c0001t0005g0010others(7): Show | 10 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.150+2187_150+2191d others(7): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135060256 | |||||
| chr2:135060256
|
AT | A | 62 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(59): Show | 62 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(59): Show |
intron_variant | MODIFIER | c.150+2191delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135060256 | |||||
| chr2:135060344
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.150+2258C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135060344 | ||||||
| chr2:135060377
|
A | G | 4 | a0001c0001t0004g0268a0001c0001t0004g0269a0001c0001t0004g0270others(1): Show | 4 | HG02109.hp2 HG02630.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+2291A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135060377 | ||||||
| chr2:135060394
|
C | T | 10 | a0001c0001t0003g0234a0001c0001t0003g0235a0001c0001t0003g0236others(7): Show | 10 | HG01175.hp2 HG01884.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.150+2308C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135060394 | ||||||
| chr2:135060395
|
G | A | 4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+2309G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135060395 | ||||||
| chr2:135060420
|
T | G | 3 | a0001c0003t0001g0025a0001c0003t0001g0026a0001c0003t0001g0027 | 3 | HG03490.hp2 HG03492.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.150+2334T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135060420 | ||||||
| chr2:135060424
|
T | A | 1 | a0002c0002t0002g0021 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.150+2338T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135060424 | ||||||
| chr2:135060568
|
G | T | 1 | a0001c0008t0008g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.150+2482G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135060568 | ||||||
| chr2:135060711
|
A | T | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.150+2625A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135060711 | ||||||
| chr2:135060907
|
T | C | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG02886.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.150+2821T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135060907 | ||||||
| chr2:135060910
|
G | C | 1 | a0001c0001t0002g0143 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.150+2824G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135060910 | ||||||
| chr2:135060917
|
T | C | 16 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0142others(13): Show | 16 | HG00741.hp2 HG01256.hp2 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.150+2831T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135060917 | ||||||
| chr2:135060965
|
A | G | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.150+2879A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135060965 | ||||||
| chr2:135061003
|
C | CT | 207 | a0001c0001t0001g0028a0001c0001t0001g0078a0001c0001t0001g0080others(204): Show | 208 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.150+2936dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135061003 | |||||
| chr2:135061003
|
C | CTT | 11 | a0001c0001t0001g0029a0001c0001t0002g0192a0001c0001t0003g0243others(8): Show | 11 | HG02074.hp1 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.150+2935_150+2936d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135061003 | |||||
| chr2:135061023
|
A | T | 1 | a0001c0009t0002g0153 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.150+2937A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135061023 | ||||||
| chr2:135061097
|
A | G | 28 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(25): Show | 28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.150+3011A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135061097 | ||||||
| chr2:135061223
|
C | T | 4 | a0003c0006t0002g0248a0003c0006t0009g0249a0003c0006t0009g0250others(1): Show | 4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+3137C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135061223 | ||||||
| chr2:135061276
|
A | T | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.150+3190A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135061276 | ||||||
| chr2:135061337
|
C | T | 154 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(151): Show | 154 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.150+3251C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135061337 | ||||||
| chr2:135061443
|
C | T | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+3357C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135061443 | ||||||
| chr2:135061824
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.150+3738A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135061824 | ||||||
| chr2:135061835
|
T | C | 4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+3749T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135061835 | ||||||
| chr2:135061943
|
G | A | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+3857G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135061943 | ||||||
| chr2:135062183
|
G | A | 1 | a0001c0001t0018g0074 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.150+4097G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135062183 | ||||||
| chr2:135062210
|
G | A | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+4124G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135062210 | ||||||
| chr2:135062261
|
A | G | 2 | a0002c0002t0001g0126a0002c0002t0001g0127 | 2 | HG01192.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.150+4175A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135062261 | ||||||
| chr2:135062355
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.150+4269A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135062355 | ||||||
| chr2:135062885
|
G | A | 4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+4799G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135062885 | ||||||
| chr2:135063173
|
T | G | 1 | a0002c0002t0001g0075 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.150+5087T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135063173 | ||||||
| chr2:135063236
|
T | TA | 9 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(6): Show | 9 | HG02055.hp1 HG02622.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.150+5151dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135063236 | |||||
| chr2:135063317
|
T | G | 1 | a0008c0012t0008g0003 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.150+5231T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135063317 | ||||||
| chr2:135063578
|
T | G | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.150+5492T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135063578 | ||||||
| chr2:135063599
|
T | C | 1 | a0001c0001t0006g0223 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.150+5513T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135063599 | ||||||
| chr2:135063762
|
T | C | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+5676T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135063762 | ||||||
| chr2:135063769
|
T | C | 1 | a0001c0001t0003g0244 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.150+5683T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135063769 | ||||||
| chr2:135063782
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.150+5696G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135063782 | ||||||
| chr2:135063863
|
A | G | 1 | a0001c0001t0005g0015 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.150+5777A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135063863 | ||||||
| chr2:135063900
|
T | A | 1 | a0001c0001t0004g0258 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.150+5814T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135063900 | ||||||
| chr2:135064106
|
C | G | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+6020C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135064106 | ||||||
| chr2:135064234
|
C | T | 2 | a0001c0001t0003g0277a0001c0001t0003g0279 | 2 | HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.150+6148C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135064234 | ||||||
| chr2:135064259
|
A | G | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.150+6173A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135064259 | ||||||
| chr2:135064392
|
G | C | 14 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(11): Show | 14 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.150+6306G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135064392 | ||||||
| chr2:135064423
|
C | T | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+6337C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135064423 | ||||||
| chr2:135064460
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.150+6374G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135064460 | ||||||
| chr2:135064728
|
C | T | 3 | a0001c0001t0012g0252a0001c0001t0012g0253a0001c0001t0012g0254 | 3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.150+6642C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135064728 | ||||||
| chr2:135064741
|
T | C | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+6655T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135064741 | ||||||
| chr2:135064749
|
T | C | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.150+6663T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135064749 | ||||||
| chr2:135064755
|
G | GT | 86 | a0001c0001t0001g0031a0001c0001t0001g0130a0001c0001t0001g0131others(83): Show | 86 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.150+6684dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135064755 | |||||
| chr2:135064755
|
G | T | 15 | a0001c0001t0004g0258a0001c0001t0004g0260a0001c0001t0004g0261others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.150+6669G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135064755 | ||||||
| chr2:135064755
|
GT | G | 7 | a0001c0001t0003g0227a0001c0001t0003g0244a0001c0001t0003g0275others(4): Show | 7 | HG00558.hp1 HG00621.hp1 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.150+6684delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135064755 | |||||
| chr2:135064771
|
G | T | 12 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0010others(9): Show | 12 | HG00280.hp1 HG01433.hp1 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.150+6685G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135064771 | ||||||
| chr2:135064915
|
A | AT | 18 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(15): Show | 18 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.150+6843dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135064915 | |||||
| chr2:135064915
|
AT | A | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.150+6843delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135064915 | |||||
| chr2:135064941
|
G | A | 28 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(25): Show | 28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.150+6855G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135064941 | ||||||
| chr2:135064986
|
G | A | 4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+6900G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135064986 | ||||||
| chr2:135065153
|
A | G | 1 | a0008c0012t0008g0003 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.150+7067A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135065153 | ||||||
| chr2:135065421
|
G | A | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.150+7335G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135065421 | ||||||
| chr2:135065472
|
C | G | 80 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(77): Show | 80 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.150+7386C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135065472 | ||||||
| chr2:135065536
|
A | G | 1 | a0002c0002t0001g0122 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.150+7450A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135065536 | ||||||
| chr2:135065694
|
C | T | 2 | a0001c0001t0015g0272a0001c0001t0015g0273 | 2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.150+7608C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135065694 | ||||||
| chr2:135065708
|
C | T | 28 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(25): Show | 28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.150+7622C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135065708 | ||||||
| chr2:135065748
|
T | G | 1 | a0001c0001t0002g0146 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.150+7662T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135065748 | ||||||
| chr2:135065767
|
A | AT | 66 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0002g0213others(63): Show | 66 | HG00280.hp1 HG00558.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.150+7703dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135065767 | |||||
| chr2:135065767
|
AT | A | 5 | a0001c0001t0001g0032a0001c0001t0001g0159a0001c0001t0002g0158others(2): Show | 5 | HG01255.hp2 HG01346.hp1 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.150+7703delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135065767 | |||||
| chr2:135065880
|
C | G | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.150+7794C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135065880 | ||||||
| chr2:135066069
|
C | T | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+7983C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135066069 | ||||||
| chr2:135066234
|
T | A | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.150+8148T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135066234 | ||||||
| chr2:135066264
|
A | G | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.150+8178A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135066264 | ||||||
| chr2:135066618
|
G | A | 2 | a0001c0001t0002g0141a0001c0001t0002g0142 | 2 | NA18982.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.150+8532G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135066618 | ||||||
| chr2:135066627
|
C | A | 2 | a0001c0003t0001g0025a0001c0003t0001g0026 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.150+8541C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135066627 | ||||||
| chr2:135066644
|
C | T | 1 | a0008c0012t0008g0003 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.150+8558C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135066644 | ||||||
| chr2:135066675
|
G | T | 1 | a0002c0002t0001g0119 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.150+8589G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135066675 | ||||||
| chr2:135066704
|
A | T | 1 | a0001c0001t0002g0212 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.150+8618A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135066704 | ||||||
| chr2:135066795
|
A | G | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.150+8709A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135066795 | ||||||
| chr2:135066804
|
G | T | 1 | a0002c0002t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.150+8718G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135066804 | ||||||
| chr2:135066820
|
C | T | 1 | a0001c0001t0003g0233 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.150+8734C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135066820 | ||||||
| chr2:135067253
|
G | C | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.150+9167G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135067253 | ||||||
| chr2:135067504
|
T | C | 80 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(77): Show | 80 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.150+9418T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135067504 | ||||||
| chr2:135067592
|
A | G | 8 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(5): Show | 8 | HG01070.hp1 HG01192.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.150+9506A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135067592 | ||||||
| chr2:135067751
|
G | C | 2 | a0001c0001t0002g0181a0001c0001t0002g0182 | 2 | HG01070.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.150+9665G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135067751 | ||||||
| chr2:135067799
|
T | C | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.150+9713T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135067799 | ||||||
| chr2:135067998
|
C | T | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.150+9912C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135067998 | ||||||
| chr2:135068435
|
TAGACTAT others(5380): Show |
T | 1 | a0002c0002t0001g0077 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.150+10351_150+1573 others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135068435 | |||||
| chr2:135068437
|
G | C | 1 | a0006c0013t0005g0004 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.150+10351G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135068437 | ||||||
| chr2:135068482
|
G | A | 6 | a0001c0001t0001g0136a0001c0001t0001g0137a0003c0006t0002g0248others(3): Show | 6 | HG02027.hp2 HG02040.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.150+10396G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135068482 | ||||||
| chr2:135068491
|
G | A | 1 | a0002c0002t0001g0076 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.150+10405G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135068491 | ||||||
| chr2:135068491
|
G | T | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.150+10405G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135068491 | ||||||
| chr2:135068691
|
T | A | 2 | a0001c0001t0001g0078a0001c0001t0002g0079 | 2 | HG00735.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.150+10605T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135068691 | ||||||
| chr2:135068738
|
G | T | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.150+10652G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135068738 | ||||||
| chr2:135068754
|
AAAAAC | A | 5 | a0002c0002t0001g0114a0002c0002t0001g0115a0002c0002t0001g0116others(2): Show | 5 | HG02027.hp1 HG02129.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.150+10686_150+1069 others(9): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135068754 | |||||
| chr2:135068893
|
C | T | 9 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(6): Show | 9 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.150+10807C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135068893 | ||||||
| chr2:135068961
|
A | G | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.150+10875A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135068961 | ||||||
| chr2:135068966
|
T | A | 28 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(25): Show | 28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.150+10880T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135068966 | ||||||
| chr2:135069005
|
C | T | 28 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(25): Show | 28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.150+10919C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135069005 | ||||||
| chr2:135069066
|
A | G | 2 | a0001c0004t0013g0257a0001c0004t0026g0255 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.150+10980A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135069066 | ||||||
| chr2:135069249
|
C | A | 5 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0081others(2): Show | 5 | HG00735.hp1 HG01358.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.150+11163C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135069249 | ||||||
| chr2:135069294
|
G | A | 3 | a0001c0001t0012g0252a0001c0001t0012g0253a0001c0001t0012g0254 | 3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.150+11208G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135069294 | ||||||
| chr2:135069341
|
C | G | 1 | a0001c0001t0001g0072 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.150+11255C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135069341 | ||||||
| chr2:135069418
|
T | C | 1 | a0001c0001t0002g0156 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.150+11332T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135069418 | ||||||
| chr2:135069435
|
T | A | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.150+11349T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135069435 | ||||||
| chr2:135069506
|
A | G | 1 | a0006c0013t0005g0004 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.150+11420A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135069506 | ||||||
| chr2:135069590
|
A | G | 1 | a0001c0001t0003g0245 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.150+11504A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135069590 | ||||||
| chr2:135069838
|
A | G | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.150+11752A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135069838 | ||||||
| chr2:135069909
|
A | G | 1 | a0002c0002t0001g0113 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.150+11823A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135069909 | ||||||
| chr2:135070052
|
G | A | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.150+11966G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135070052 | ||||||
| chr2:135070577
|
G | A | 2 | a0001c0001t0002g0158a0001c0001t0002g0160 | 2 | NA18986.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.150+12491G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135070577 | ||||||
| chr2:135070668
|
C | T | 2 | a0002c0002t0001g0111a0002c0002t0001g0112 | 2 | NA20805.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.150+12582C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135070668 | ||||||
| chr2:135070669
|
G | A | 1 | a0002c0002t0001g0083 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.150+12583G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135070669 | ||||||
| chr2:135070741
|
G | A | 3 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0001t0002g0207 | 3 | NA18966.hp2 NA18971.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.150+12655G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135070741 | ||||||
| chr2:135070880
|
G | A | 2 | a0001c0001t0003g0235a0001c0001t0003g0236 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.150+12794G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135070880 | ||||||
| chr2:135070891
|
A | G | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.150+12805A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135070891 | ||||||
| chr2:135070896
|
T | C | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.150+12810T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135070896 | ||||||
| chr2:135071043
|
T | C | 1 | a0001c0001t0006g0225 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.150+12957T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135071043 | ||||||
| chr2:135071427
|
A | G | 28 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(25): Show | 28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.150+13341A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135071427 | ||||||
| chr2:135071474
|
C | T | 1 | a0001c0001t0004g0266 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.150+13388C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135071474 | ||||||
| chr2:135071500
|
T | G | 8 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(5): Show | 8 | HG02895.hp1 HG02897.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.150+13414T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135071500 | ||||||
| chr2:135071532
|
T | TAA | 48 | a0001c0001t0002g0247a0001c0001t0003g0228a0001c0001t0003g0230others(45): Show | 48 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.150+13459_150+1346 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135071532 | |||||
| chr2:135071714
|
A | G | 1 | a0001c0001t0002g0188 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.150+13628A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135071714 | ||||||
| chr2:135071739
|
G | A | 55 | a0001c0001t0002g0247a0001c0001t0003g0227a0001c0001t0003g0228others(52): Show | 55 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.150+13653G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135071739 | ||||||
| chr2:135071763
|
G | T | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.150+13677G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135071763 | ||||||
| chr2:135071771
|
G | A | 1 | a0001c0008t0008g0005 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.150+13685G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135071771 | ||||||
| chr2:135071858
|
C | G | 24 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(21): Show | 24 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.150+13772C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135071858 | ||||||
| chr2:135071862
|
A | G | 154 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(151): Show | 154 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.150+13776A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135071862 | ||||||
| chr2:135071904
|
ATCTT | A | 3 | a0001c0001t0010g0179a0001c0001t0010g0180a0003c0006t0002g0248 | 3 | HG03579.hp1 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.150+13840_150+1384 others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135071904 | |||||
| chr2:135071952
|
G | A | 1 | a0001c0001t0003g0237 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.150+13866G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135071952 | ||||||
| chr2:135072022
|
C | T | 60 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0070others(57): Show | 61 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.150+13936C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135072022 | ||||||
| chr2:135072077
|
T | C | 1 | a0001c0001t0004g0268 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.150+13991T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135072077 | ||||||
| chr2:135072099
|
C | T | 6 | a0001c0001t0001g0082a0002c0002t0001g0114a0002c0002t0001g0115others(3): Show | 6 | HG02027.hp1 HG02055.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.150+14013C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135072099 | ||||||
| chr2:135072630
|
T | A | 6 | a0001c0001t0001g0090a0002c0002t0001g0086a0002c0002t0001g0087others(3): Show | 6 | HG00738.hp1 NA18967.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.150+14544T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135072630 | ||||||
| chr2:135072713
|
A | G | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.150+14627A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135072713 | ||||||
| chr2:135072766
|
A | G | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+14680A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135072766 | ||||||
| chr2:135072792
|
A | G | 4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+14706A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135072792 | ||||||
| chr2:135073037
|
G | A | 1 | a0001c0001t0020g0138 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.150+14951G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135073037 | ||||||
| chr2:135073047
|
G | T | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+14961G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135073047 | ||||||
| chr2:135073207
|
G | A | 1 | a0001c0001t0002g0212 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.150+15121G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135073207 | ||||||
| chr2:135073235
|
G | A | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+15149G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135073235 | ||||||
| chr2:135073249
|
C | G | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.150+15163C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135073249 | ||||||
| chr2:135073524
|
G | T | 1 | a0002c0002t0001g0125 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.150+15438G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135073524 | ||||||
| chr2:135073690
|
C | G | 1 | a0001c0001t0001g0136 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.150+15604C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135073690 | ||||||
| chr2:135073834
|
A | G | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.150+15748A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135073834 | ||||||
| chr2:135073870
|
A | G | 3 | a0001c0001t0007g0144a0001c0001t0007g0145a0001c0001t0007g0154 | 3 | NA18947.hp2 NA19058.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.150+15784A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135073870 | ||||||
| chr2:135073902
|
C | T | 1 | a0001c0001t0005g0014 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.150+15816C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135073902 | ||||||
| chr2:135074121
|
G | A | 1 | a0001c0001t0003g0245 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.150+16035G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135074121 | ||||||
| chr2:135074278
|
T | A | 1 | a0001c0001t0002g0161 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.150+16192T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135074278 | ||||||
| chr2:135074289
|
G | A | 28 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(25): Show | 28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.150+16203G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135074289 | ||||||
| chr2:135074300
|
C | T | 1 | a0002c0002t0001g0110 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.150+16214C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135074300 | ||||||
| chr2:135074444
|
T | C | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+16358T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135074444 | ||||||
| chr2:135074561
|
T | C | 154 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(151): Show | 154 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.151-16437T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135074561 | ||||||
| chr2:135074622
|
A | G | 1 | a0001c0001t0006g0225 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.151-16376A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135074622 | ||||||
| chr2:135074624
|
A | G | 1 | a0001c0001t0006g0225 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.151-16374A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135074624 | ||||||
| chr2:135074915
|
T | C | 2 | a0001c0001t0002g0183a0001c0001t0002g0184 | 2 | HG03491.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.151-16083T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135074915 | ||||||
| chr2:135074946
|
T | G | 5 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0081others(2): Show | 5 | HG00735.hp1 HG01358.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.151-16052T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135074946 | ||||||
| chr2:135075151
|
G | A | 1 | a0006c0013t0005g0004 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.151-15847G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135075151 | ||||||
| chr2:135075195
|
C | T | 1 | a0007c0011t0014g0278 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.151-15803C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135075195 | ||||||
| chr2:135075209
|
GTTCT | G | 2 | a0001c0001t0002g0247a0002c0002t0001g0017 | 2 | HG01243.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.151-15782_151-1577 others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135075209 | |||||
| chr2:135075265
|
C | T | 1 | a0001c0001t0023g0201 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.151-15733C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135075265 | ||||||
| chr2:135075329
|
C | T | 4 | a0003c0006t0002g0248a0003c0006t0009g0249a0003c0006t0009g0250others(1): Show | 4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-15669C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135075329 | ||||||
| chr2:135075639
|
C | CT | 24 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(21): Show | 24 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.151-15348dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135075639 | |||||
| chr2:135075653
|
A | T | 1 | a0002c0002t0001g0125 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.151-15345A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135075653 | ||||||
| chr2:135075678
|
T | G | 1 | a0001c0001t0016g0241 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.151-15320T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135075678 | ||||||
| chr2:135075910
|
C | CT | 14 | a0001c0001t0001g0067a0001c0001t0001g0082a0001c0001t0002g0143others(11): Show | 14 | HG00438.hp1 HG01175.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.151-15069dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135075910 | |||||
| chr2:135075910
|
CT | C | 24 | a0001c0001t0002g0158a0001c0001t0002g0162a0001c0001t0002g0163others(21): Show | 24 | HG00280.hp1 HG00738.hp1 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.151-15069delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135075910 | |||||
| chr2:135075920
|
T | G | 1 | a0001c0001t0012g0252 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.151-15078T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135075920 | ||||||
| chr2:135075938
|
G | A | 1 | a0004c0005t0011g0220 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.151-15060G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135075938 | ||||||
| chr2:135075951
|
G | A | 80 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(77): Show | 80 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.151-15047G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135075951 | ||||||
| chr2:135075951
|
G | T | 1 | a0002c0002t0001g0109 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.151-15047G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135075951 | ||||||
| chr2:135075977
|
C | G | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.151-15021C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135075977 | ||||||
| chr2:135076006
|
G | A | 2 | a0001c0001t0002g0185a0001c0001t0002g0247 | 2 | HG01243.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.151-14992G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135076006 | ||||||
| chr2:135076190
|
G | A | 4 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0001t0002g0146others(1): Show | 4 | HG02132.hp1 NA18969.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-14808G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135076190 | ||||||
| chr2:135076240
|
C | T | 28 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(25): Show | 28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.151-14758C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135076240 | ||||||
| chr2:135076401
|
A | C | 1 | a0001c0001t0007g0154 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.151-14597A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135076401 | ||||||
| chr2:135076416
|
CATTTTT | C | 11 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(8): Show | 11 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.151-14577_151-1457 others(10): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135076416 | |||||
| chr2:135077176
|
A | T | 3 | a0001c0004t0013g0256a0001c0004t0013g0257a0001c0004t0026g0255 | 3 | HG03130.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.151-13822A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135077176 | ||||||
| chr2:135077268
|
T | TCAA | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(2): Show | 5 | HG02735.hp2 HG02886.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.151-13702_151-1370 others(7): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135077268 | |||||
| chr2:135077268
|
TCAA | T | 109 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(106): Show | 109 | HG00280.hp1 HG00438.hp1 HG00741.hp2 others(106): Show |
intron_variant | MODIFIER | c.151-13702_151-1370 others(7): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135077268 | |||||
| chr2:135077288
|
A | G | 1 | a0001c0001t0004g0259 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.151-13710A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135077288 | ||||||
| chr2:135077340
|
T | C | 3 | a0001c0001t0012g0252a0001c0001t0012g0253a0001c0001t0012g0254 | 3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.151-13658T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135077340 | ||||||
| chr2:135077416
|
G | A | 1 | a0001c0001t0005g0014 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.151-13582G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135077416 | ||||||
| chr2:135077479
|
G | C | 3 | a0001c0001t0002g0161a0001c0001t0002g0189a0001c0001t0002g0190 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-13519G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135077479 | ||||||
| chr2:135077938
|
G | C | 55 | a0001c0001t0002g0247a0001c0001t0003g0227a0001c0001t0003g0228others(52): Show | 55 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.151-13060G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135077938 | ||||||
| chr2:135078456
|
T | G | 1 | a0001c0001t0004g0260 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.151-12542T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135078456 | ||||||
| chr2:135078645
|
G | GTCCCC | 34 | a0001c0001t0001g0036a0001c0001t0003g0227a0001c0001t0003g0228others(31): Show | 34 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.151-12311_151-1230 others(9): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135078645 | |||||
| chr2:135078645
|
G | GTCCCCTC others(3): Show |
8 | a0001c0001t0002g0157a0001c0001t0002g0166a0001c0001t0002g0194others(5): Show | 8 | HG02055.hp1 HG02630.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.151-12316_151-1230 others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135078645 | |||||
| chr2:135078645
|
G | GTCCCCTC others(8): Show |
4 | a0001c0001t0003g0276a0001c0001t0004g0268a0001c0001t0004g0269others(1): Show | 4 | HG00639.hp1 HG02109.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-12321_151-1230 others(19): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135078645 | |||||
| chr2:135078645
|
G | GTCCCCTC others(43): Show |
2 | a0004c0005t0011g0219a0004c0005t0011g0222 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.151-12307_151-1230 others(54): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135078645 | |||||
| chr2:135078645
|
G | GTCCCCTC others(103): Show |
1 | a0004c0005t0025g0221 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.151-12307_151-1230 others(114): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135078645 | |||||
| chr2:135078645
|
G | GTCCCCTC others(118): Show |
1 | a0001c0004t0013g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.151-12307_151-1230 others(129): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135078645 | |||||
| chr2:135078645
|
G | GTCCCCTC others(138): Show |
1 | a0001c0004t0013g0256 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.151-12307_151-1230 others(149): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135078645 | |||||
| chr2:135078645
|
G | GTCCCCTC others(148): Show |
1 | a0004c0005t0011g0220 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.151-12307_151-1230 others(159): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135078645 | |||||
| chr2:135078645
|
GTCCCC | G | 26 | a0001c0001t0001g0066a0001c0001t0001g0132a0001c0001t0002g0181others(23): Show | 26 | HG00280.hp1 HG01070.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.151-12311_151-1230 others(9): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135078645 | |||||
| chr2:135078645
|
GTCCCCTC others(3): Show |
G | 6 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0081others(3): Show | 6 | HG00735.hp1 HG01358.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.151-12316_151-1230 others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135078645 | |||||
| chr2:135078657
|
C | CCCCTCCC others(28): Show |
1 | a0001c0001t0001g0031 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.151-12325_151-1229 others(39): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135078657 | |||||
| chr2:135078672
|
CCCCTCCC others(13): Show |
C | 4 | a0003c0006t0002g0248a0003c0006t0009g0249a0003c0006t0009g0250others(1): Show | 4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-12310_151-1229 others(24): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135078672 | |||||
| chr2:135078692
|
G | C | 35 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(32): Show | 35 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.151-12306G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135078692 | ||||||
| chr2:135078707
|
C | CCCCTCCC others(198): Show |
1 | a0001c0004t0013g0257 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.151-12291_151-1229 others(209): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135078707 | ||||||
| chr2:135078707
|
C | CCCCTCCC others(163): Show |
1 | a0001c0004t0026g0255 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.151-12291_151-1229 others(174): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135078707 | ||||||
| chr2:135078708
|
T | C | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-12290T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135078708 | ||||||
| chr2:135078712
|
T | C | 5 | a0001c0001t0002g0247a0004c0005t0011g0219a0004c0005t0011g0220others(2): Show | 5 | HG01243.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.151-12286T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135078712 | ||||||
| chr2:135078768
|
C | T | 28 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(25): Show | 28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.151-12230C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135078768 | ||||||
| chr2:135078821
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.151-12177G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135078821 | ||||||
| chr2:135078873
|
T | C | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.151-12125T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135078873 | ||||||
| chr2:135078899
|
G | A | 5 | a0001c0001t0001g0022a0001c0001t0001g0037a0001c0001t0001g0038others(2): Show | 5 | HG00609.hp1 HG02155.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.151-12099G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135078899 | ||||||
| chr2:135078906
|
C | T | 1 | a0008c0012t0008g0003 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.151-12092C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135078906 | ||||||
| chr2:135079016
|
C | T | 1 | a0001c0001t0017g0224 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.151-11982C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135079016 | ||||||
| chr2:135079028
|
C | T | 1 | a0001c0009t0002g0153 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.151-11970C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135079028 | ||||||
| chr2:135079443
|
A | G | 28 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(25): Show | 28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.151-11555A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135079443 | ||||||
| chr2:135079490
|
A | G | 3 | a0001c0001t0012g0252a0001c0001t0012g0253a0001c0001t0012g0254 | 3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.151-11508A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135079490 | ||||||
| chr2:135079748
|
A | T | 1 | a0001c0001t0002g0199 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.151-11250A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135079748 | ||||||
| chr2:135079895
|
C | T | 4 | a0003c0006t0002g0248a0003c0006t0009g0249a0003c0006t0009g0250others(1): Show | 4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-11103C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135079895 | ||||||
| chr2:135079911
|
C | T | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-11087C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135079911 | ||||||
| chr2:135079973
|
C | T | 4 | a0003c0006t0002g0248a0003c0006t0009g0249a0003c0006t0009g0250others(1): Show | 4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-11025C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135079973 | ||||||
| chr2:135079990
|
G | A | 27 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(24): Show | 27 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.151-11008G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135079990 | ||||||
| chr2:135080022
|
C | A | 28 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(25): Show | 28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.151-10976C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135080022 | ||||||
| chr2:135080053
|
C | T | 2 | a0001c0001t0015g0272a0001c0001t0015g0273 | 2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.151-10945C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135080053 | ||||||
| chr2:135080116
|
C | CA | 109 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0032others(106): Show | 110 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.151-10860dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135080116 | |||||
| chr2:135080116
|
C | CAA | 22 | a0001c0001t0001g0067a0001c0001t0002g0247a0001c0001t0003g0227others(19): Show | 22 | HG00639.hp1 HG00735.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.151-10861_151-1086 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135080116 | |||||
| chr2:135080116
|
C | CAAAA | 12 | a0001c0001t0005g0008a0001c0001t0005g0009a0001c0001t0005g0010others(9): Show | 12 | HG00280.hp1 HG01358.hp2 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.151-10863_151-1086 others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135080116 | |||||
| chr2:135080116
|
CA | C | 21 | a0001c0001t0001g0065a0001c0001t0002g0176a0001c0001t0002g0187others(18): Show | 21 | HG00558.hp2 HG02055.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.151-10860delA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135080116 | |||||
| chr2:135080336
|
C | A | 265 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0029others(262): Show | 266 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(263): Show |
intron_variant | MODIFIER | c.151-10662C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135080336 | ||||||
| chr2:135080437
|
G | A | 3 | a0001c0001t0012g0252a0001c0001t0012g0253a0001c0001t0012g0254 | 3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.151-10561G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135080437 | ||||||
| chr2:135080524
|
C | T | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-10474C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135080524 | ||||||
| chr2:135080543
|
A | G | 5 | a0001c0001t0003g0234a0001c0004t0013g0246a0001c0004t0013g0256others(2): Show | 5 | HG02965.hp2 HG03130.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.151-10455A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135080543 | ||||||
| chr2:135080837
|
C | G | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-10161C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135080837 | ||||||
| chr2:135080858
|
T | A | 1 | a0002c0002t0001g0069 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.151-10140T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135080858 | ||||||
| chr2:135080889
|
G | A | 2 | a0001c0001t0002g0141a0001c0001t0002g0142 | 2 | NA18982.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.151-10109G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135080889 | ||||||
| chr2:135081073
|
G | GCACACGT others(16): Show |
1 | a0001c0001t0022g0175 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.151-9923_151-9922i others(25): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081073 | |||||
| chr2:135081076
|
A | C | 1 | a0001c0001t0022g0175 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.151-9922A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081076 | ||||||
| chr2:135081083
|
A | G | 1 | a0001c0001t0003g0244 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.151-9915A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081083 | ||||||
| chr2:135081100
|
A | G | 40 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(37): Show | 40 | HG00438.hp1 HG01346.hp2 HG01978.hp2 others(37): Show |
intron_variant | MODIFIER | c.151-9898A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081100 | ||||||
| chr2:135081195
|
T | C | 2 | a0001c0001t0002g0189a0001c0001t0002g0190 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-9803T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081195 | ||||||
| chr2:135081255
|
C | T | 1 | a0001c0001t0004g0270 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.151-9743C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081255 | ||||||
| chr2:135081263
|
C | T | 1 | a0002c0002t0001g0109 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.151-9735C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081263 | ||||||
| chr2:135081306
|
C | CA | 9 | a0001c0001t0002g0147a0001c0001t0002g0151a0001c0001t0002g0203others(6): Show | 9 | HG00438.hp2 HG00741.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.151-9670dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081306 | |||||
| chr2:135081306
|
C | CAA | 10 | a0002c0002t0001g0024a0002c0002t0001g0069a0002c0002t0001g0094others(7): Show | 10 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(7): Show |
intron_variant | MODIFIER | c.151-9671_151-9670d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081306 | |||||
| chr2:135081306
|
C | CAAAA | 7 | a0001c0001t0002g0148a0001c0001t0002g0193a0001c0001t0003g0228others(4): Show | 7 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.151-9673_151-9670d others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081306 | |||||
| chr2:135081306
|
C | CAAAAAA | 8 | a0001c0001t0003g0227a0001c0001t0003g0231a0001c0001t0003g0236others(5): Show | 8 | HG00621.hp1 HG02486.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.151-9675_151-9670d others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081306 | |||||
| chr2:135081306
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0003g0233 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.151-9679_151-9670d others(12): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081306 | |||||
| chr2:135081319
|
A | AATATATA others(3): Show |
1 | a0001c0001t0004g0264 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.151-9678_151-9677i others(12): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081319 | |||||
| chr2:135081320
|
AAAAAAAA others(8): Show |
A | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.151-9676_151-9662d others(17): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081320 | |||||
| chr2:135081321
|
A | ATATATAT others(6): Show |
1 | a0003c0006t0009g0251 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.151-9677_151-9676i others(15): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081321 | ||||||
| chr2:135081321
|
A | T | 2 | a0001c0001t0004g0264a0001c0001t0015g0273 | 2 | HG02647.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.151-9677A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081321 | ||||||
| chr2:135081321
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0004g0267 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.151-9675_151-9664d others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081321 | |||||
| chr2:135081323
|
A | T | 10 | a0001c0001t0004g0260a0001c0001t0004g0263a0001c0001t0004g0264others(7): Show | 10 | HG02258.hp2 HG02647.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.151-9675A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081323 | ||||||
| chr2:135081323
|
AAAAAATA others(5): Show |
A | 1 | a0007c0011t0014g0278 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.151-9673_151-9662d others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081323 | |||||
| chr2:135081323
|
AAAAAATA others(7): Show |
A | 1 | a0001c0001t0004g0259 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.151-9673_151-9660d others(16): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081323 | |||||
| chr2:135081325
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0051 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.151-9672_151-9671i others(12): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081325 | |||||
| chr2:135081325
|
A | AATATATA others(5): Show |
1 | a0001c0001t0001g0052 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.151-9672_151-9671i others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081325 | |||||
| chr2:135081325
|
A | T | 21 | a0001c0001t0001g0070a0001c0001t0001g0073a0001c0001t0001g0132others(18): Show | 21 | HG00423.hp1 HG02055.hp1 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.151-9673A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081325 | ||||||
| chr2:135081327
|
A | AAAAAATA others(3): Show |
2 | a0002c0002t0001g0087a0002c0002t0001g0123 | 2 | NA18967.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.151-9670_151-9669i others(12): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081327 | |||||
| chr2:135081327
|
A | AAAAAATA others(5): Show |
1 | a0002c0002t0001g0077 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.151-9670_151-9669i others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081327 | |||||
| chr2:135081327
|
A | AAAAAATA others(9): Show |
1 | a0002c0002t0001g0086 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.151-9670_151-9669i others(18): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081327 | |||||
| chr2:135081327
|
A | AAAAT | 6 | a0001c0003t0001g0085a0002c0002t0001g0100a0002c0002t0001g0101others(3): Show | 6 | HG02080.hp2 HG02083.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.151-9670_151-9669i others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081327 | |||||
| chr2:135081327
|
A | AAAATATA others(3): Show |
5 | a0001c0001t0001g0102a0001c0003t0001g0027a0001c0003t0001g0068others(2): Show | 5 | HG01243.hp2 HG03492.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.151-9670_151-9669i others(12): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081327 | |||||
| chr2:135081327
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0137 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.151-9645_151-9636d others(12): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081327 | |||||
| chr2:135081327
|
A | AATATATA others(7): Show |
3 | a0001c0001t0001g0136a0001c0003t0001g0025a0001c0003t0001g0026 | 3 | HG02027.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.151-9649_151-9636d others(16): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081327 | |||||
| chr2:135081327
|
A | ATAT | 3 | a0001c0001t0001g0039a0002c0002t0001g0117a0002c0002t0001g0129 | 3 | HG02129.hp1 HG02129.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.151-9671_151-9670i others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081327 | ||||||
| chr2:135081327
|
A | ATATATAT others(2): Show |
3 | a0001c0001t0001g0032a0002c0002t0001g0047a0002c0002t0024g0108 | 3 | HG01346.hp1 HG02735.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.151-9671_151-9670i others(11): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081327 | ||||||
| chr2:135081327
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0048 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.151-9671_151-9670i others(13): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081327 | ||||||
| chr2:135081327
|
A | T | 36 | a0001c0001t0001g0022a0001c0001t0001g0037a0001c0001t0001g0038others(33): Show | 36 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.151-9671A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081327 | ||||||
| chr2:135081327
|
AATATATA others(7): Show |
A | 1 | a0001c0004t0013g0256 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.151-9649_151-9636d others(16): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081327 | |||||
| chr2:135081328
|
AT | A | 19 | a0001c0001t0001g0067a0001c0001t0002g0149a0001c0001t0002g0150others(16): Show | 19 | HG01257.hp1 HG01928.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.151-9669delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081328 | ||||||
| chr2:135081328
|
ATAT | A | 12 | a0001c0001t0002g0141a0001c0001t0002g0161a0001c0001t0002g0163others(9): Show | 12 | HG02559.hp2 HG02818.hp2 HG03704.hp1 others(9): Show |
intron_variant | MODIFIER | c.151-9669_151-9667d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081328 | ||||||
| chr2:135081328
|
ATATATAT | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0002g0247 | 3 | HG01243.hp1 HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.151-9669_151-9663d others(9): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081328 | ||||||
| chr2:135081328
|
ATATATAT others(4): Show |
A | 1 | a0001c0001t0012g0252 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.151-9669_151-9659d others(13): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081328 | ||||||
| chr2:135081328
|
ATATATAT others(6): Show |
A | 2 | a0001c0001t0018g0074a0001c0003t0001g0043 | 2 | HG01928.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.151-9669_151-9657d others(15): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081328 | ||||||
| chr2:135081328
|
ATATATAT others(8): Show |
A | 2 | a0001c0004t0013g0257a0001c0004t0026g0255 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.151-9669_151-9655d others(17): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081328 | ||||||
| chr2:135081328
|
ATATATAT others(50): Show |
A | 1 | a0001c0004t0013g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.151-9669_151-9613d others(59): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081328 | ||||||
| chr2:135081329
|
T | A | 93 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0159others(90): Show | 93 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.151-9669T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081329 | ||||||
| chr2:135081331
|
T | A | 98 | a0001c0001t0001g0067a0001c0001t0001g0130a0001c0001t0001g0131others(95): Show | 98 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.151-9667T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081331 | ||||||
| chr2:135081333
|
T | A | 100 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0159others(97): Show | 100 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.151-9665T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081333 | ||||||
| chr2:135081335
|
T | A | 74 | a0001c0001t0001g0159a0001c0001t0002g0139a0001c0001t0002g0140others(71): Show | 74 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(71): Show |
intron_variant | MODIFIER | c.151-9663T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081335 | ||||||
| chr2:135081337
|
T | A | 30 | a0001c0001t0001g0031a0001c0001t0001g0159a0001c0001t0002g0157others(27): Show | 30 | HG01070.hp1 HG01192.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.151-9661T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081337 | ||||||
| chr2:135081339
|
T | A | 11 | a0001c0001t0002g0161a0001c0001t0002g0163a0001c0001t0002g0181others(8): Show | 11 | HG01070.hp1 HG01192.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.151-9659T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081339 | ||||||
| chr2:135081341
|
T | A | 2 | a0001c0001t0002g0163a0001c0001t0002g0247 | 2 | HG01243.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.151-9657T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081341 | ||||||
| chr2:135081342
|
ATATATAT others(31): Show |
A | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.151-9644_151-9607d others(40): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081342 | |||||
| chr2:135081343
|
T | A | 2 | a0001c0003t0001g0043a0001c0004t0013g0256 | 2 | HG01928.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.151-9655T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081343 | ||||||
| chr2:135081344
|
A | G | 2 | a0001c0001t0012g0253a0001c0001t0012g0254 | 2 | HG02809.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.151-9654A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081344 | ||||||
| chr2:135081345
|
T | A | 3 | a0001c0004t0013g0256a0001c0004t0013g0257a0001c0004t0026g0255 | 3 | HG03130.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.151-9653T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081345 | ||||||
| chr2:135081346
|
ATATATAT others(27): Show |
A | 1 | a0002c0010t0001g0120 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.151-9640_151-9607d others(36): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081346 | |||||
| chr2:135081347
|
T | A | 3 | a0001c0004t0013g0256a0001c0004t0013g0257a0001c0004t0026g0255 | 3 | HG03130.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.151-9651T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081347 | ||||||
| chr2:135081348
|
ATATATAT others(25): Show |
A | 3 | a0001c0001t0001g0067a0001c0001t0001g0071a0002c0002t0001g0112 | 3 | HG01255.hp1 HG03540.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.151-9638_151-9607d others(34): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081348 | |||||
| chr2:135081350
|
ATATATAT others(15): Show |
A | 2 | a0001c0001t0012g0253a0001c0001t0012g0254 | 2 | HG02809.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.151-9646_151-9625d others(24): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081350 | |||||
| chr2:135081350
|
ATATATAT others(23): Show |
A | 3 | a0002c0002t0001g0111a0002c0002t0001g0126a0002c0002t0001g0127 | 3 | HG01192.hp2 HG02683.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.151-9636_151-9607d others(32): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081350 | |||||
| chr2:135081351
|
TATATATA others(7): Show |
T | 10 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(7): Show | 10 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.151-9645_151-9632d others(16): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081351 | |||||
| chr2:135081354
|
ATATATAT others(19): Show |
A | 1 | a0002c0002t0001g0092 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.151-9635_151-9610d others(28): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081354 | |||||
| chr2:135081355
|
TATATATA others(3): Show |
T | 3 | a0001c0008t0008g0005a0001c0008t0008g0006a0008c0012t0008g0003 | 3 | HG02451.hp2 HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.151-9641_151-9632d others(12): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081355 | |||||
| chr2:135081356
|
A | G | 1 | a0001c0001t0012g0252 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.151-9642A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081356 | ||||||
| chr2:135081361
|
T | C | 11 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(8): Show | 11 | HG01255.hp2 HG01346.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.151-9637T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081361 | ||||||
| chr2:135081361
|
T | TATATATA others(3): Show |
1 | a0002c0002t0001g0075 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.151-9636_151-9635i others(12): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081361 | |||||
| chr2:135081361
|
T | TATATATA others(5): Show |
1 | a0001c0001t0001g0046 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.151-9636_151-9635i others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081361 | |||||
| chr2:135081361
|
TAC | T | 10 | a0001c0001t0002g0139a0001c0001t0002g0142a0001c0001t0002g0143others(7): Show | 10 | HG01070.hp1 HG01192.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.151-9630_151-9629d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081361 | |||||
| chr2:135081361
|
TACAC | T | 46 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0155others(43): Show | 46 | HG00438.hp1 HG01243.hp1 HG01346.hp2 others(43): Show |
intron_variant | MODIFIER | c.151-9632_151-9629d others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081361 | |||||
| chr2:135081362
|
ACACACAC others(3): Show |
A | 1 | a0001c0001t0012g0252 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.151-9635_151-9626d others(12): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081362 | ||||||
| chr2:135081363
|
C | T | 75 | a0001c0001t0001g0090a0001c0001t0002g0140a0001c0001t0002g0141others(72): Show | 75 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.151-9635C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081363 | ||||||
| chr2:135081365
|
C | T | 76 | a0001c0001t0002g0139a0001c0001t0002g0140a0001c0001t0002g0141others(73): Show | 76 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.151-9633C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081365 | ||||||
| chr2:135081382
|
A | G | 28 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(25): Show | 28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.151-9616A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081382 | ||||||
| chr2:135081382
|
ATATATAT others(3): Show |
A | 3 | a0001c0001t0012g0252a0001c0001t0012g0253a0001c0001t0012g0254 | 3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.151-9608_151-9599d others(12): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135081382 | |||||
| chr2:135081387
|
T | A | 1 | a0001c0004t0013g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.151-9611T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081387 | ||||||
| chr2:135081389
|
T | A | 1 | a0001c0004t0013g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.151-9609T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081389 | ||||||
| chr2:135081392
|
G | A | 1 | a0001c0004t0013g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.151-9606G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081392 | ||||||
| chr2:135081521
|
T | C | 1 | a0001c0003t0001g0035 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.151-9477T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081521 | ||||||
| chr2:135081686
|
A | G | 1 | a0001c0001t0002g0161 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.151-9312A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081686 | ||||||
| chr2:135081919
|
T | A | 1 | a0002c0002t0024g0108 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.151-9079T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135081919 | ||||||
| chr2:135082068
|
G | A | 4 | a0003c0006t0002g0248a0003c0006t0009g0249a0003c0006t0009g0250others(1): Show | 4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-8930G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135082068 | ||||||
| chr2:135082141
|
C | CAATGAAT others(1): Show |
3 | a0001c0001t0012g0252a0001c0001t0012g0253a0001c0001t0012g0254 | 3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.151-8841_151-8834d others(10): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135082141 | |||||
| chr2:135082141
|
C | CAATGAAT others(5): Show |
5 | a0001c0001t0003g0276a0002c0002t0001g0089a0004c0005t0011g0219others(2): Show | 5 | HG00639.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.151-8845_151-8834d others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135082141 | |||||
| chr2:135082141
|
C | CAATGAAT others(9): Show |
27 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(24): Show | 27 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.151-8849_151-8834d others(18): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135082141 | |||||
| chr2:135082141
|
C | CAATGAAT others(13): Show |
2 | a0001c0001t0002g0247a0001c0001t0003g0245 | 2 | HG01243.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.151-8853_151-8834d others(22): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135082141 | |||||
| chr2:135082161
|
G | GAATA | 13 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(10): Show | 13 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.151-8826_151-8823d others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135082161 | |||||
| chr2:135082161
|
G | GAATGAAT others(5): Show |
15 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.151-8834_151-8833i others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135082161 | |||||
| chr2:135082161
|
G | GAATGAAT others(9): Show |
71 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0140others(68): Show | 71 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.151-8834_151-8833i others(18): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135082161 | |||||
| chr2:135082161
|
G | GAATGAAT others(13): Show |
14 | a0001c0001t0002g0139a0001c0001t0002g0155a0001c0001t0002g0161others(11): Show | 14 | HG01346.hp2 HG01978.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.151-8834_151-8833i others(22): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135082161 | |||||
| chr2:135082161
|
G | GAATGAAT others(17): Show |
4 | a0001c0004t0013g0256a0001c0004t0013g0257a0001c0004t0026g0255others(1): Show | 4 | HG03130.hp2 HG03579.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-8834_151-8833i others(26): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135082161 | |||||
| chr2:135082235
|
C | T | 57 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(54): Show | 57 | HG00438.hp1 HG00741.hp2 HG01256.hp2 others(54): Show |
intron_variant | MODIFIER | c.151-8763C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135082235 | ||||||
| chr2:135082386
|
A | C | 1 | a0001c0001t0001g0045 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.151-8612A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135082386 | ||||||
| chr2:135082442
|
C | CT | 7 | a0001c0001t0003g0237a0002c0002t0001g0096a0002c0002t0001g0123others(4): Show | 7 | HG00621.hp2 HG02258.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.151-8540dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135082442 | |||||
| chr2:135082442
|
CT | C | 6 | a0001c0001t0001g0137a0001c0001t0002g0141a0001c0001t0002g0247others(3): Show | 6 | HG01243.hp1 HG02040.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.151-8540delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135082442 | |||||
| chr2:135082722
|
C | T | 1 | a0001c0001t0002g0188 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.151-8276C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135082722 | ||||||
| chr2:135082912
|
C | T | 1 | a0001c0001t0003g0277 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.151-8086C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135082912 | ||||||
| chr2:135083075
|
T | A | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.151-7923T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135083075 | ||||||
| chr2:135083110
|
CAGTT | C | 3 | a0001c0001t0005g0008a0001c0001t0005g0012a0001c0001t0005g0013 | 3 | NA19002.hp1 NA19006.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.151-7887_151-7884d others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135083110 | ||||||
| chr2:135083188
|
G | C | 14 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(11): Show | 14 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.151-7810G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135083188 | ||||||
| chr2:135083257
|
C | T | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.151-7741C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135083257 | ||||||
| chr2:135083319
|
A | G | 1 | a0002c0002t0001g0076 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.151-7679A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135083319 | ||||||
| chr2:135083507
|
C | A | 2 | a0001c0001t0002g0181a0001c0001t0002g0182 | 2 | HG01070.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.151-7491C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135083507 | ||||||
| chr2:135083630
|
A | T | 29 | a0001c0001t0002g0213a0001c0001t0003g0227a0001c0001t0003g0228others(26): Show | 29 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.151-7368A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135083630 | ||||||
| chr2:135083631
|
T | A | 1 | a0002c0002t0001g0121 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.151-7367T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135083631 | ||||||
| chr2:135083758
|
C | T | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.151-7240C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135083758 | ||||||
| chr2:135083767
|
G | GT | 124 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0029others(121): Show | 125 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.151-7207dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135083767 | |||||
| chr2:135083767
|
G | GTT | 14 | a0001c0001t0001g0070a0001c0001t0001g0073a0001c0001t0001g0081others(11): Show | 14 | HG00423.hp1 HG00621.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.151-7208_151-7207d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135083767 | |||||
| chr2:135083767
|
GT | G | 49 | a0001c0001t0002g0173a0001c0001t0002g0177a0001c0001t0002g0181others(46): Show | 49 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.151-7207delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135083767 | |||||
| chr2:135083767
|
GTT | G | 5 | a0003c0006t0009g0249a0003c0006t0009g0250a0003c0006t0009g0251others(2): Show | 5 | HG02258.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.151-7208_151-7207d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135083767 | |||||
| chr2:135083906
|
A | T | 1 | a0001c0001t0002g0207 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.151-7092A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135083906 | ||||||
| chr2:135083966
|
C | T | 2 | a0001c0001t0002g0181a0001c0001t0002g0182 | 2 | HG01070.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.151-7032C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135083966 | ||||||
| chr2:135084193
|
C | T | 1 | a0002c0002t0001g0094 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.151-6805C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135084193 | ||||||
| chr2:135084207
|
T | G | 1 | a0001c0001t0002g0002 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.151-6791T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135084207 | ||||||
| chr2:135084264
|
T | C | 1 | a0002c0002t0001g0133 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.151-6734T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135084264 | ||||||
| chr2:135084443
|
T | G | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.151-6555T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135084443 | ||||||
| chr2:135084659
|
A | AGGAAATA others(8110): Show |
1 | a0001c0003t0001g0035 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.151-6326_151-6325i others(8119): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135084659 | |||||
| chr2:135084763
|
C | T | 1 | a0001c0001t0020g0138 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.151-6235C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135084763 | ||||||
| chr2:135084881
|
G | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0037a0001c0001t0001g0038 | 3 | HG00609.hp1 HG02155.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.151-6117G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135084881 | ||||||
| chr2:135084998
|
G | A | 1 | a0006c0013t0005g0004 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.151-6000G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135084998 | ||||||
| chr2:135085414
|
T | A | 1 | a0001c0001t0021g0229 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.151-5584T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135085414 | ||||||
| chr2:135085665
|
C | A | 1 | a0001c0001t0003g0276 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.151-5333C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135085665 | ||||||
| chr2:135085809
|
G | A | 2 | a0001c0003t0001g0042a0001c0003t0001g0085 | 2 | HG02258.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.151-5189G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135085809 | ||||||
| chr2:135085828
|
T | C | 4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-5170T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135085828 | ||||||
| chr2:135085858
|
C | G | 4 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0002g0170others(1): Show | 4 | HG00438.hp1 HG02040.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-5140C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135085858 | ||||||
| chr2:135085859
|
C | T | 1 | a0006c0013t0005g0004 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.151-5139C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135085859 | ||||||
| chr2:135085886
|
G | A | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.151-5112G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135085886 | ||||||
| chr2:135086116
|
A | C | 1 | a0001c0001t0006g0223 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.151-4882A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135086116 | ||||||
| chr2:135086250
|
AG | A | 3 | a0001c0004t0013g0256a0001c0004t0013g0257a0001c0004t0026g0255 | 3 | HG03130.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.151-4746delG | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135086250 | |||||
| chr2:135086383
|
G | A | 1 | a0002c0002t0001g0127 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.151-4615G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135086383 | ||||||
| chr2:135086661
|
C | CT | 20 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0001g0136others(17): Show | 20 | HG00280.hp1 HG01433.hp1 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.151-4312dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135086661 | |||||
| chr2:135086661
|
CT | C | 85 | a0001c0001t0001g0022a0001c0001t0001g0049a0001c0001t0001g0159others(82): Show | 85 | HG00438.hp1 HG00609.hp1 HG01433.hp2 others(82): Show |
intron_variant | MODIFIER | c.151-4312delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135086661 | |||||
| chr2:135086686
|
T | C | 1 | a0001c0001t0020g0138 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.151-4312T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135086686 | ||||||
| chr2:135086686
|
TC | T | 35 | a0001c0001t0002g0247a0001c0001t0003g0227a0001c0001t0003g0228others(32): Show | 35 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.151-4310delC | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135086686 | |||||
| chr2:135086687
|
C | T | 15 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(12): Show | 15 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.151-4311C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135086687 | ||||||
| chr2:135087092
|
A | G | 1 | a0002c0002t0001g0017 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.151-3906A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135087092 | ||||||
| chr2:135087282
|
C | A | 13 | a0001c0001t0001g0070a0002c0002t0001g0001a0002c0002t0001g0016others(10): Show | 14 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.151-3716C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135087282 | ||||||
| chr2:135087514
|
A | G | 4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-3484A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135087514 | ||||||
| chr2:135087534
|
T | C | 1 | a0001c0001t0002g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.151-3464T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135087534 | ||||||
| chr2:135087757
|
T | C | 1 | a0001c0001t0002g0151 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.151-3241T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135087757 | ||||||
| chr2:135087820
|
T | C | 8 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(5): Show | 8 | HG02895.hp1 HG02897.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.151-3178T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135087820 | ||||||
| chr2:135088106
|
A | C | 1 | a0002c0002t0001g0069 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.151-2892A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135088106 | ||||||
| chr2:135088295
|
A | G | 1 | a0001c0001t0003g0245 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.151-2703A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135088295 | ||||||
| chr2:135088333
|
T | C | 28 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(25): Show | 28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.151-2665T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135088333 | ||||||
| chr2:135088458
|
G | A | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.151-2540G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135088458 | ||||||
| chr2:135088478
|
C | T | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.151-2520C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135088478 | ||||||
| chr2:135088490
|
A | G | 1 | a0001c0001t0002g0206 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.151-2508A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135088490 | ||||||
| chr2:135088544
|
C | G | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-2454C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135088544 | ||||||
| chr2:135088639
|
A | G | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.151-2359A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135088639 | ||||||
| chr2:135088688
|
C | CA | 25 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(22): Show | 25 | HG01346.hp1 HG01978.hp2 HG01981.hp2 others(22): Show |
intron_variant | MODIFIER | c.151-2290dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135088688 | |||||
| chr2:135088688
|
C | CAA | 40 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(37): Show | 40 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.151-2291_151-2290d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135088688 | |||||
| chr2:135088688
|
CA | C | 17 | a0001c0001t0001g0080a0001c0001t0002g0192a0001c0001t0005g0007others(14): Show | 17 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.151-2290delA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135088688 | |||||
| chr2:135089046
|
C | A | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.151-1952C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135089046 | ||||||
| chr2:135089080
|
AAGGGGTC others(389): Show |
A | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.151-1915_151-1520d others(2): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135089080 | |||||
| chr2:135089223
|
C | T | 7 | a0001c0001t0002g0139a0001c0001t0002g0155a0001c0001t0002g0167others(4): Show | 7 | HG01346.hp2 HG01978.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.151-1775C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135089223 | ||||||
| chr2:135089526
|
T | G | 1 | a0001c0001t0002g0207 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.151-1472T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135089526 | ||||||
| chr2:135089550
|
C | T | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.151-1448C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135089550 | ||||||
| chr2:135089565
|
C | T | 4 | a0003c0006t0002g0248a0003c0006t0009g0249a0003c0006t0009g0250others(1): Show | 4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-1433C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135089565 | ||||||
| chr2:135089724
|
G | A | 7 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0001t0002g0207others(4): Show | 7 | NA18952.hp2 NA18966.hp2 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.151-1274G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135089724 | ||||||
| chr2:135089809
|
A | G | 1 | a0001c0001t0006g0223 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.151-1189A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135089809 | ||||||
| chr2:135089831
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.151-1167C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135089831 | ||||||
| chr2:135089894
|
C | T | 20 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(17): Show | 20 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.151-1104C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135089894 | ||||||
| chr2:135090124
|
A | G | 5 | a0001c0001t0002g0157a0001c0001t0002g0166a0001c0001t0002g0177others(2): Show | 5 | NA18939.hp1 NA18959.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.151-874A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135090124 | ||||||
| chr2:135090313
|
T | C | 1 | a0001c0001t0002g0161 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.151-685T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135090313 | ||||||
| chr2:135090358
|
A | G | 29 | a0001c0001t0002g0247a0001c0001t0003g0227a0001c0001t0003g0228others(26): Show | 29 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.151-640A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135090358 | ||||||
| chr2:135090585
|
TA | T | 55 | a0001c0001t0002g0247a0001c0001t0003g0227a0001c0001t0003g0228others(52): Show | 55 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.151-409delA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 135090585 | |||||
| chr2:135090943
|
A | T | 2 | a0001c0001t0015g0272a0001c0001t0015g0273 | 2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.151-55A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 3/23 | chr2 | 135090943 | ||||||
| chr2:135091205
|
G | T | 2 | a0001c0001t0002g0177a0001c0001t0002g0192 | 2 | NA18967.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.283+75G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 4/23 | chr2 | 135091205 | ||||||
| chr2:135091474
|
G | T | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.283+344G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 4/23 | chr2 | 135091474 | ||||||
| chr2:135091496
|
A | G | 1 | a0001c0001t0002g0205 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.283+366A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 4/23 | chr2 | 135091496 | ||||||
| chr2:135091497
|
GAGA | G | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.283+370_283+372del others(3): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr2 | 135091497 | |||||
| chr2:135092043
|
G | A | 151 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(148): Show | 151 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.283+913G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 4/23 | chr2 | 135092043 | ||||||
| chr2:135092177
|
G | A | 1 | a0001c0003t0001g0085 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.283+1047G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 4/23 | chr2 | 135092177 | ||||||
| chr2:135092561
|
A | G | 1 | a0001c0008t0008g0005 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.284-1054A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 4/23 | chr2 | 135092561 | ||||||
| chr2:135092562
|
A | G | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.284-1053A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 4/23 | chr2 | 135092562 | ||||||
| chr2:135092629
|
G | A | 2 | a0001c0001t0001g0159a0001c0001t0002g0216 | 2 | HG02015.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.284-986G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 4/23 | chr2 | 135092629 | ||||||
| chr2:135093042
|
A | C | 2 | a0004c0005t0011g0219a0004c0005t0011g0222 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.284-573A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 4/23 | chr2 | 135093042 | ||||||
| chr2:135093208
|
C | T | 4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-407C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 4/23 | chr2 | 135093208 | ||||||
| chr2:135093216
|
A | G | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.284-399A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 4/23 | chr2 | 135093216 | ||||||
| chr2:135093380
|
A | G | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.284-235A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 4/23 | chr2 | 135093380 | ||||||
| chr2:135093465
|
C | G | 5 | a0002c0002t0001g0114a0002c0002t0001g0115a0002c0002t0001g0116others(2): Show | 5 | HG02027.hp1 HG02129.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.284-150C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 4/23 | chr2 | 135093465 | ||||||
| chr2:135094166
|
G | GA | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.362+473_362+474ins others(1): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135094166 | ||||||
| chr2:135094167
|
G | T | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.362+474G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135094167 | ||||||
| chr2:135094169
|
G | A | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.362+476G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135094169 | ||||||
| chr2:135094371
|
G | T | 80 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(77): Show | 80 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.362+678G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135094371 | ||||||
| chr2:135094393
|
G | C | 2 | a0002c0002t0001g0088a0002c0002t0001g0089 | 2 | NA19004.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.362+700G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135094393 | ||||||
| chr2:135094592
|
T | G | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.362+899T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135094592 | ||||||
| chr2:135094597
|
A | G | 28 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(25): Show | 28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.362+904A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135094597 | ||||||
| chr2:135094762
|
G | C | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.362+1069G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135094762 | ||||||
| chr2:135095122
|
C | T | 1 | a0001c0001t0002g0186 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.362+1429C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135095122 | ||||||
| chr2:135095238
|
C | T | 14 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(11): Show | 14 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.362+1545C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135095238 | ||||||
| chr2:135095249
|
T | C | 1 | a0002c0002t0001g0100 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.362+1556T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135095249 | ||||||
| chr2:135095347
|
C | T | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.362+1654C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135095347 | ||||||
| chr2:135095711
|
T | C | 4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.362+2018T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135095711 | ||||||
| chr2:135095800
|
A | G | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.362+2107A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135095800 | ||||||
| chr2:135095817
|
C | T | 8 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(5): Show | 8 | HG01070.hp1 HG01192.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.362+2124C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135095817 | ||||||
| chr2:135095848
|
C | T | 2 | a0001c0001t0002g0181a0001c0001t0002g0182 | 2 | HG01070.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.362+2155C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135095848 | ||||||
| chr2:135096186
|
C | A | 1 | a0001c0001t0002g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.362+2493C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135096186 | ||||||
| chr2:135096237
|
C | T | 154 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(151): Show | 154 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.362+2544C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135096237 | ||||||
| chr2:135096291
|
A | G | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.362+2598A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135096291 | ||||||
| chr2:135096330
|
G | A | 80 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(77): Show | 80 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.362+2637G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135096330 | ||||||
| chr2:135096382
|
A | C | 1 | a0006c0013t0005g0004 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.362+2689A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135096382 | ||||||
| chr2:135096498
|
A | G | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.362+2805A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135096498 | ||||||
| chr2:135096588
|
C | T | 2 | a0001c0001t0015g0272a0001c0001t0015g0273 | 2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.362+2895C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135096588 | ||||||
| chr2:135096641
|
C | T | 1 | a0007c0011t0014g0278 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.362+2948C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135096641 | ||||||
| chr2:135096799
|
C | T | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.362+3106C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135096799 | ||||||
| chr2:135096949
|
T | C | 1 | a0001c0001t0003g0279 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.362+3256T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135096949 | ||||||
| chr2:135097115
|
A | G | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.362+3422A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135097115 | ||||||
| chr2:135097121
|
T | C | 1 | a0002c0002t0001g0125 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.362+3428T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135097121 | ||||||
| chr2:135097137
|
C | A | 1 | a0002c0002t0001g0122 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.362+3444C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135097137 | ||||||
| chr2:135097172
|
A | G | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.362+3479A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135097172 | ||||||
| chr2:135097216
|
C | CT | 112 | a0001c0001t0001g0030a0001c0001t0001g0159a0001c0001t0002g0002others(109): Show | 112 | HG00280.hp1 HG00438.hp1 HG00741.hp2 others(109): Show |
intron_variant | MODIFIER | c.362+3539dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135097216 | |||||
| chr2:135097216
|
C | CTT | 39 | a0001c0001t0002g0149a0001c0001t0002g0193a0001c0001t0002g0205others(36): Show | 39 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.362+3538_362+3539d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135097216 | |||||
| chr2:135097242
|
G | A | 3 | a0001c0001t0012g0252a0001c0001t0012g0253a0001c0001t0012g0254 | 3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.362+3549G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135097242 | ||||||
| chr2:135097317
|
G | A | 3 | a0001c0001t0012g0252a0001c0001t0012g0253a0001c0001t0012g0254 | 3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.362+3624G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135097317 | ||||||
| chr2:135097331
|
T | C | 80 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(77): Show | 80 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.362+3638T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135097331 | ||||||
| chr2:135097387
|
G | A | 1 | a0007c0011t0014g0278 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.362+3694G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135097387 | ||||||
| chr2:135097462
|
C | T | 1 | a0002c0002t0001g0124 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.362+3769C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135097462 | ||||||
| chr2:135097480
|
C | G | 1 | a0001c0001t0003g0234 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.362+3787C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135097480 | ||||||
| chr2:135098328
|
G | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | HG02155.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.362+4635G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135098328 | ||||||
| chr2:135098468
|
G | A | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.362+4775G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135098468 | ||||||
| chr2:135098605
|
T | G | 1 | a0001c0001t0002g0148 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.362+4912T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135098605 | ||||||
| chr2:135098640
|
A | C | 1 | a0006c0013t0005g0004 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.362+4947A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135098640 | ||||||
| chr2:135098987
|
T | A | 1 | a0001c0001t0002g0206 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.362+5294T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135098987 | ||||||
| chr2:135099096
|
T | C | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.362+5403T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135099096 | ||||||
| chr2:135099101
|
T | C | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.362+5408T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135099101 | ||||||
| chr2:135099175
|
G | A | 1 | a0001c0008t0008g0005 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.362+5482G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135099175 | ||||||
| chr2:135099431
|
C | CTG | 11 | a0001c0001t0001g0066a0001c0001t0001g0071a0001c0001t0001g0102others(8): Show | 11 | HG00438.hp2 HG00621.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.362+5772_362+5773d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135099431 | |||||
| chr2:135099431
|
C | CTGTG | 3 | a0001c0001t0001g0050a0002c0002t0001g0119a0002c0002t0001g0123 | 3 | HG00423.hp2 NA18967.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.362+5770_362+5773d others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135099431 | |||||
| chr2:135099431
|
C | CTGTGTG | 3 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0070 | 3 | HG03704.hp2 NA18970.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.362+5768_362+5773d others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135099431 | |||||
| chr2:135099431
|
CTG | C | 57 | a0001c0001t0001g0039a0001c0001t0001g0044a0001c0001t0001g0045others(54): Show | 57 | HG00280.hp1 HG00639.hp1 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.362+5772_362+5773d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135099431 | |||||
| chr2:135099431
|
CTGTG | C | 34 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0130others(31): Show | 34 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.362+5770_362+5773d others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135099431 | |||||
| chr2:135099435
|
G | C | 1 | a0001c0004t0013g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.362+5742G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135099435 | ||||||
| chr2:135099463
|
G | A | 112 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0142others(109): Show | 112 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(109): Show |
intron_variant | MODIFIER | c.362+5770G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135099463 | ||||||
| chr2:135099463
|
G | GTA | 34 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(31): Show | 34 | HG00438.hp1 HG01346.hp2 HG01978.hp2 others(31): Show |
intron_variant | MODIFIER | c.362+5771_362+5772i others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135099463 | |||||
| chr2:135099463
|
G | GTGTA | 6 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0166others(3): Show | 6 | HG02155.hp2 NA18939.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.362+5778_362+5781d others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135099463 | |||||
| chr2:135099655
|
AT | A | 19 | a0001c0001t0002g0166a0001c0001t0002g0198a0001c0001t0004g0258others(16): Show | 19 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.362+5975delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135099655 | |||||
| chr2:135099735
|
A | T | 4 | a0003c0006t0002g0248a0003c0006t0009g0249a0003c0006t0009g0250others(1): Show | 4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.362+6042A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135099735 | ||||||
| chr2:135099968
|
G | T | 41 | a0001c0001t0002g0247a0001c0001t0003g0227a0001c0001t0003g0228others(38): Show | 41 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.362+6275G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135099968 | ||||||
| chr2:135100205
|
G | T | 3 | a0001c0004t0013g0256a0001c0004t0013g0257a0001c0004t0026g0255 | 3 | HG03130.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.362+6512G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135100205 | ||||||
| chr2:135100360
|
A | G | 9 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(6): Show | 9 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.362+6667A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135100360 | ||||||
| chr2:135100398
|
C | T | 2 | a0001c0001t0002g0139a0001c0001t0002g0171 | 2 | HG02056.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.362+6705C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135100398 | ||||||
| chr2:135100629
|
A | T | 4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.362+6936A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135100629 | ||||||
| chr2:135100779
|
G | C | 3 | a0003c0006t0009g0249a0003c0006t0009g0250a0003c0006t0009g0251 | 3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.362+7086G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135100779 | ||||||
| chr2:135100910
|
T | C | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.362+7217T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135100910 | ||||||
| chr2:135101286
|
G | A | 1 | a0001c0008t0008g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.362+7593G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135101286 | ||||||
| chr2:135101587
|
A | G | 2 | a0001c0003t0001g0042a0001c0003t0001g0085 | 2 | HG02258.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.362+7894A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135101587 | ||||||
| chr2:135101686
|
A | C | 2 | a0001c0001t0002g0158a0001c0001t0002g0160 | 2 | NA18986.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.362+7993A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135101686 | ||||||
| chr2:135101795
|
T | G | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.362+8102T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135101795 | ||||||
| chr2:135101801
|
A | T | 225 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(222): Show | 226 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(223): Show |
intron_variant | MODIFIER | c.362+8108A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135101801 | ||||||
| chr2:135101858
|
C | G | 4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.362+8165C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135101858 | ||||||
| chr2:135102257
|
G | T | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.362+8564G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135102257 | ||||||
| chr2:135102342
|
A | C | 2 | a0002c0002t0001g0087a0002c0002t0001g0123 | 2 | NA18967.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.362+8649A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135102342 | ||||||
| chr2:135102350
|
A | T | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.362+8657A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135102350 | ||||||
| chr2:135102353
|
T | C | 151 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(148): Show | 151 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.362+8660T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135102353 | ||||||
| chr2:135102598
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.362+8905C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135102598 | ||||||
| chr2:135102735
|
T | G | 151 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(148): Show | 151 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.362+9042T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135102735 | ||||||
| chr2:135102777
|
A | C | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.362+9084A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135102777 | ||||||
| chr2:135102787
|
G | A | 8 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(5): Show | 8 | HG02895.hp1 HG02897.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.362+9094G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135102787 | ||||||
| chr2:135102872
|
G | A | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG02027.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.362+9179G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135102872 | ||||||
| chr2:135102883
|
C | T | 1 | a0001c0001t0005g0015 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.362+9190C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135102883 | ||||||
| chr2:135102985
|
C | T | 3 | a0003c0006t0009g0249a0003c0006t0009g0250a0003c0006t0009g0251 | 3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.362+9292C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135102985 | ||||||
| chr2:135103006
|
G | GA | 104 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0030others(101): Show | 105 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.362+9330dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103006 | |||||
| chr2:135103006
|
G | GAA | 22 | a0001c0001t0001g0029a0001c0001t0005g0007a0001c0001t0005g0008others(19): Show | 22 | HG00280.hp1 HG00423.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.362+9329_362+9330d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103006 | |||||
| chr2:135103006
|
G | GAAAAA | 12 | a0001c0001t0003g0233a0001c0001t0003g0234a0001c0001t0003g0236others(9): Show | 12 | HG01175.hp2 HG01261.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.362+9326_362+9330d others(7): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103006 | |||||
| chr2:135103006
|
G | GAAAAAA | 8 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0235others(5): Show | 8 | HG00558.hp1 HG00639.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.362+9325_362+9330d others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103006 | |||||
| chr2:135103035
|
A | AT | 25 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0044others(22): Show | 25 | HG00609.hp2 HG01070.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.362+9362dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | |||||
| chr2:135103035
|
A | ATT | 5 | a0001c0001t0012g0254a0002c0002t0001g0096a0002c0002t0001g0118others(2): Show | 5 | HG00621.hp2 HG02258.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.362+9361_362+9362d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | |||||
| chr2:135103035
|
A | ATTTTTT | 15 | a0001c0001t0002g0161a0001c0001t0002g0181a0001c0001t0002g0183others(12): Show | 15 | HG01070.hp1 HG02818.hp2 HG02895.hp1 others(12): Show |
intron_variant | MODIFIER | c.362+9357_362+9362d others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | |||||
| chr2:135103035
|
A | ATTTTTTT | 30 | a0001c0001t0002g0002a0001c0001t0002g0156a0001c0001t0002g0158others(27): Show | 30 | HG01192.hp1 HG01433.hp2 HG02040.hp1 others(27): Show |
intron_variant | MODIFIER | c.362+9356_362+9362d others(9): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | |||||
| chr2:135103035
|
A | ATTTTTTT others(1): Show |
32 | a0001c0001t0001g0159a0001c0001t0002g0139a0001c0001t0002g0142others(29): Show | 32 | HG00438.hp1 HG01256.hp2 HG01346.hp2 others(29): Show |
intron_variant | MODIFIER | c.362+9355_362+9362d others(10): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | |||||
| chr2:135103035
|
A | ATTTTTTT others(2): Show |
17 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0147others(14): Show | 17 | HG00741.hp2 HG02630.hp2 HG02895.hp2 others(14): Show |
intron_variant | MODIFIER | c.362+9354_362+9362d others(11): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | |||||
| chr2:135103035
|
A | ATTTTTTT others(3): Show |
10 | a0001c0001t0002g0194a0001c0001t0004g0258a0001c0001t0004g0261others(7): Show | 10 | HG02055.hp1 HG02109.hp2 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.362+9353_362+9362d others(12): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | |||||
| chr2:135103035
|
A | ATTTTTTT others(4): Show |
6 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(3): Show | 6 | HG01993.hp2 HG02451.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.362+9352_362+9362d others(13): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | |||||
| chr2:135103035
|
A | ATTTTTTT others(5): Show |
9 | a0001c0001t0003g0240a0001c0001t0005g0007a0001c0001t0005g0008others(6): Show | 9 | HG00280.hp1 HG01175.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.362+9351_362+9362d others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | |||||
| chr2:135103035
|
A | ATTTTTTT others(6): Show |
1 | a0001c0001t0005g0015 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.362+9350_362+9362d others(15): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | |||||
| chr2:135103035
|
A | ATTTTTTT others(7): Show |
1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.362+9349_362+9362d others(16): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | |||||
| chr2:135103035
|
A | ATTTTTTT others(11): Show |
6 | a0001c0001t0003g0230a0001c0001t0003g0231a0001c0001t0003g0232others(3): Show | 6 | HG00558.hp1 HG00735.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.362+9345_362+9362d others(20): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | |||||
| chr2:135103035
|
A | ATTTTTTT others(12): Show |
8 | a0001c0001t0003g0228a0001c0001t0003g0233a0001c0001t0003g0234others(5): Show | 8 | HG00621.hp1 HG00639.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.362+9344_362+9362d others(21): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | |||||
| chr2:135103035
|
A | ATTTTTTT others(13): Show |
8 | a0001c0001t0003g0227a0001c0001t0003g0235a0001c0001t0003g0236others(5): Show | 8 | HG01884.hp2 HG02486.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.362+9343_362+9362d others(22): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | |||||
| chr2:135103035
|
A | ATTTTTTT others(14): Show |
3 | a0001c0001t0003g0245a0001c0001t0003g0276a0001c0001t0016g0241 | 3 | HG00639.hp1 HG01261.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.362+9362_362+9363i others(23): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | |||||
| chr2:135103035
|
AT | A | 6 | a0002c0002t0001g0016a0002c0002t0001g0017a0002c0002t0001g0091others(3): Show | 6 | HG00423.hp2 HG01993.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.362+9362delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103035 | |||||
| chr2:135103060
|
C | T | 1 | a0001c0001t0002g0173 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.362+9367C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135103060 | ||||||
| chr2:135103161
|
C | T | 2 | a0001c0001t0001g0102a0001c0001t0001g0105 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.362+9468C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135103161 | ||||||
| chr2:135103394
|
C | T | 1 | a0001c0001t0014g0011 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.362+9701C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135103394 | ||||||
| chr2:135103468
|
G | A | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.363-9683G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135103468 | ||||||
| chr2:135103613
|
G | A | 1 | a0001c0001t0022g0175 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.363-9538G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135103613 | ||||||
| chr2:135103724
|
T | TG | 15 | a0001c0001t0003g0277a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.363-9425dupG | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135103724 | |||||
| chr2:135103726
|
G | C | 3 | a0003c0006t0009g0249a0003c0006t0009g0250a0003c0006t0009g0251 | 3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.363-9425G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135103726 | ||||||
| chr2:135103727
|
C | G | 55 | a0001c0001t0002g0247a0001c0001t0003g0227a0001c0001t0003g0228others(52): Show | 55 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.363-9424C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135103727 | ||||||
| chr2:135103740
|
G | A | 80 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(77): Show | 80 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.363-9411G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135103740 | ||||||
| chr2:135103917
|
C | G | 1 | a0001c0001t0002g0162 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.363-9234C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135103917 | ||||||
| chr2:135103927
|
G | C | 154 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(151): Show | 154 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.363-9224G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135103927 | ||||||
| chr2:135104361
|
A | G | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.363-8790A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135104361 | ||||||
| chr2:135104539
|
T | C | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.363-8612T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135104539 | ||||||
| chr2:135104621
|
G | A | 41 | a0001c0001t0002g0247a0001c0001t0003g0227a0001c0001t0003g0228others(38): Show | 41 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.363-8530G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135104621 | ||||||
| chr2:135104639
|
G | A | 1 | a0007c0011t0014g0278 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.363-8512G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135104639 | ||||||
| chr2:135104652
|
A | G | 1 | a0002c0002t0024g0108 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.363-8499A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135104652 | ||||||
| chr2:135104699
|
A | AAAAT | 29 | a0001c0001t0001g0032a0001c0001t0001g0065a0001c0001t0001g0071others(26): Show | 29 | HG00558.hp1 HG00558.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.363-8416_363-8413d others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135104699 | |||||
| chr2:135104699
|
A | AAAATAAA others(1): Show |
8 | a0001c0001t0003g0233a0001c0001t0003g0234a0001c0001t0003g0237others(5): Show | 8 | HG01175.hp2 HG02109.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.363-8420_363-8413d others(10): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135104699 | |||||
| chr2:135104699
|
AAAAT | A | 4 | a0001c0001t0003g0228a0001c0001t0003g0230a0001c0001t0003g0231others(1): Show | 4 | HG00639.hp2 HG00735.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.363-8416_363-8413d others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135104699 | |||||
| chr2:135104778
|
A | T | 4 | a0003c0006t0002g0248a0003c0006t0009g0249a0003c0006t0009g0250others(1): Show | 4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.363-8373A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135104778 | ||||||
| chr2:135104831
|
G | C | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.363-8320G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135104831 | ||||||
| chr2:135104851
|
G | A | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.363-8300G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135104851 | ||||||
| chr2:135104889
|
AAAAC | A | 3 | a0003c0006t0009g0249a0003c0006t0009g0250a0003c0006t0009g0251 | 3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.363-8246_363-8243d others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135104889 | |||||
| chr2:135104991
|
T | C | 2 | a0001c0001t0015g0272a0001c0001t0015g0273 | 2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.363-8160T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135104991 | ||||||
| chr2:135105174
|
G | GCTCTCC | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.363-7957_363-7952d others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135105174 | |||||
| chr2:135105174
|
GCTCTCC | G | 30 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0003g0227others(27): Show | 30 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.363-7957_363-7952d others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135105174 | |||||
| chr2:135105213
|
C | G | 1 | a0002c0002t0001g0089 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.363-7938C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105213 | ||||||
| chr2:135105234
|
T | TC | 9 | a0001c0001t0001g0082a0001c0001t0002g0212a0001c0001t0003g0245others(6): Show | 9 | HG00621.hp2 HG01175.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.363-7911dupC | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135105234 | |||||
| chr2:135105288
|
C | G | 1 | a0001c0001t0001g0214 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.363-7863C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105288 | ||||||
| chr2:135105384
|
A | C | 1 | a0001c0004t0013g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.363-7767A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105384 | ||||||
| chr2:135105443
|
G | C | 4 | a0003c0006t0002g0248a0003c0006t0009g0249a0003c0006t0009g0250others(1): Show | 4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.363-7708G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105443 | ||||||
| chr2:135105444
|
G | C | 4 | a0003c0006t0002g0248a0003c0006t0009g0249a0003c0006t0009g0250others(1): Show | 4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.363-7707G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105444 | ||||||
| chr2:135105445
|
G | C | 4 | a0003c0006t0002g0248a0003c0006t0009g0249a0003c0006t0009g0250others(1): Show | 4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.363-7706G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105445 | ||||||
| chr2:135105486
|
G | T | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.363-7665G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105486 | ||||||
| chr2:135105522
|
G | A | 1 | a0001c0001t0003g0276 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.363-7629G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105522 | ||||||
| chr2:135105573
|
G | A | 151 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(148): Show | 151 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.363-7578G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105573 | ||||||
| chr2:135105577
|
C | T | 1 | a0001c0001t0002g0203 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.363-7574C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105577 | ||||||
| chr2:135105578
|
G | A | 1 | a0002c0002t0001g0125 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.363-7573G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105578 | ||||||
| chr2:135105600
|
C | T | 2 | a0001c0001t0001g0036a0001c0008t0008g0005 | 2 | HG03704.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.363-7551C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105600 | ||||||
| chr2:135105616
|
C | G | 2 | a0002c0002t0001g0126a0002c0002t0001g0127 | 2 | HG01192.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.363-7535C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105616 | ||||||
| chr2:135105719
|
T | C | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG02886.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.363-7432T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105719 | ||||||
| chr2:135105750
|
C | T | 1 | a0001c0001t0003g0233 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.363-7401C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105750 | ||||||
| chr2:135105821
|
G | A | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.363-7330G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105821 | ||||||
| chr2:135105843
|
C | T | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.363-7308C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105843 | ||||||
| chr2:135105889
|
A | G | 55 | a0001c0001t0002g0247a0001c0001t0003g0227a0001c0001t0003g0228others(52): Show | 55 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.363-7262A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105889 | ||||||
| chr2:135105907
|
A | G | 28 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(25): Show | 28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.363-7244A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105907 | ||||||
| chr2:135105946
|
C | T | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.363-7205C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135105946 | ||||||
| chr2:135106041
|
G | A | 1 | a0002c0002t0001g0129 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.363-7110G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106041 | ||||||
| chr2:135106042
|
C | T | 1 | a0001c0001t0020g0138 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.363-7109C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106042 | ||||||
| chr2:135106121
|
C | A | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.363-7030C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106121 | ||||||
| chr2:135106146
|
G | C | 3 | a0001c0001t0002g0169a0001c0001t0002g0170a0001c0001t0002g0178 | 3 | HG00438.hp1 NA18954.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.363-7005G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106146 | ||||||
| chr2:135106199
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | NA18992.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.363-6952G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106199 | ||||||
| chr2:135106236
|
C | T | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.363-6915C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106236 | ||||||
| chr2:135106240
|
A | AC | 35 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0001g0073others(32): Show | 35 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.363-6907dupC | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135106240 | |||||
| chr2:135106265
|
A | C | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.363-6886A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106265 | ||||||
| chr2:135106292
|
A | G | 28 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(25): Show | 28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.363-6859A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106292 | ||||||
| chr2:135106295
|
G | T | 1 | a0001c0004t0013g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.363-6856G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106295 | ||||||
| chr2:135106441
|
A | G | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.363-6710A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106441 | ||||||
| chr2:135106458
|
C | G | 1 | a0001c0001t0002g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.363-6693C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106458 | ||||||
| chr2:135106464
|
C | T | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.363-6687C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106464 | ||||||
| chr2:135106515
|
G | A | 2 | a0001c0001t0012g0252a0001c0001t0012g0253 | 2 | HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.363-6636G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106515 | ||||||
| chr2:135106577
|
C | T | 6 | a0001c0001t0002g0139a0001c0001t0002g0155a0001c0001t0002g0167others(3): Show | 6 | HG01346.hp2 HG01978.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.363-6574C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106577 | ||||||
| chr2:135106693
|
A | T | 12 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(9): Show | 12 | HG03017.hp2 HG03654.hp1 HG03704.hp1 others(9): Show |
intron_variant | MODIFIER | c.363-6458A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106693 | ||||||
| chr2:135106724
|
C | G | 154 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(151): Show | 154 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.363-6427C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106724 | ||||||
| chr2:135106756
|
T | TA | 81 | a0001c0001t0002g0002a0001c0001t0002g0139a0001c0001t0002g0140others(78): Show | 81 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(78): Show |
intron_variant | MODIFIER | c.363-6384dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135106756 | |||||
| chr2:135106760
|
AAAAAAAA others(1): Show |
A | 9 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(6): Show | 9 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.363-6376_363-6369d others(10): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135106760 | |||||
| chr2:135106762
|
A | T | 1 | a0001c0001t0003g0276 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.363-6389A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106762 | ||||||
| chr2:135106767
|
AT | A | 3 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0026g0255 | 3 | HG03130.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.363-6383delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106767 | ||||||
| chr2:135106771
|
A | T | 1 | a0001c0004t0013g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.363-6380A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106771 | ||||||
| chr2:135106823
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.363-6328A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106823 | ||||||
| chr2:135106827
|
G | C | 10 | a0001c0001t0003g0234a0001c0001t0003g0235a0001c0001t0003g0236others(7): Show | 10 | HG01175.hp2 HG01884.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.363-6324G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135106827 | ||||||
| chr2:135107028
|
C | G | 1 | a0001c0001t0003g0276 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.363-6123C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135107028 | ||||||
| chr2:135107098
|
G | GA | 6 | a0001c0001t0002g0143a0001c0001t0003g0275a0001c0003t0001g0055others(3): Show | 6 | HG01981.hp2 HG02486.hp1 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.363-6038dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135107098 | |||||
| chr2:135107098
|
GA | G | 7 | a0001c0001t0003g0279a0001c0001t0005g0013a0001c0001t0006g0223others(4): Show | 7 | HG02559.hp1 HG02559.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.363-6038delA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135107098 | |||||
| chr2:135107098
|
GAA | G | 13 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(10): Show | 13 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.363-6039_363-6038d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135107098 | |||||
| chr2:135107246
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.363-5905G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135107246 | ||||||
| chr2:135107383
|
CAT | C | 41 | a0001c0001t0002g0247a0001c0001t0003g0227a0001c0001t0003g0228others(38): Show | 41 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.363-5765_363-5764d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135107383 | |||||
| chr2:135107419
|
AAAGG | A | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.363-5727_363-5724d others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135107419 | |||||
| chr2:135107587
|
T | C | 3 | a0001c0001t0012g0252a0001c0001t0012g0253a0001c0001t0012g0254 | 3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.363-5564T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135107587 | ||||||
| chr2:135107644
|
A | G | 1 | a0001c0001t0003g0245 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.363-5507A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135107644 | ||||||
| chr2:135107801
|
C | T | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.363-5350C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135107801 | ||||||
| chr2:135107953
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0071 | 2 | HG01255.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.363-5198C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135107953 | ||||||
| chr2:135107975
|
CA | C | 83 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0029others(80): Show | 84 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.363-5149delA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135107975 | |||||
| chr2:135107975
|
CAA | C | 9 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0002g0079others(6): Show | 9 | HG00735.hp1 HG01192.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.363-5150_363-5149d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135107975 | |||||
| chr2:135107975
|
CAAA | C | 22 | a0001c0001t0002g0139a0001c0001t0002g0158a0001c0001t0002g0160others(19): Show | 22 | HG00438.hp1 HG01070.hp1 HG02056.hp2 others(19): Show |
intron_variant | MODIFIER | c.363-5151_363-5149d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135107975 | |||||
| chr2:135107975
|
CAAAA | C | 81 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0140others(78): Show | 81 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(78): Show |
intron_variant | MODIFIER | c.363-5152_363-5149d others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135107975 | |||||
| chr2:135107975
|
CAAAAA | C | 46 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(43): Show | 46 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.363-5153_363-5149d others(7): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135107975 | |||||
| chr2:135108002
|
A | C | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.363-5149A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135108002 | ||||||
| chr2:135108457
|
C | T | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.363-4694C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135108457 | ||||||
| chr2:135108515
|
C | A | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.363-4636C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135108515 | ||||||
| chr2:135108515
|
C | CT | 38 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(35): Show | 38 | HG00438.hp1 HG01346.hp2 HG01975.hp2 others(35): Show |
intron_variant | MODIFIER | c.363-4622dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135108515 | |||||
| chr2:135108515
|
CT | C | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.363-4622delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135108515 | |||||
| chr2:135108592
|
C | G | 1 | a0002c0002t0001g0217 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.363-4559C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135108592 | ||||||
| chr2:135108612
|
G | A | 80 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(77): Show | 80 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.363-4539G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135108612 | ||||||
| chr2:135108812
|
C | T | 1 | a0002c0002t0001g0017 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.363-4339C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135108812 | ||||||
| chr2:135108985
|
A | G | 5 | a0001c0001t0001g0082a0004c0005t0011g0219a0004c0005t0011g0220others(2): Show | 5 | HG02055.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.363-4166A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135108985 | ||||||
| chr2:135109036
|
AT | A | 3 | a0001c0001t0002g0204a0001c0001t0002g0211a0001c0001t0010g0209 | 3 | HG03017.hp2 HG03654.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.363-4112delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135109036 | |||||
| chr2:135109143
|
TTGG | T | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.363-4007_363-4005d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109143 | ||||||
| chr2:135109180
|
A | G | 57 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(54): Show | 57 | HG00438.hp1 HG00741.hp2 HG01256.hp2 others(54): Show |
intron_variant | MODIFIER | c.363-3971A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109180 | ||||||
| chr2:135109209
|
C | T | 1 | a0002c0002t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.363-3942C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109209 | ||||||
| chr2:135109241
|
A | C | 1 | a0001c0001t0002g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.363-3910A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109241 | ||||||
| chr2:135109275
|
A | G | 2 | a0001c0001t0001g0032a0001c0001t0001g0071 | 2 | HG01255.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.363-3876A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109275 | ||||||
| chr2:135109513
|
C | T | 7 | a0001c0001t0004g0260a0001c0001t0004g0261a0001c0001t0004g0262others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.363-3638C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109513 | ||||||
| chr2:135109529
|
A | G | 4 | a0001c0001t0001g0040a0001c0001t0001g0073a0001c0001t0001g0218others(1): Show | 4 | HG00423.hp1 NA18968.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.363-3622A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109529 | ||||||
| chr2:135109574
|
T | A | 4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.363-3577T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109574 | ||||||
| chr2:135109587
|
T | A | 18 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(15): Show | 18 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.363-3564T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109587 | ||||||
| chr2:135109776
|
G | C | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363-3375G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109776 | ||||||
| chr2:135109803
|
C | T | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.363-3348C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109803 | ||||||
| chr2:135109841
|
C | T | 1 | a0002c0002t0001g0133 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.363-3310C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109841 | ||||||
| chr2:135109878
|
G | A | 1 | a0001c0001t0004g0267 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.363-3273G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109878 | ||||||
| chr2:135109932
|
A | G | 2 | a0001c0001t0002g0181a0001c0001t0002g0182 | 2 | HG01070.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.363-3219A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109932 | ||||||
| chr2:135109968
|
T | C | 4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.363-3183T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109968 | ||||||
| chr2:135109993
|
T | G | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.363-3158T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135109993 | ||||||
| chr2:135110063
|
A | G | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.363-3088A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135110063 | ||||||
| chr2:135110204
|
G | T | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.363-2947G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135110204 | ||||||
| chr2:135110340
|
G | C | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.363-2811G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135110340 | ||||||
| chr2:135110448
|
AAGAATTT others(6): Show |
A | 1 | a0001c0001t0004g0268 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.363-2701_363-2689d others(15): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135110448 | |||||
| chr2:135110729
|
C | T | 3 | a0001c0001t0012g0252a0001c0001t0012g0253a0001c0001t0012g0254 | 3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.363-2422C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135110729 | ||||||
| chr2:135110975
|
GA | G | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.363-2169delA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135110975 | |||||
| chr2:135111554
|
T | C | 1 | a0002c0002t0001g0100 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.363-1597T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135111554 | ||||||
| chr2:135111560
|
G | A | 1 | a0001c0001t0005g0007 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.363-1591G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135111560 | ||||||
| chr2:135111675
|
A | G | 1 | a0001c0001t0002g0184 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.363-1476A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135111675 | ||||||
| chr2:135111810
|
G | A | 41 | a0001c0001t0002g0247a0001c0001t0003g0227a0001c0001t0003g0228others(38): Show | 41 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.363-1341G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135111810 | ||||||
| chr2:135112003
|
G | A | 1 | a0001c0008t0008g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.363-1148G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112003 | ||||||
| chr2:135112020
|
G | C | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.363-1131G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112020 | ||||||
| chr2:135112106
|
G | A | 1 | a0002c0002t0001g0069 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.363-1045G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112106 | ||||||
| chr2:135112166
|
C | T | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.363-985C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112166 | ||||||
| chr2:135112191
|
C | T | 41 | a0001c0001t0002g0247a0001c0001t0003g0227a0001c0001t0003g0228others(38): Show | 41 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.363-960C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112191 | ||||||
| chr2:135112269
|
G | A | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.363-882G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112269 | ||||||
| chr2:135112427
|
A | G | 1 | a0001c0001t0003g0276 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.363-724A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112427 | ||||||
| chr2:135112573
|
C | A | 1 | a0002c0002t0001g0094 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.363-578C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112573 | ||||||
| chr2:135112625
|
G | A | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.363-526G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112625 | ||||||
| chr2:135112746
|
C | G | 10 | a0001c0001t0003g0234a0001c0001t0003g0235a0001c0001t0003g0236others(7): Show | 10 | HG01175.hp2 HG01884.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.363-405C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112746 | ||||||
| chr2:135112815
|
G | GTC | 4 | a0001c0001t0001g0040a0001c0001t0012g0252a0001c0001t0012g0253others(1): Show | 4 | HG02809.hp2 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.363-317_363-316dup others(2): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135112815 | |||||
| chr2:135112815
|
GTCTCTCT others(1): Show |
G | 5 | a0001c0001t0003g0277a0001c0001t0003g0279a0001c0004t0013g0246others(2): Show | 5 | HG02559.hp1 HG03041.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.363-323_363-316del others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135112815 | |||||
| chr2:135112824
|
TCTCTCTC others(5): Show |
T | 24 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(21): Show | 24 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.363-325_363-314del others(12): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135112824 | |||||
| chr2:135112826
|
TCTCTCTC others(3): Show |
T | 1 | a0001c0001t0003g0245 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.363-323_363-314del others(10): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135112826 | |||||
| chr2:135112828
|
T | A | 1 | a0001c0001t0003g0276 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.363-323T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112828 | ||||||
| chr2:135112830
|
T | A | 1 | a0001c0001t0003g0276 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.363-321T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112830 | ||||||
| chr2:135112830
|
TCTCTCA | T | 6 | a0001c0001t0001g0130a0001c0001t0001g0131a0003c0006t0002g0248others(3): Show | 6 | HG02258.hp2 HG02630.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.363-319_363-314del others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135112830 | |||||
| chr2:135112830
|
TCTCTCAC others(1): Show |
T | 5 | a0001c0001t0002g0247a0004c0005t0011g0219a0004c0005t0011g0220others(2): Show | 5 | HG01243.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.363-319_363-312del others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135112830 | |||||
| chr2:135112832
|
T | A | 1 | a0001c0001t0003g0276 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.363-319T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112832 | ||||||
| chr2:135112834
|
T | A | 2 | a0001c0001t0003g0276a0001c0004t0013g0256 | 2 | HG00639.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.363-317T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112834 | ||||||
| chr2:135112834
|
T | TCA | 14 | a0001c0001t0002g0161a0001c0001t0002g0199a0001c0001t0002g0205others(11): Show | 14 | HG01071.hp1 HG01175.hp1 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.363-284_363-283dup others(2): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135112834 | |||||
| chr2:135112834
|
T | TCACA | 55 | a0001c0001t0002g0002a0001c0001t0002g0139a0001c0001t0002g0140others(52): Show | 55 | HG00438.hp1 HG01070.hp1 HG01192.hp1 others(52): Show |
intron_variant | MODIFIER | c.363-286_363-283dup others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135112834 | |||||
| chr2:135112834
|
T | TCACACA | 6 | a0001c0001t0001g0159a0001c0001t0002g0146a0001c0001t0002g0160others(3): Show | 6 | HG02015.hp2 HG02451.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.363-288_363-283dup others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135112834 | |||||
| chr2:135112834
|
T | TCACACAC others(1): Show |
3 | a0001c0001t0002g0163a0001c0001t0002g0173a0001c0001t0002g0216 | 3 | HG02083.hp2 HG04115.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.363-290_363-283dup others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135112834 | |||||
| chr2:135112834
|
T | TCTCA | 9 | a0001c0001t0002g0147a0001c0001t0002g0150a0001c0001t0002g0151others(6): Show | 9 | HG00741.hp2 HG01256.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.363-316_363-315ins others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135112834 | |||||
| chr2:135112834
|
TCACA | T | 6 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0081others(3): Show | 6 | HG00735.hp1 HG01358.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.363-286_363-283del others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135112834 | |||||
| chr2:135112834
|
TCACACAC others(1): Show |
T | 12 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(9): Show | 12 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.363-290_363-283del others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 135112834 | |||||
| chr2:135112836
|
A | T | 19 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0004g0258others(16): Show | 19 | HG02055.hp1 HG02056.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.363-315A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112836 | ||||||
| chr2:135112838
|
A | T | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.363-313A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112838 | ||||||
| chr2:135112842
|
A | T | 2 | a0001c0008t0008g0005a0001c0008t0008g0006 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.363-309A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112842 | ||||||
| chr2:135112844
|
A | T | 13 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(10): Show | 13 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.363-307A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112844 | ||||||
| chr2:135112877
|
C | T | 1 | a0002c0002t0001g0113 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.363-274C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112877 | ||||||
| chr2:135112971
|
A | G | 1 | a0002c0002t0001g0033 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.363-180A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 5/23 | chr2 | 135112971 | ||||||
| chr2:135113392
|
T | A | 2 | a0002c0002t0001g0101a0002c0002t0001g0217 | 2 | HG02083.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.482+122T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135113392 | ||||||
| chr2:135113418
|
C | T | 3 | a0001c0001t0003g0276a0001c0001t0003g0277a0001c0001t0003g0279 | 3 | HG00639.hp1 HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.482+148C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135113418 | ||||||
| chr2:135113494
|
A | G | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.482+224A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135113494 | ||||||
| chr2:135113568
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.482+298C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135113568 | ||||||
| chr2:135113742
|
AT | A | 6 | a0001c0001t0002g0189a0001c0001t0002g0190a0003c0006t0002g0248others(3): Show | 6 | HG02258.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.482+486delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 135113742 | |||||
| chr2:135113864
|
C | T | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.482+594C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135113864 | ||||||
| chr2:135113992
|
C | T | 1 | a0001c0001t0002g0213 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.482+722C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135113992 | ||||||
| chr2:135114001
|
C | T | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.482+731C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135114001 | ||||||
| chr2:135114054
|
G | A | 150 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(147): Show | 150 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(147): Show |
intron_variant | MODIFIER | c.482+784G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135114054 | ||||||
| chr2:135114344
|
C | T | 99 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(96): Show | 99 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(96): Show |
intron_variant | MODIFIER | c.483-872C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135114344 | ||||||
| chr2:135114418
|
A | G | 2 | a0001c0001t0015g0272a0001c0001t0015g0273 | 2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.483-798A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135114418 | ||||||
| chr2:135114528
|
C | T | 3 | a0001c0001t0012g0252a0001c0001t0012g0253a0001c0001t0012g0254 | 3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.483-688C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135114528 | ||||||
| chr2:135114576
|
G | T | 24 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(21): Show | 24 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.483-640G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135114576 | ||||||
| chr2:135114805
|
G | A | 1 | a0001c0001t0004g0268 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.483-411G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135114805 | ||||||
| chr2:135115072
|
T | A | 1 | a0001c0001t0003g0277 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.483-144T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135115072 | ||||||
| chr2:135115076
|
C | A | 151 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(148): Show | 151 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.483-140C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135115076 | ||||||
| chr2:135115153
|
T | G | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.483-63T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 6/23 | chr2 | 135115153 | ||||||
| chr2:135115896
|
A | G | 2 | a0001c0003t0001g0042a0001c0003t0001g0085 | 2 | HG02258.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.648+515A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135115896 | ||||||
| chr2:135116015
|
G | A | 1 | a0001c0001t0003g0279 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.648+634G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135116015 | ||||||
| chr2:135116162
|
T | G | 1 | a0001c0001t0003g0277 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.648+781T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135116162 | ||||||
| chr2:135116272
|
T | A | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.648+891T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135116272 | ||||||
| chr2:135116275
|
C | T | 51 | a0001c0001t0002g0247a0001c0001t0003g0227a0001c0001t0003g0228others(48): Show | 51 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.648+894C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135116275 | ||||||
| chr2:135116387
|
C | T | 2 | a0002c0002t0001g0126a0002c0002t0001g0127 | 2 | HG01192.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.648+1006C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135116387 | ||||||
| chr2:135116402
|
T | C | 1 | a0001c0003t0001g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.648+1021T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135116402 | ||||||
| chr2:135116468
|
C | T | 154 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(151): Show | 154 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.648+1087C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135116468 | ||||||
| chr2:135116470
|
G | T | 1 | a0005c0014t0002g0202 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.648+1089G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135116470 | ||||||
| chr2:135116656
|
A | G | 1 | a0002c0002t0001g0217 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.648+1275A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135116656 | ||||||
| chr2:135117036
|
T | C | 4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.648+1655T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117036 | ||||||
| chr2:135117052
|
A | G | 151 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(148): Show | 151 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.648+1671A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117052 | ||||||
| chr2:135117057
|
G | C | 5 | a0001c0001t0003g0234a0001c0001t0003g0237a0001c0001t0003g0240others(2): Show | 5 | HG01175.hp2 HG02109.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.648+1676G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117057 | ||||||
| chr2:135117195
|
G | A | 4 | a0001c0001t0003g0245a0001c0001t0003g0276a0001c0001t0003g0277others(1): Show | 4 | HG00639.hp1 HG01261.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.648+1814G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117195 | ||||||
| chr2:135117409
|
T | TTCTTCTT others(13): Show |
1 | a0001c0001t0006g0239 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.648+2029_648+2030i others(22): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117409 | |||||
| chr2:135117409
|
T | TTTC | 14 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0067others(11): Show | 14 | HG00280.hp2 HG00609.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.648+2072_648+2074d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117409 | |||||
| chr2:135117409
|
T | TTTCTTC | 26 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0046others(23): Show | 27 | HG00609.hp2 HG01175.hp1 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.648+2069_648+2074d others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117409 | |||||
| chr2:135117409
|
T | TTTCTTCT others(2): Show |
26 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0049others(23): Show | 26 | HG00621.hp2 HG01243.hp1 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.648+2066_648+2074d others(11): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117409 | |||||
| chr2:135117409
|
T | TTTCTTCT others(5): Show |
31 | a0001c0001t0001g0032a0001c0001t0001g0084a0001c0001t0001g0218others(28): Show | 31 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.648+2063_648+2074d others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117409 | |||||
| chr2:135117409
|
T | TTTCTTCT others(8): Show |
27 | a0001c0001t0001g0048a0001c0001t0001g0051a0001c0001t0001g0065others(24): Show | 27 | HG00438.hp2 HG00558.hp2 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.648+2060_648+2074d others(17): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117409 | |||||
| chr2:135117409
|
T | TTTCTTCT others(11): Show |
13 | a0001c0001t0001g0044a0001c0001t0001g0073a0001c0001t0001g0214others(10): Show | 13 | HG00423.hp1 HG00735.hp2 HG02896.hp2 others(10): Show |
intron_variant | MODIFIER | c.648+2057_648+2074d others(20): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117409 | |||||
| chr2:135117409
|
T | TTTCTTCT others(14): Show |
12 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0090others(9): Show | 12 | HG01255.hp1 HG01261.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.648+2054_648+2074d others(23): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117409 | |||||
| chr2:135117409
|
T | TTTCTTCT others(20): Show |
1 | a0001c0001t0003g0240 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.648+2048_648+2074d others(29): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117409 | |||||
| chr2:135117409
|
TTTC | T | 5 | a0001c0001t0001g0031a0001c0001t0001g0037a0001c0001t0001g0102others(2): Show | 5 | HG02809.hp1 HG02886.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.648+2072_648+2074d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117409 | |||||
| chr2:135117432
|
TCTTCTTC others(17): Show |
T | 1 | a0001c0001t0010g0179 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.648+2057_648+2080d others(26): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117432 | |||||
| chr2:135117435
|
TCTTCTTC others(14): Show |
T | 4 | a0001c0001t0002g0147a0001c0001t0002g0150a0001c0001t0002g0151others(1): Show | 4 | HG00741.hp2 HG01256.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.648+2060_648+2080d others(23): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117435 | |||||
| chr2:135117438
|
TCTTCTTC others(11): Show |
T | 4 | a0001c0001t0002g0163a0001c0001t0002g0164a0001c0001t0022g0175others(1): Show | 4 | HG03688.hp2 HG03942.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.648+2063_648+2080d others(20): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117438 | |||||
| chr2:135117441
|
TCTTCTTC others(8): Show |
T | 58 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(55): Show | 58 | HG00438.hp1 HG01070.hp1 HG01192.hp1 others(55): Show |
intron_variant | MODIFIER | c.648+2066_648+2080d others(17): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117441 | |||||
| chr2:135117444
|
TCTTCTTC others(5): Show |
T | 9 | a0001c0001t0002g0143a0001c0001t0002g0149a0001c0001t0002g0155others(6): Show | 9 | HG01978.hp2 HG03017.hp2 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.648+2069_648+2080d others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117444 | |||||
| chr2:135117450
|
T | G | 4 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0002g0189others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.648+2069T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117450 | ||||||
| chr2:135117450
|
T | TCTTCTTC others(11): Show |
1 | a0002c0002t0001g0086 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.648+2074_648+2075i others(20): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117450 | |||||
| chr2:135117450
|
TCTTCTG | T | 3 | a0001c0001t0002g0161a0001c0001t0003g0277a0001c0004t0013g0246 | 3 | HG02818.hp2 HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.648+2093_648+2098d others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117450 | |||||
| chr2:135117456
|
G | T | 42 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0045others(39): Show | 42 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.648+2075G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117456 | ||||||
| chr2:135117462
|
G | T | 37 | a0001c0001t0002g0247a0001c0001t0003g0227a0001c0001t0003g0230others(34): Show | 37 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.648+2081G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117462 | ||||||
| chr2:135117468
|
G | T | 2 | a0001c0001t0003g0232a0001c0001t0017g0224 | 2 | HG00621.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.648+2087G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117468 | ||||||
| chr2:135117474
|
G | T | 5 | a0001c0001t0003g0232a0001c0001t0017g0224a0004c0005t0011g0219others(2): Show | 5 | HG00621.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.648+2093G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117474 | ||||||
| chr2:135117477
|
T | G | 3 | a0004c0005t0011g0219a0004c0005t0011g0222a0004c0005t0025g0221 | 3 | HG02895.hp1 HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.648+2096T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117477 | ||||||
| chr2:135117483
|
G | T | 7 | a0001c0001t0001g0045a0001c0001t0002g0189a0001c0001t0002g0190others(4): Show | 7 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.648+2102G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117483 | ||||||
| chr2:135117486
|
T | G | 3 | a0001c0001t0001g0045a0001c0001t0002g0189a0001c0001t0002g0190 | 3 | HG02896.hp1 HG02897.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.648+2105T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117486 | ||||||
| chr2:135117489
|
T | G | 3 | a0004c0005t0011g0219a0004c0005t0011g0222a0004c0005t0025g0221 | 3 | HG02895.hp1 HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.648+2108T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117489 | ||||||
| chr2:135117492
|
T | G | 1 | a0002c0002t0001g0129 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.648+2111T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117492 | ||||||
| chr2:135117495
|
G | T | 7 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0003g0232others(4): Show | 7 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.648+2114G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117495 | ||||||
| chr2:135117495
|
GCTT | G | 17 | a0001c0001t0002g0161a0001c0001t0002g0188a0001c0001t0005g0007others(14): Show | 17 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.648+2129_648+2131d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117495 | |||||
| chr2:135117504
|
T | G | 6 | a0001c0001t0002g0189a0001c0001t0002g0190a0002c0002t0001g0129others(3): Show | 6 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.648+2123T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117504 | ||||||
| chr2:135117504
|
T | TCTTCTTC others(23): Show |
1 | a0001c0001t0003g0232 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.648+2137_648+2138i others(32): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117504 | |||||
| chr2:135117510
|
T | G | 22 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(19): Show | 22 | HG00558.hp1 HG00639.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.648+2129T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117510 | ||||||
| chr2:135117513
|
G | T | 23 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(20): Show | 23 | HG00558.hp1 HG00639.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.648+2132G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117513 | ||||||
| chr2:135117519
|
T | G | 22 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(19): Show | 22 | HG00558.hp1 HG00639.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.648+2138T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117519 | ||||||
| chr2:135117522
|
G | GCTT | 10 | a0001c0001t0003g0232a0001c0001t0003g0245a0001c0001t0003g0276others(7): Show | 10 | HG00621.hp1 HG00639.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.648+2147_648+2149d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117522 | |||||
| chr2:135117522
|
G | T | 22 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(19): Show | 22 | HG00558.hp1 HG00639.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.648+2141G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117522 | ||||||
| chr2:135117522
|
GCTT | G | 11 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0207others(8): Show | 11 | HG03017.hp2 HG03654.hp1 HG03704.hp1 others(8): Show |
intron_variant | MODIFIER | c.648+2147_648+2149d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117522 | |||||
| chr2:135117531
|
G | T | 3 | a0001c0001t0002g0185a0001c0001t0002g0189a0001c0001t0002g0190 | 3 | HG02896.hp1 HG02897.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.648+2150G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117531 | ||||||
| chr2:135117531
|
GCTTCTTC others(8): Show |
G | 2 | a0001c0001t0002g0164a0001c0001t0002g0199 | 2 | HG04228.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.648+2174_648+2188d others(17): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117531 | |||||
| chr2:135117534
|
T | G | 3 | a0001c0001t0002g0185a0001c0001t0002g0189a0001c0001t0002g0190 | 3 | HG02896.hp1 HG02897.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.648+2153T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117534 | ||||||
| chr2:135117543
|
G | T | 3 | a0001c0001t0002g0185a0001c0001t0002g0189a0001c0001t0002g0190 | 3 | HG02896.hp1 HG02897.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.648+2162G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117543 | ||||||
| chr2:135117543
|
GCTT | G | 75 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(72): Show | 75 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(72): Show |
intron_variant | MODIFIER | c.648+2174_648+2176d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117543 | |||||
| chr2:135117546
|
T | G | 35 | a0001c0001t0002g0185a0001c0001t0002g0189a0001c0001t0002g0190others(32): Show | 35 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.648+2165T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117546 | ||||||
| chr2:135117546
|
T | TCTTCTTC others(5): Show |
4 | a0003c0006t0002g0248a0003c0006t0009g0249a0003c0006t0009g0250others(1): Show | 4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.648+2173_648+2174i others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117546 | |||||
| chr2:135117546
|
T | TCTTCTTC others(5): Show |
5 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0012g0252others(2): Show | 5 | HG02809.hp2 HG03130.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.648+2204_648+2215d others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117546 | |||||
| chr2:135117546
|
TCTTCTTC others(5): Show |
T | 10 | a0001c0001t0001g0039a0002c0002t0001g0033a0002c0002t0001g0075others(7): Show | 10 | HG01175.hp1 HG01255.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.648+2204_648+2215d others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117546 | |||||
| chr2:135117555
|
T | G | 5 | a0001c0001t0002g0247a0001c0004t0013g0246a0001c0004t0013g0256others(2): Show | 5 | HG01243.hp1 HG03130.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.648+2174T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117555 | ||||||
| chr2:135117561
|
T | TCTTCTTC others(2): Show |
4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.648+2189_648+2197d others(11): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117561 | |||||
| chr2:135117573
|
TCTTCTTC others(2): Show |
T | 3 | a0001c0001t0002g0146a0001c0001t0002g0149a0001c0001t0002g0185 | 3 | HG03834.hp2 NA18969.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.648+2201_648+2209d others(11): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117573 | |||||
| chr2:135117579
|
T | G | 36 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0143others(33): Show | 36 | HG00438.hp1 HG01346.hp2 HG01978.hp2 others(33): Show |
intron_variant | MODIFIER | c.648+2198T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117579 | ||||||
| chr2:135117579
|
T | TCTG | 4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.648+2201_648+2203d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117579 | |||||
| chr2:135117582
|
G | GCTT | 68 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0142others(65): Show | 68 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.648+2210_648+2212d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117582 | |||||
| chr2:135117582
|
G | GCTTCTTC others(5): Show |
2 | a0001c0001t0002g0139a0001c0001t0002g0171 | 2 | HG02056.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.648+2209_648+2210i others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117582 | |||||
| chr2:135117582
|
G | GCTTCTTC others(8): Show |
27 | a0001c0001t0002g0247a0001c0001t0004g0258a0001c0001t0004g0259others(24): Show | 27 | HG00280.hp1 HG01243.hp1 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.648+2215_648+2216i others(17): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117582 | |||||
| chr2:135117582
|
G | T | 36 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0143others(33): Show | 36 | HG00438.hp1 HG01346.hp2 HG01978.hp2 others(33): Show |
intron_variant | MODIFIER | c.648+2201G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117582 | ||||||
| chr2:135117594
|
G | GCTTCTTC others(47): Show |
1 | a0001c0008t0008g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.648+2215_648+2216i others(56): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117594 | |||||
| chr2:135117603
|
T | G | 1 | a0001c0001t0010g0180 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.648+2222T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117603 | ||||||
| chr2:135117606
|
G | T | 1 | a0001c0008t0008g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.648+2225G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117606 | ||||||
| chr2:135117609
|
T | G | 1 | a0001c0008t0008g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.648+2228T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117609 | ||||||
| chr2:135117639
|
T | G | 1 | a0001c0001t0002g0148 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.648+2258T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117639 | ||||||
| chr2:135117639
|
T | TCTTCTTC others(8): Show |
1 | a0002c0002t0001g0115 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.648+2297_648+2311d others(17): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117639 | |||||
| chr2:135117645
|
T | G | 1 | a0001c0008t0008g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.648+2264T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117645 | ||||||
| chr2:135117648
|
G | T | 1 | a0001c0008t0008g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.648+2267G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117648 | ||||||
| chr2:135117654
|
G | T | 1 | a0001c0001t0003g0232 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.648+2273G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117654 | ||||||
| chr2:135117657
|
T | TCTGCTTC others(5): Show |
13 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(10): Show | 13 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.648+2278_648+2279i others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117657 | |||||
| chr2:135117660
|
T | G | 1 | a0001c0008t0008g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.648+2279T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117660 | ||||||
| chr2:135117663
|
G | GCTT | 13 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(10): Show | 13 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.648+2285_648+2287d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117663 | |||||
| chr2:135117663
|
G | GCTTCTGC others(2): Show |
30 | a0001c0001t0002g0247a0001c0001t0003g0227a0001c0001t0003g0228others(27): Show | 30 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.648+2294_648+2302d others(11): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117663 | |||||
| chr2:135117663
|
G | GCTTCTGC others(11): Show |
4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.648+2285_648+2302d others(20): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117663 | |||||
| chr2:135117663
|
G | T | 1 | a0001c0008t0008g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.648+2282G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117663 | ||||||
| chr2:135117681
|
TCTG | T | 3 | a0003c0006t0009g0249a0003c0006t0009g0250a0003c0006t0009g0251 | 3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.648+2303_648+2305d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117681 | |||||
| chr2:135117684
|
G | T | 3 | a0001c0001t0003g0276a0001c0001t0003g0279a0003c0006t0002g0248 | 3 | HG00639.hp1 HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.648+2303G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117684 | ||||||
| chr2:135117687
|
T | G | 3 | a0001c0001t0003g0276a0001c0001t0003g0279a0003c0006t0002g0248 | 3 | HG00639.hp1 HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.648+2306T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117687 | ||||||
| chr2:135117690
|
T | G | 3 | a0003c0006t0009g0249a0003c0006t0009g0250a0003c0006t0009g0251 | 3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.648+2309T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117690 | ||||||
| chr2:135117693
|
T | G | 3 | a0001c0001t0003g0276a0001c0001t0003g0279a0003c0006t0002g0248 | 3 | HG00639.hp1 HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.648+2312T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117693 | ||||||
| chr2:135117696
|
G | T | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.648+2315G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117696 | ||||||
| chr2:135117702
|
TCTG | T | 3 | a0003c0006t0009g0249a0003c0006t0009g0250a0003c0006t0009g0251 | 3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.648+2324_648+2326d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117702 | |||||
| chr2:135117711
|
G | T | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.648+2330G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117711 | ||||||
| chr2:135117714
|
T | G | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.648+2333T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117714 | ||||||
| chr2:135117720
|
T | G | 3 | a0003c0006t0009g0249a0003c0006t0009g0250a0003c0006t0009g0251 | 3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.648+2339T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117720 | ||||||
| chr2:135117723
|
G | T | 3 | a0003c0006t0009g0249a0003c0006t0009g0250a0003c0006t0009g0251 | 3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.648+2342G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117723 | ||||||
| chr2:135117726
|
T | G | 3 | a0003c0006t0009g0249a0003c0006t0009g0250a0003c0006t0009g0251 | 3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.648+2345T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117726 | ||||||
| chr2:135117729
|
T | G | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.648+2348T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117729 | ||||||
| chr2:135117738
|
GCTT | G | 4 | a0003c0006t0002g0248a0003c0006t0009g0249a0003c0006t0009g0250others(1): Show | 4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.648+2366_648+2368d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117738 | |||||
| chr2:135117784
|
C | T | 1 | a0001c0001t0003g0279 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.648+2403C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117784 | ||||||
| chr2:135117786
|
G | T | 3 | a0001c0001t0004g0266a0002c0002t0001g0001a0002c0002t0001g0134 | 4 | HG03540.hp2 NA18952.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.648+2405G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117786 | ||||||
| chr2:135117789
|
T | G | 1 | a0001c0001t0001g0051 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.648+2408T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117789 | ||||||
| chr2:135117793
|
C | CTTCTTCT others(19): Show |
4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.648+2427_648+2452d others(28): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117793 | |||||
| chr2:135117795
|
T | C | 1 | a0001c0004t0013g0256 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.648+2414T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135117795 | ||||||
| chr2:135117799
|
CTTCTTCT others(3): Show |
C | 2 | a0001c0004t0013g0257a0001c0004t0026g0255 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.648+2440_648+2449d others(12): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117799 | |||||
| chr2:135117800
|
TTCTTCTT others(15): Show |
T | 1 | a0001c0001t0004g0266 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.648+2421_648+2442d others(24): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117800 | |||||
| chr2:135117803
|
TTCTTCTT others(12): Show |
T | 1 | a0001c0001t0003g0277 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.648+2424_648+2442d others(21): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117803 | |||||
| chr2:135117809
|
TTTCTTCT others(6): Show |
T | 36 | a0001c0001t0002g0185a0001c0001t0002g0187a0001c0001t0002g0247others(33): Show | 36 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.648+2466_648+2478d others(15): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117809 | |||||
| chr2:135117832
|
T | TTTC | 3 | a0003c0006t0009g0249a0003c0006t0009g0250a0003c0006t0009g0251 | 3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.648+2463_648+2465d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135117832 | |||||
| chr2:135118044
|
G | T | 1 | a0008c0012t0008g0003 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.648+2663G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135118044 | ||||||
| chr2:135118088
|
C | T | 1 | a0001c0001t0012g0254 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.648+2707C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135118088 | ||||||
| chr2:135118278
|
TA | T | 16 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0142others(13): Show | 16 | HG00741.hp2 HG01256.hp2 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.649-2531delA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135118278 | |||||
| chr2:135118304
|
A | G | 4 | a0003c0006t0002g0248a0003c0006t0009g0249a0003c0006t0009g0250others(1): Show | 4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.649-2515A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135118304 | ||||||
| chr2:135118353
|
T | C | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.649-2466T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135118353 | ||||||
| chr2:135118413
|
C | G | 1 | a0001c0001t0022g0175 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.649-2406C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135118413 | ||||||
| chr2:135118550
|
T | A | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.649-2269T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135118550 | ||||||
| chr2:135118621
|
T | A | 1 | a0001c0001t0003g0276 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.649-2198T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135118621 | ||||||
| chr2:135118738
|
C | T | 80 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(77): Show | 80 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.649-2081C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135118738 | ||||||
| chr2:135118888
|
T | TC | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.649-1928dupC | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135118888 | |||||
| chr2:135119047
|
T | C | 1 | a0001c0001t0003g0234 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.649-1772T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135119047 | ||||||
| chr2:135119070
|
T | TCCTC | 25 | a0001c0001t0001g0084a0001c0001t0003g0227a0001c0001t0003g0228others(22): Show | 25 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.649-1725_649-1722d others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135119070 | |||||
| chr2:135119070
|
TCCTC | T | 101 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(98): Show | 101 | HG00280.hp1 HG00438.hp1 HG00741.hp2 others(98): Show |
intron_variant | MODIFIER | c.649-1725_649-1722d others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135119070 | |||||
| chr2:135119070
|
TCCTCCCT others(5): Show |
T | 1 | a0001c0001t0003g0237 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.649-1733_649-1722d others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135119070 | |||||
| chr2:135119094
|
C | T | 3 | a0003c0006t0009g0249a0003c0006t0009g0250a0003c0006t0009g0251 | 3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.649-1725C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135119094 | ||||||
| chr2:135119357
|
G | A | 1 | a0002c0002t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.649-1462G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135119357 | ||||||
| chr2:135119419
|
T | C | 1 | a0004c0005t0011g0220 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.649-1400T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135119419 | ||||||
| chr2:135119559
|
A | C | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.649-1260A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135119559 | ||||||
| chr2:135119563
|
G | T | 1 | a0001c0001t0002g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.649-1256G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135119563 | ||||||
| chr2:135119578
|
C | CA | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.649-1237dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135119578 | |||||
| chr2:135119992
|
A | G | 224 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0078others(221): Show | 225 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(222): Show |
intron_variant | MODIFIER | c.649-827A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135119992 | ||||||
| chr2:135120126
|
C | T | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.649-693C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135120126 | ||||||
| chr2:135120504
|
G | A | 2 | a0004c0005t0011g0219a0004c0005t0011g0222 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.649-315G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135120504 | ||||||
| chr2:135120682
|
T | C | 5 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0081others(2): Show | 5 | HG00735.hp1 HG01358.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.649-137T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135120682 | ||||||
| chr2:135120703
|
TC | T | 5 | a0002c0002t0001g0001a0002c0002t0001g0097a0002c0002t0001g0109others(2): Show | 6 | HG00609.hp2 NA18942.hp2 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.649-114delC | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 135120703 | |||||
| chr2:135120737
|
A | G | 1 | a0001c0001t0010g0179 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.649-82A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 7/23 | chr2 | 135120737 | ||||||
| chr2:135121244
|
G | A | 153 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(150): Show | 153 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.748+326G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135121244 | ||||||
| chr2:135121331
|
G | C | 1 | a0001c0001t0015g0273 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.748+413G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135121331 | ||||||
| chr2:135121450
|
T | C | 1 | a0002c0002t0001g0121 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.748+532T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135121450 | ||||||
| chr2:135121647
|
A | G | 3 | a0001c0001t0001g0039a0001c0001t0001g0066a0001c0001t0001g0132 | 3 | HG02074.hp2 HG02129.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.748+729A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135121647 | ||||||
| chr2:135121682
|
C | G | 1 | a0002c0002t0001g0125 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.748+764C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135121682 | ||||||
| chr2:135121688
|
C | T | 2 | a0002c0002t0001g0075a0002c0002t0001g0083 | 2 | HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.748+770C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135121688 | ||||||
| chr2:135121908
|
C | T | 3 | a0001c0004t0013g0256a0001c0004t0013g0257a0001c0004t0026g0255 | 3 | HG03130.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.748+990C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135121908 | ||||||
| chr2:135121912
|
GT | G | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.748+995delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135121912 | ||||||
| chr2:135122049
|
C | T | 3 | a0001c0007t0002g0018a0001c0007t0002g0019a0001c0007t0002g0020 | 3 | HG02280.hp2 HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.748+1131C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135122049 | ||||||
| chr2:135122083
|
A | G | 3 | a0001c0004t0013g0256a0001c0004t0013g0257a0001c0004t0026g0255 | 3 | HG03130.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.748+1165A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135122083 | ||||||
| chr2:135122092
|
C | CA | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.748+1184dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr2 | 135122092 | |||||
| chr2:135122379
|
TC | T | 55 | a0001c0001t0002g0247a0001c0001t0003g0227a0001c0001t0003g0228others(52): Show | 55 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.748+1463delC | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr2 | 135122379 | |||||
| chr2:135122443
|
G | A | 151 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(148): Show | 151 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.748+1525G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135122443 | ||||||
| chr2:135122495
|
A | G | 9 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0081others(6): Show | 9 | HG00735.hp1 HG01358.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.748+1577A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135122495 | ||||||
| chr2:135122611
|
G | T | 1 | a0001c0001t0002g0185 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.749-1554G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135122611 | ||||||
| chr2:135122917
|
T | C | 4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.749-1248T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135122917 | ||||||
| chr2:135123114
|
T | C | 1 | a0001c0001t0007g0145 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.749-1051T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135123114 | ||||||
| chr2:135123433
|
T | C | 1 | a0001c0001t0005g0009 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.749-732T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135123433 | ||||||
| chr2:135123624
|
C | A | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.749-541C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135123624 | ||||||
| chr2:135123907
|
A | G | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.749-258A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135123907 | ||||||
| chr2:135124086
|
T | C | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.749-79T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 8/23 | chr2 | 135124086 | ||||||
| chr2:135124382
|
C | T | 2 | a0002c0002t0001g0075a0002c0002t0001g0083 | 2 | HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.830+136C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 9/23 | chr2 | 135124382 | ||||||
| chr2:135124418
|
C | T | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.830+172C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 9/23 | chr2 | 135124418 | ||||||
| chr2:135124519
|
A | T | 4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.830+273A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 9/23 | chr2 | 135124519 | ||||||
| chr2:135124589
|
C | T | 24 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(21): Show | 24 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.830+343C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 9/23 | chr2 | 135124589 | ||||||
| chr2:135124774
|
A | G | 1 | a0001c0001t0002g0146 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.830+528A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 9/23 | chr2 | 135124774 | ||||||
| chr2:135124821
|
T | C | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.830+575T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 9/23 | chr2 | 135124821 | ||||||
| chr2:135124922
|
G | A | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.830+676G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 9/23 | chr2 | 135124922 | ||||||
| chr2:135125136
|
C | T | 2 | a0001c0001t0002g0149a0001c0001t0002g0193 | 2 | NA18979.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.830+890C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 9/23 | chr2 | 135125136 | ||||||
| chr2:135125383
|
T | C | 19 | a0001c0001t0002g0176a0001c0001t0003g0277a0001c0001t0003g0279others(16): Show | 19 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.831-798T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 9/23 | chr2 | 135125383 | ||||||
| chr2:135125898
|
G | A | 4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.831-283G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 9/23 | chr2 | 135125898 | ||||||
| chr2:135125976
|
A | G | 1 | a0001c0001t0001g0050 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.831-205A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 9/23 | chr2 | 135125976 | ||||||
| chr2:135126855
|
T | C | 1 | a0002c0002t0001g0098 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.973+199T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135126855 | ||||||
| chr2:135126917
|
G | C | 154 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(151): Show | 154 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.973+261G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135126917 | ||||||
| chr2:135127088
|
G | T | 1 | a0002c0002t0001g0127 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.973+432G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135127088 | ||||||
| chr2:135127090
|
T | G | 1 | a0001c0001t0012g0252 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.973+434T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135127090 | ||||||
| chr2:135127111
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.973+455G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135127111 | ||||||
| chr2:135127130
|
C | A | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.973+474C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135127130 | ||||||
| chr2:135127149
|
A | G | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.973+493A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135127149 | ||||||
| chr2:135127187
|
CT | C | 10 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0002g0146others(7): Show | 10 | HG01192.hp1 HG02293.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.973+547delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr2 | 135127187 | |||||
| chr2:135127329
|
T | TTTTG | 10 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(7): Show | 10 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.973+701_973+704dup others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr2 | 135127329 | |||||
| chr2:135127329
|
TTTTG | T | 9 | a0001c0001t0002g0176a0001c0001t0003g0233a0001c0001t0004g0268others(6): Show | 9 | HG02109.hp2 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.973+701_973+704del others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr2 | 135127329 | |||||
| chr2:135127422
|
T | C | 1 | a0001c0001t0002g0187 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.973+766T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135127422 | ||||||
| chr2:135127468
|
G | T | 3 | a0001c0001t0002g0163a0001c0001t0002g0164a0001c0001t0023g0201 | 3 | HG03942.hp2 HG04115.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.973+812G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135127468 | ||||||
| chr2:135127584
|
C | T | 1 | a0001c0001t0001g0218 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.973+928C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135127584 | ||||||
| chr2:135127628
|
C | T | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.973+972C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135127628 | ||||||
| chr2:135127787
|
C | T | 151 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(148): Show | 151 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.973+1131C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135127787 | ||||||
| chr2:135127873
|
T | A | 1 | a0001c0001t0005g0015 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.973+1217T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135127873 | ||||||
| chr2:135127881
|
A | G | 5 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0242others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.973+1225A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135127881 | ||||||
| chr2:135128013
|
A | G | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.973+1357A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135128013 | ||||||
| chr2:135128374
|
A | G | 3 | a0001c0001t0002g0161a0001c0001t0002g0189a0001c0001t0002g0190 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.974-1621A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135128374 | ||||||
| chr2:135128388
|
T | C | 1 | a0001c0001t0003g0276 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.974-1607T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135128388 | ||||||
| chr2:135128494
|
C | T | 3 | a0003c0006t0009g0249a0003c0006t0009g0250a0003c0006t0009g0251 | 3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.974-1501C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135128494 | ||||||
| chr2:135128627
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.974-1368A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135128627 | ||||||
| chr2:135128814
|
T | G | 1 | a0001c0001t0005g0015 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.974-1181T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135128814 | ||||||
| chr2:135128819
|
G | C | 1 | a0001c0001t0002g0149 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.974-1176G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135128819 | ||||||
| chr2:135128839
|
C | T | 8 | a0001c0001t0003g0227a0001c0001t0003g0244a0001c0001t0003g0275others(5): Show | 8 | HG00558.hp1 HG00621.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.974-1156C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135128839 | ||||||
| chr2:135128893
|
A | G | 1 | a0001c0001t0003g0245 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.974-1102A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135128893 | ||||||
| chr2:135128916
|
C | T | 41 | a0001c0001t0002g0247a0001c0001t0003g0227a0001c0001t0003g0228others(38): Show | 41 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.974-1079C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135128916 | ||||||
| chr2:135128941
|
G | A | 4 | a0003c0006t0002g0248a0003c0006t0009g0249a0003c0006t0009g0250others(1): Show | 4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.974-1054G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135128941 | ||||||
| chr2:135129131
|
G | A | 8 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(5): Show | 8 | HG01070.hp1 HG01192.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.974-864G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135129131 | ||||||
| chr2:135129174
|
C | T | 57 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(54): Show | 57 | HG00438.hp1 HG00741.hp2 HG01256.hp2 others(54): Show |
intron_variant | MODIFIER | c.974-821C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135129174 | ||||||
| chr2:135129175
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.974-820G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135129175 | ||||||
| chr2:135129178
|
C | T | 2 | a0002c0002t0001g0111a0002c0002t0001g0112 | 2 | NA20805.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.974-817C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135129178 | ||||||
| chr2:135129279
|
C | T | 15 | a0001c0001t0002g0147a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00280.hp1 HG00741.hp2 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.974-716C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135129279 | ||||||
| chr2:135129302
|
A | G | 1 | a0002c0002t0001g0098 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.974-693A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135129302 | ||||||
| chr2:135129363
|
A | G | 1 | a0001c0001t0003g0244 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.974-632A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135129363 | ||||||
| chr2:135129460
|
A | T | 14 | a0001c0001t0002g0216a0001c0001t0005g0007a0001c0001t0005g0008others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.974-535A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135129460 | ||||||
| chr2:135129487
|
T | C | 1 | a0006c0013t0005g0004 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.974-508T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135129487 | ||||||
| chr2:135129496
|
C | T | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.974-499C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135129496 | ||||||
| chr2:135129497
|
G | A | 2 | a0001c0001t0001g0032a0001c0001t0001g0071 | 2 | HG01255.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.974-498G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135129497 | ||||||
| chr2:135129635
|
G | A | 2 | a0001c0001t0003g0276a0002c0002t0002g0021 | 2 | HG00639.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.974-360G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135129635 | ||||||
| chr2:135129729
|
A | G | 2 | a0001c0001t0002g0149a0001c0001t0002g0193 | 2 | NA18979.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.974-266A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135129729 | ||||||
| chr2:135129813
|
A | C | 2 | a0001c0004t0013g0257a0001c0004t0026g0255 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.974-182A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | chr2 | 135129813 | ||||||
| chr2:135129944
|
AT | A | 22 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0242others(19): Show | 22 | HG00639.hp1 HG01884.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.974-38delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr2 | 135129944 | |||||
| chr2:135130198
|
C | T | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.1066+111C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 12/23 | chr2 | 135130198 | ||||||
| chr2:135130323
|
T | C | 80 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(77): Show | 80 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.1067-229T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 12/23 | chr2 | 135130323 | ||||||
| chr2:135130447
|
G | C | 1 | a0002c0002t0001g0129 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1067-105G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 12/23 | chr2 | 135130447 | ||||||
| chr2:135130508
|
G | T | 41 | a0001c0001t0002g0247a0001c0001t0003g0227a0001c0001t0003g0228others(38): Show | 41 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.1067-44G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 12/23 | chr2 | 135130508 | ||||||
| chr2:135130753
|
A | G | 3 | a0001c0007t0002g0018a0001c0007t0002g0019a0001c0007t0002g0020 | 3 | HG02280.hp2 HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1236+32A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/23 | chr2 | 135130753 | ||||||
| chr2:135130978
|
G | C | 1 | a0002c0002t0024g0108 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1236+257G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/23 | chr2 | 135130978 | ||||||
| chr2:135131064
|
C | T | 28 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(25): Show | 28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1236+343C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/23 | chr2 | 135131064 | ||||||
| chr2:135131257
|
C | T | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1236+536C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/23 | chr2 | 135131257 | ||||||
| chr2:135131479
|
C | T | 1 | a0001c0001t0002g0211 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1236+758C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/23 | chr2 | 135131479 | ||||||
| chr2:135131859
|
A | C | 1 | a0003c0006t0002g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1237-1036A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/23 | chr2 | 135131859 | ||||||
| chr2:135131873
|
A | G | 1 | a0001c0001t0002g0140 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1237-1022A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/23 | chr2 | 135131873 | ||||||
| chr2:135132142
|
G | T | 2 | a0001c0001t0015g0272a0001c0001t0015g0273 | 2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1237-753G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/23 | chr2 | 135132142 | ||||||
| chr2:135132232
|
A | G | 24 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(21): Show | 24 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.1237-663A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/23 | chr2 | 135132232 | ||||||
| chr2:135132311
|
C | T | 4 | a0001c0003t0001g0025a0001c0003t0001g0026a0001c0003t0001g0027others(1): Show | 4 | HG01243.hp2 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1237-584C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/23 | chr2 | 135132311 | ||||||
| chr2:135132416
|
G | A | 1 | a0001c0001t0003g0233 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1237-479G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/23 | chr2 | 135132416 | ||||||
| chr2:135132467
|
A | G | 1 | a0001c0001t0001g0214 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1237-428A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/23 | chr2 | 135132467 | ||||||
| chr2:135132540
|
G | A | 2 | a0001c0001t0002g0141a0001c0001t0002g0142 | 2 | NA18982.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1237-355G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/23 | chr2 | 135132540 | ||||||
| chr2:135132651
|
T | C | 4 | a0001c0001t0003g0245a0001c0001t0003g0276a0001c0001t0003g0277others(1): Show | 4 | HG00639.hp1 HG01261.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1237-244T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/23 | chr2 | 135132651 | ||||||
| chr2:135132810
|
TTAAA | T | 4 | a0003c0006t0002g0248a0003c0006t0009g0249a0003c0006t0009g0250others(1): Show | 4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1237-81_1237-78del others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr2 | 135132810 | |||||
| chr2:135133029
|
G | A | 1 | a0001c0001t0006g0223 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1326+45G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 14/23 | chr2 | 135133029 | ||||||
| chr2:135133038
|
G | C | 80 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(77): Show | 80 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.1326+54G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 14/23 | chr2 | 135133038 | ||||||
| chr2:135133467
|
G | A | 1 | a0002c0002t0001g0121 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1327-394G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 14/23 | chr2 | 135133467 | ||||||
| chr2:135133518
|
T | C | 5 | a0001c0001t0003g0277a0003c0006t0002g0248a0003c0006t0009g0249others(2): Show | 5 | HG02258.hp2 HG03041.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1327-343T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 14/23 | chr2 | 135133518 | ||||||
| chr2:135133538
|
G | A | 1 | a0001c0001t0020g0138 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1327-323G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 14/23 | chr2 | 135133538 | ||||||
| chr2:135133711
|
T | C | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1327-150T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 14/23 | chr2 | 135133711 | ||||||
| chr2:135133734
|
T | A | 2 | a0001c0001t0004g0258a0001c0001t0004g0259 | 2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1327-127T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 14/23 | chr2 | 135133734 | ||||||
| chr2:135133790
|
C | T | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1327-71C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 14/23 | chr2 | 135133790 | ||||||
| chr2:135134739
|
C | G | 3 | a0001c0001t0002g0208a0001c0001t0002g0212a0001c0001t0002g0213 | 3 | NA18990.hp1 NA19078.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1500-526C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 15/23 | chr2 | 135134739 | ||||||
| chr2:135135115
|
C | T | 4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1500-150C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 15/23 | chr2 | 135135115 | ||||||
| chr2:135135190
|
T | C | 1 | a0001c0001t0003g0275 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1500-75T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 15/23 | chr2 | 135135190 | ||||||
| chr2:135135433
|
T | C | 4 | a0003c0006t0002g0248a0003c0006t0009g0249a0003c0006t0009g0250others(1): Show | 4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1554+114T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 16/23 | chr2 | 135135433 | ||||||
| chr2:135135490
|
A | G | 1 | a0002c0002t0001g0122 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1555-74A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 16/23 | chr2 | 135135490 | ||||||
| chr2:135136001
|
T | C | 4 | a0002c0002t0001g0099a0002c0002t0001g0101a0002c0002t0001g0217others(1): Show | 4 | HG02074.hp1 HG02083.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.1923+69T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135136001 | ||||||
| chr2:135136023
|
T | G | 1 | a0001c0001t0002g0173 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1923+91T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135136023 | ||||||
| chr2:135136105
|
C | A | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1923+173C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135136105 | ||||||
| chr2:135136132
|
T | G | 1 | a0001c0001t0002g0187 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1923+200T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135136132 | ||||||
| chr2:135136283
|
A | G | 154 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(151): Show | 154 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.1923+351A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135136283 | ||||||
| chr2:135136311
|
G | A | 2 | a0001c0001t0015g0272a0001c0001t0015g0273 | 2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1923+379G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135136311 | ||||||
| chr2:135136636
|
T | C | 1 | a0001c0001t0002g0141 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1923+704T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135136636 | ||||||
| chr2:135136707
|
C | G | 1 | a0001c0004t0013g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1923+775C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135136707 | ||||||
| chr2:135136848
|
A | T | 1 | a0001c0001t0001g0036 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1923+916A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135136848 | ||||||
| chr2:135136910
|
A | G | 1 | a0002c0002t0001g0100 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1923+978A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135136910 | ||||||
| chr2:135136983
|
G | A | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1923+1051G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135136983 | ||||||
| chr2:135137096
|
A | T | 4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1923+1164A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135137096 | ||||||
| chr2:135137191
|
T | G | 14 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(11): Show | 14 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1923+1259T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135137191 | ||||||
| chr2:135137267
|
A | G | 4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1923+1335A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135137267 | ||||||
| chr2:135137288
|
G | A | 1 | a0001c0001t0002g0169 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1923+1356G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135137288 | ||||||
| chr2:135137309
|
G | T | 4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1923+1377G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135137309 | ||||||
| chr2:135137373
|
A | T | 2 | a0001c0001t0002g0167a0001c0001t0002g0200 | 2 | HG01346.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1923+1441A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135137373 | ||||||
| chr2:135137515
|
T | G | 4 | a0002c0002t0001g0114a0002c0002t0001g0115a0002c0002t0001g0116others(1): Show | 4 | HG02027.hp1 HG02129.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1923+1583T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135137515 | ||||||
| chr2:135137720
|
T | C | 1 | a0001c0001t0021g0229 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1923+1788T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135137720 | ||||||
| chr2:135137824
|
T | G | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1923+1892T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135137824 | ||||||
| chr2:135137829
|
T | G | 1 | a0002c0002t0001g0016 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1923+1897T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135137829 | ||||||
| chr2:135138003
|
T | G | 1 | a0001c0001t0003g0279 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1923+2071T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135138003 | ||||||
| chr2:135138239
|
A | G | 151 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(148): Show | 151 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.1923+2307A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135138239 | ||||||
| chr2:135138277
|
C | G | 1 | a0002c0002t0001g0121 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1923+2345C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135138277 | ||||||
| chr2:135138281
|
C | A | 2 | a0001c0001t0002g0189a0001c0001t0002g0190 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1923+2349C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135138281 | ||||||
| chr2:135138281
|
C | CA | 41 | a0001c0001t0001g0071a0001c0001t0002g0163a0001c0001t0002g0167others(38): Show | 41 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.1923+2368dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135138281 | |||||
| chr2:135138281
|
CA | C | 18 | a0001c0001t0002g0157a0001c0001t0002g0247a0001c0001t0005g0007others(15): Show | 18 | HG00280.hp1 HG00423.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1923+2368delA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135138281 | |||||
| chr2:135138300
|
A | T | 2 | a0002c0002t0001g0047a0002c0002t0001g0119 | 2 | HG00423.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1923+2368A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135138300 | ||||||
| chr2:135138309
|
C | G | 154 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(151): Show | 154 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.1923+2377C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135138309 | ||||||
| chr2:135138318
|
C | T | 1 | a0001c0001t0002g0143 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1923+2386C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135138318 | ||||||
| chr2:135138371
|
G | C | 3 | a0001c0001t0012g0252a0001c0001t0012g0253a0001c0001t0012g0254 | 3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1923+2439G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135138371 | ||||||
| chr2:135138833
|
T | A | 4 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0197others(1): Show | 4 | NA18942.hp1 NA18955.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.1923+2901T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135138833 | ||||||
| chr2:135139072
|
C | T | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1923+3140C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135139072 | ||||||
| chr2:135139101
|
C | T | 1 | a0002c0002t0001g0092 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1923+3169C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135139101 | ||||||
| chr2:135139415
|
G | A | 4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1923+3483G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135139415 | ||||||
| chr2:135139556
|
A | T | 2 | a0001c0001t0002g0079a0001c0001t0002g0191 | 2 | HG03453.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1923+3624A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135139556 | ||||||
| chr2:135139562
|
T | A | 2 | a0001c0001t0002g0205a0001c0001t0002g0207 | 2 | NA18966.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1923+3630T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135139562 | ||||||
| chr2:135139709
|
T | G | 1 | a0001c0001t0001g0036 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1923+3777T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135139709 | ||||||
| chr2:135139997
|
C | T | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1923+4065C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135139997 | ||||||
| chr2:135140065
|
G | A | 1 | a0002c0002t0001g0113 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1923+4133G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135140065 | ||||||
| chr2:135140186
|
A | C | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1923+4254A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135140186 | ||||||
| chr2:135140276
|
CTA | C | 4 | a0002c0002t0001g0099a0002c0002t0001g0101a0002c0002t0001g0217others(1): Show | 4 | HG02074.hp1 HG02083.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.1923+4348_1923+434 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135140276 | |||||
| chr2:135140453
|
C | T | 41 | a0001c0001t0002g0247a0001c0001t0003g0227a0001c0001t0003g0228others(38): Show | 41 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.1923+4521C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135140453 | ||||||
| chr2:135140504
|
A | G | 2 | a0001c0003t0001g0025a0001c0003t0001g0026 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1923+4572A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135140504 | ||||||
| chr2:135140817
|
G | A | 1 | a0001c0001t0002g0204 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1923+4885G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135140817 | ||||||
| chr2:135141222
|
T | G | 3 | a0001c0001t0002g0161a0001c0001t0002g0189a0001c0001t0002g0190 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1923+5290T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135141222 | ||||||
| chr2:135141224
|
A | ACTT | 35 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(32): Show | 35 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.1923+5296_1923+529 others(7): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135141224 | |||||
| chr2:135141228
|
C | CTTCT | 5 | a0001c0001t0002g0247a0003c0006t0002g0248a0003c0006t0009g0249others(2): Show | 5 | HG01243.hp1 HG02258.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1923+5298_1923+529 others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135141228 | |||||
| chr2:135141228
|
C | CTTCTT | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.1923+5298_1923+529 others(9): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135141228 | |||||
| chr2:135141451
|
C | G | 80 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(77): Show | 80 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.1923+5519C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135141451 | ||||||
| chr2:135141499
|
T | C | 154 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(151): Show | 154 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.1923+5567T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135141499 | ||||||
| chr2:135141772
|
G | A | 1 | a0005c0014t0002g0202 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1923+5840G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135141772 | ||||||
| chr2:135141849
|
A | G | 2 | a0002c0002t0001g0094a0002c0002t0001g0106 | 2 | NA18963.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1923+5917A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135141849 | ||||||
| chr2:135141874
|
CTATTTCT others(46): Show |
C | 1 | a0001c0001t0003g0232 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1923+5945_1923+599 others(57): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135141874 | |||||
| chr2:135142082
|
T | C | 28 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(25): Show | 28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1923+6150T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135142082 | ||||||
| chr2:135142099
|
G | A | 2 | a0001c0001t0002g0158a0001c0001t0002g0160 | 2 | NA18986.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1923+6167G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135142099 | ||||||
| chr2:135142153
|
T | C | 1 | a0001c0001t0002g0148 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1923+6221T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135142153 | ||||||
| chr2:135142297
|
T | C | 4 | a0003c0006t0002g0248a0003c0006t0009g0249a0003c0006t0009g0250others(1): Show | 4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1923+6365T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135142297 | ||||||
| chr2:135142427
|
ATTT | A | 3 | a0003c0006t0009g0249a0003c0006t0009g0250a0003c0006t0009g0251 | 3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1923+6496_1923+649 others(7): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135142427 | ||||||
| chr2:135142642
|
C | T | 1 | a0002c0002t0001g0217 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1923+6710C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135142642 | ||||||
| chr2:135142648
|
A | G | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1923+6716A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135142648 | ||||||
| chr2:135142959
|
G | T | 1 | a0001c0001t0001g0159 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1923+7027G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135142959 | ||||||
| chr2:135142969
|
C | T | 80 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(77): Show | 80 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.1923+7037C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135142969 | ||||||
| chr2:135143534
|
A | G | 1 | a0001c0001t0003g0277 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1924-6835A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135143534 | ||||||
| chr2:135143550
|
A | G | 1 | a0001c0001t0003g0279 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1924-6819A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135143550 | ||||||
| chr2:135143556
|
C | CT | 44 | a0001c0001t0001g0040a0001c0001t0003g0227a0001c0001t0003g0228others(41): Show | 44 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.1924-6794dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135143556 | |||||
| chr2:135143556
|
CT | C | 5 | a0001c0001t0002g0146a0001c0001t0005g0014a0001c0001t0012g0254others(2): Show | 5 | HG01070.hp2 HG01993.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1924-6794delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135143556 | |||||
| chr2:135143580
|
C | T | 1 | a0002c0002t0001g0129 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1924-6789C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135143580 | ||||||
| chr2:135143593
|
T | C | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1924-6776T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135143593 | ||||||
| chr2:135143800
|
C | T | 14 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(11): Show | 14 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1924-6569C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135143800 | ||||||
| chr2:135144094
|
C | T | 1 | a0001c0001t0003g0276 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1924-6275C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135144094 | ||||||
| chr2:135144176
|
C | G | 8 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(5): Show | 8 | HG01070.hp1 HG01192.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.1924-6193C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135144176 | ||||||
| chr2:135144186
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1924-6183C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135144186 | ||||||
| chr2:135144222
|
C | T | 10 | a0001c0001t0003g0234a0001c0001t0003g0235a0001c0001t0003g0236others(7): Show | 10 | HG01175.hp2 HG01884.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1924-6147C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135144222 | ||||||
| chr2:135144331
|
TTTC | T | 28 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(25): Show | 28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1924-6036_1924-603 others(7): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135144331 | |||||
| chr2:135144457
|
G | C | 1 | a0001c0001t0001g0049 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1924-5912G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135144457 | ||||||
| chr2:135144602
|
C | A | 55 | a0001c0001t0002g0247a0001c0001t0003g0227a0001c0001t0003g0228others(52): Show | 55 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1924-5767C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135144602 | ||||||
| chr2:135144650
|
C | T | 55 | a0001c0001t0002g0247a0001c0001t0003g0227a0001c0001t0003g0228others(52): Show | 55 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1924-5719C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135144650 | ||||||
| chr2:135144671
|
T | G | 1 | a0002c0002t0001g0113 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1924-5698T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135144671 | ||||||
| chr2:135144843
|
G | A | 3 | a0003c0006t0009g0249a0003c0006t0009g0250a0003c0006t0009g0251 | 3 | HG02258.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1924-5526G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135144843 | ||||||
| chr2:135145301
|
C | T | 1 | a0001c0001t0010g0209 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1924-5068C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135145301 | ||||||
| chr2:135145360
|
A | T | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1924-5009A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135145360 | ||||||
| chr2:135145399
|
T | TAC | 5 | a0001c0001t0001g0084a0001c0001t0003g0240a0001c0001t0012g0252others(2): Show | 5 | HG01175.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1924-4947_1924-494 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135145399 | |||||
| chr2:135145399
|
TAC | T | 98 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(95): Show | 98 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(95): Show |
intron_variant | MODIFIER | c.1924-4947_1924-494 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135145399 | |||||
| chr2:135145399
|
TACAC | T | 16 | a0001c0001t0002g0176a0001c0001t0002g0188a0001c0001t0002g0191others(13): Show | 16 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.1924-4949_1924-494 others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135145399 | |||||
| chr2:135145399
|
TACACACA others(3): Show |
T | 2 | a0001c0001t0015g0272a0001c0001t0015g0273 | 2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1924-4955_1924-494 others(14): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135145399 | |||||
| chr2:135145469
|
C | T | 1 | a0001c0001t0002g0168 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1924-4900C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135145469 | ||||||
| chr2:135146199
|
C | CT | 91 | a0001c0001t0001g0030a0001c0001t0001g0066a0001c0001t0001g0159others(88): Show | 91 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.1924-4147dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135146199 | |||||
| chr2:135146199
|
C | CTT | 8 | a0001c0001t0001g0040a0001c0001t0005g0015a0001c0001t0012g0252others(5): Show | 8 | HG02258.hp2 HG02293.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1924-4148_1924-414 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135146199 | |||||
| chr2:135146199
|
CT | C | 5 | a0001c0001t0002g0148a0001c0001t0002g0157a0001c0001t0002g0247others(2): Show | 5 | HG01243.hp1 HG03490.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.1924-4147delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135146199 | |||||
| chr2:135146199
|
CTTTTTTT others(5): Show |
C | 1 | a0002c0002t0001g0100 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1924-4158_1924-414 others(16): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135146199 | |||||
| chr2:135146216
|
T | C | 3 | a0001c0004t0013g0256a0001c0004t0013g0257a0001c0004t0026g0255 | 3 | HG03130.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1924-4153T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135146216 | ||||||
| chr2:135146302
|
G | C | 1 | a0001c0001t0001g0039 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1924-4067G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135146302 | ||||||
| chr2:135146632
|
C | T | 4 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0001t0002g0207others(1): Show | 4 | NA18952.hp2 NA18966.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.1924-3737C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135146632 | ||||||
| chr2:135146713
|
A | G | 1 | a0002c0002t0001g0100 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1924-3656A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135146713 | ||||||
| chr2:135146810
|
A | T | 2 | a0001c0001t0002g0167a0001c0001t0002g0200 | 2 | HG01346.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1924-3559A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135146810 | ||||||
| chr2:135146854
|
A | AAC | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.1924-3514_1924-351 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135146854 | |||||
| chr2:135146939
|
T | G | 1 | a0006c0013t0005g0004 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1924-3430T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135146939 | ||||||
| chr2:135146971
|
A | AAC | 93 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0049others(90): Show | 93 | HG00438.hp1 HG00621.hp2 HG00741.hp2 others(90): Show |
intron_variant | MODIFIER | c.1924-3371_1924-337 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135146971 | |||||
| chr2:135146971
|
A | AACAC | 13 | a0001c0001t0002g0196a0001c0001t0002g0210a0001c0004t0013g0246others(10): Show | 13 | HG02258.hp2 HG02895.hp1 HG02897.hp1 others(10): Show |
intron_variant | MODIFIER | c.1924-3373_1924-337 others(8): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135146971 | |||||
| chr2:135146971
|
A | AACACAC | 4 | a0001c0001t0002g0162a0001c0001t0012g0252a0001c0001t0012g0253others(1): Show | 4 | HG02809.hp2 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1924-3375_1924-337 others(10): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135146971 | |||||
| chr2:135146971
|
AAC | A | 40 | a0001c0001t0001g0080a0001c0001t0002g0161a0001c0001t0002g0247others(37): Show | 40 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.1924-3371_1924-337 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135146971 | |||||
| chr2:135147089
|
T | A | 4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1924-3280T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135147089 | ||||||
| chr2:135147098
|
C | T | 8 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(5): Show | 8 | HG02895.hp1 HG02897.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.1924-3271C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135147098 | ||||||
| chr2:135147301
|
G | A | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.1924-3068G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135147301 | ||||||
| chr2:135147345
|
C | CA | 6 | a0001c0001t0001g0051a0001c0001t0002g0155a0001c0001t0002g0186others(3): Show | 6 | HG00621.hp2 HG01978.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.1924-3008dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135147345 | |||||
| chr2:135147426
|
T | C | 2 | a0001c0001t0003g0277a0001c0001t0003g0279 | 2 | HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1924-2943T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135147426 | ||||||
| chr2:135147615
|
T | TC | 22 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0140others(19): Show | 22 | HG01346.hp2 HG01981.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1924-2745dupC | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135147615 | |||||
| chr2:135147615
|
T | TCC | 37 | a0001c0001t0002g0141a0001c0001t0002g0146a0001c0001t0002g0147others(34): Show | 37 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.1924-2746_1924-274 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135147615 | |||||
| chr2:135147615
|
T | TCCC | 16 | a0001c0001t0002g0139a0001c0001t0002g0142a0001c0001t0002g0150others(13): Show | 16 | HG01192.hp1 HG01928.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.1924-2747_1924-274 others(7): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135147615 | |||||
| chr2:135147623
|
C | G | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1924-2746C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135147623 | ||||||
| chr2:135147624
|
C | CT | 28 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(25): Show | 28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1924-2735dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135147624 | |||||
| chr2:135147625
|
T | C | 3 | a0001c0001t0002g0149a0001c0001t0002g0193a0001c0001t0004g0263 | 3 | HG03225.hp1 NA18979.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1924-2744T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135147625 | ||||||
| chr2:135147786
|
A | C | 3 | a0001c0001t0012g0252a0001c0001t0012g0253a0001c0001t0012g0254 | 3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1924-2583A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135147786 | ||||||
| chr2:135147993
|
C | CCT | 270 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0029others(267): Show | 271 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(268): Show |
intron_variant | MODIFIER | c.1924-2372_1924-237 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135147993 | |||||
| chr2:135148341
|
C | T | 2 | a0001c0001t0002g0139a0001c0001t0002g0171 | 2 | HG02056.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1924-2028C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135148341 | ||||||
| chr2:135148379
|
C | T | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1924-1990C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135148379 | ||||||
| chr2:135148491
|
CT | C | 145 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0029others(142): Show | 146 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.1924-1857delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135148491 | |||||
| chr2:135148491
|
CTT | C | 55 | a0001c0001t0001g0051a0001c0001t0002g0181a0001c0001t0002g0183others(52): Show | 55 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1924-1858_1924-185 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135148491 | |||||
| chr2:135148668
|
C | CT | 31 | a0001c0001t0003g0230a0001c0001t0003g0234a0001c0001t0003g0235others(28): Show | 31 | HG00735.hp2 HG01175.hp2 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.1924-1679dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135148668 | |||||
| chr2:135148668
|
CT | C | 11 | a0001c0001t0002g0165a0001c0001t0002g0171a0001c0001t0002g0181others(8): Show | 11 | HG01070.hp1 HG01256.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1924-1679delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135148668 | |||||
| chr2:135148668
|
CTT | C | 5 | a0001c0001t0002g0247a0003c0006t0002g0248a0004c0005t0011g0219others(2): Show | 5 | HG01243.hp1 HG02895.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1924-1680_1924-167 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135148668 | |||||
| chr2:135148668
|
CTTT | C | 15 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(12): Show | 15 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.1924-1681_1924-167 others(7): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135148668 | |||||
| chr2:135148708
|
C | T | 2 | a0001c0001t0002g0158a0001c0001t0002g0160 | 2 | NA18986.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1924-1661C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135148708 | ||||||
| chr2:135148731
|
C | CG | 28 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(25): Show | 28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1924-1637dupG | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 135148731 | |||||
| chr2:135148732
|
G | A | 9 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(6): Show | 9 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.1924-1637G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135148732 | ||||||
| chr2:135149016
|
A | G | 6 | a0001c0001t0002g0156a0001c0001t0002g0168a0001c0001t0002g0169others(3): Show | 6 | HG00438.hp1 HG02040.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.1924-1353A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135149016 | ||||||
| chr2:135149044
|
A | G | 1 | a0001c0001t0017g0226 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1924-1325A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135149044 | ||||||
| chr2:135149122
|
T | G | 28 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(25): Show | 28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1924-1247T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135149122 | ||||||
| chr2:135149509
|
C | T | 1 | a0006c0013t0005g0004 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1924-860C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135149509 | ||||||
| chr2:135149518
|
A | G | 264 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0029others(261): Show | 265 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(262): Show |
intron_variant | MODIFIER | c.1924-851A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135149518 | ||||||
| chr2:135149635
|
A | G | 1 | a0001c0001t0007g0144 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1924-734A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135149635 | ||||||
| chr2:135149661
|
A | G | 3 | a0001c0001t0005g0008a0001c0001t0005g0012a0001c0001t0005g0013 | 3 | NA19002.hp1 NA19006.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1924-708A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135149661 | ||||||
| chr2:135149869
|
G | A | 3 | a0001c0001t0012g0252a0001c0001t0012g0253a0001c0001t0012g0254 | 3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1924-500G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135149869 | ||||||
| chr2:135150003
|
A | T | 1 | a0001c0001t0003g0279 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1924-366A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135150003 | ||||||
| chr2:135150276
|
T | C | 40 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(37): Show | 40 | HG00438.hp1 HG01346.hp2 HG01978.hp2 others(37): Show |
intron_variant | MODIFIER | c.1924-93T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135150276 | ||||||
| chr2:135150308
|
T | C | 1 | a0001c0001t0002g0177 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1924-61T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 17/23 | chr2 | 135150308 | ||||||
| chr2:135150654
|
C | T | 1 | a0001c0001t0003g0279 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2061+148C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 18/23 | chr2 | 135150654 | ||||||
| chr2:135150775
|
G | A | 1 | a0001c0001t0002g0165 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2061+269G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 18/23 | chr2 | 135150775 | ||||||
| chr2:135151215
|
A | G | 1 | a0001c0008t0008g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2061+709A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 18/23 | chr2 | 135151215 | ||||||
| chr2:135151581
|
C | T | 3 | a0001c0001t0002g0204a0001c0001t0002g0211a0001c0001t0010g0209 | 3 | HG03017.hp2 HG03654.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.2061+1075C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 18/23 | chr2 | 135151581 | ||||||
| chr2:135151892
|
G | A | 154 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(151): Show | 154 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.2061+1386G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 18/23 | chr2 | 135151892 | ||||||
| chr2:135151938
|
T | C | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2061+1432T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 18/23 | chr2 | 135151938 | ||||||
| chr2:135152077
|
T | C | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2061+1571T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 18/23 | chr2 | 135152077 | ||||||
| chr2:135152337
|
C | T | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2062-1312C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 18/23 | chr2 | 135152337 | ||||||
| chr2:135152350
|
G | C | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.2062-1299G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 18/23 | chr2 | 135152350 | ||||||
| chr2:135152421
|
T | C | 1 | a0001c0003t0001g0027 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2062-1228T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 18/23 | chr2 | 135152421 | ||||||
| chr2:135152748
|
T | A | 1 | a0001c0001t0001g0022 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2062-901T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 18/23 | chr2 | 135152748 | ||||||
| chr2:135152845
|
G | A | 4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.2062-804G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 18/23 | chr2 | 135152845 | ||||||
| chr2:135152975
|
A | G | 1 | a0001c0007t0002g0019 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2062-674A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 18/23 | chr2 | 135152975 | ||||||
| chr2:135153177
|
CTG | C | 4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.2062-468_2062-467d others(4): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr2 | 135153177 | |||||
| chr2:135153192
|
C | A | 1 | a0001c0001t0001g0073 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2062-457C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 18/23 | chr2 | 135153192 | ||||||
| chr2:135154435
|
C | T | 5 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0081others(2): Show | 5 | HG00735.hp1 HG01358.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2289+559C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135154435 | ||||||
| chr2:135154456
|
A | G | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.2289+580A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135154456 | ||||||
| chr2:135154465
|
A | C | 1 | a0007c0011t0014g0278 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2289+589A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135154465 | ||||||
| chr2:135154473
|
T | TTACTAAG others(3): Show |
16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.2289+600_2289+609d others(12): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr2 | 135154473 | |||||
| chr2:135154549
|
C | A | 1 | a0001c0001t0001g0049 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2289+673C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135154549 | ||||||
| chr2:135154685
|
A | G | 80 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(77): Show | 80 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.2289+809A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135154685 | ||||||
| chr2:135154707
|
C | G | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2289+831C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135154707 | ||||||
| chr2:135155043
|
A | T | 3 | a0001c0001t0001g0036a0001c0001t0001g0102a0001c0001t0001g0105 | 3 | HG03491.hp2 HG03492.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.2289+1167A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135155043 | ||||||
| chr2:135155075
|
T | C | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2289+1199T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135155075 | ||||||
| chr2:135155389
|
T | C | 1 | a0001c0001t0004g0262 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2289+1513T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135155389 | ||||||
| chr2:135155407
|
G | T | 148 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(145): Show | 148 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(145): Show |
intron_variant | MODIFIER | c.2289+1531G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135155407 | ||||||
| chr2:135155476
|
T | A | 5 | a0001c0001t0002g0147a0001c0001t0002g0150a0001c0001t0002g0151others(2): Show | 5 | HG00741.hp2 HG01256.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.2289+1600T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135155476 | ||||||
| chr2:135155676
|
A | G | 1 | a0001c0003t0001g0027 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2289+1800A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135155676 | ||||||
| chr2:135156458
|
T | C | 2 | a0001c0001t0010g0179a0001c0001t0010g0180 | 2 | NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2289+2582T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135156458 | ||||||
| chr2:135156468
|
C | T | 151 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(148): Show | 151 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.2289+2592C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135156468 | ||||||
| chr2:135156556
|
T | C | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.2289+2680T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135156556 | ||||||
| chr2:135156582
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG02886.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2289+2706G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135156582 | ||||||
| chr2:135156652
|
A | G | 1 | a0001c0001t0002g0186 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2289+2776A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135156652 | ||||||
| chr2:135156799
|
C | G | 10 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(7): Show | 10 | HG03017.hp2 HG03654.hp1 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.2289+2923C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135156799 | ||||||
| chr2:135157072
|
C | T | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2289+3196C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135157072 | ||||||
| chr2:135157083
|
C | T | 96 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(93): Show | 96 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(93): Show |
intron_variant | MODIFIER | c.2289+3207C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135157083 | ||||||
| chr2:135157109
|
G | A | 3 | a0001c0007t0002g0018a0001c0007t0002g0019a0001c0007t0002g0020 | 3 | HG02280.hp2 HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2289+3233G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135157109 | ||||||
| chr2:135157344
|
A | C | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.2289+3468A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135157344 | ||||||
| chr2:135157378
|
C | G | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2289+3502C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135157378 | ||||||
| chr2:135157431
|
C | T | 4 | a0003c0006t0002g0248a0003c0006t0009g0249a0003c0006t0009g0250others(1): Show | 4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2289+3555C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135157431 | ||||||
| chr2:135157620
|
T | C | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2289+3744T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135157620 | ||||||
| chr2:135157788
|
T | C | 217 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0102others(214): Show | 218 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.2289+3912T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135157788 | ||||||
| chr2:135157831
|
C | CA | 8 | a0001c0001t0001g0040a0001c0001t0018g0074a0002c0002t0001g0075others(5): Show | 8 | HG01192.hp2 HG02056.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.2289+3973dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr2 | 135157831 | |||||
| chr2:135157831
|
CA | C | 136 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(133): Show | 136 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.2289+3973delA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr2 | 135157831 | |||||
| chr2:135157831
|
CAA | C | 10 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(7): Show | 10 | HG02055.hp1 HG02280.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.2289+3972_2289+397 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr2 | 135157831 | |||||
| chr2:135157839
|
A | C | 1 | a0001c0001t0001g0090 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2289+3963A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135157839 | ||||||
| chr2:135157844
|
A | C | 80 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(77): Show | 80 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.2289+3968A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135157844 | ||||||
| chr2:135157846
|
A | AC | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2289+3970_2289+397 others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135157846 | ||||||
| chr2:135157850
|
C | A | 1 | a0001c0001t0001g0084 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2289+3974C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135157850 | ||||||
| chr2:135158187
|
A | G | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.2289+4311A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135158187 | ||||||
| chr2:135158207
|
C | T | 1 | a0001c0001t0003g0276 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2289+4331C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135158207 | ||||||
| chr2:135158300
|
G | A | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.2290-4255G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135158300 | ||||||
| chr2:135158426
|
T | C | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2290-4129T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135158426 | ||||||
| chr2:135158597
|
A | G | 1 | a0001c0004t0013g0256 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2290-3958A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135158597 | ||||||
| chr2:135158642
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2290-3913A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135158642 | ||||||
| chr2:135158920
|
C | T | 1 | a0001c0004t0013g0256 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2290-3635C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135158920 | ||||||
| chr2:135158938
|
C | G | 1 | a0002c0002t0002g0021 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2290-3617C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135158938 | ||||||
| chr2:135159053
|
C | G | 2 | a0001c0001t0002g0158a0001c0001t0002g0160 | 2 | NA18986.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2290-3502C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135159053 | ||||||
| chr2:135159316
|
C | T | 1 | a0001c0001t0004g0259 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2290-3239C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135159316 | ||||||
| chr2:135159381
|
C | T | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.2290-3174C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135159381 | ||||||
| chr2:135159656
|
G | T | 1 | a0001c0008t0008g0005 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2290-2899G>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135159656 | ||||||
| chr2:135159677
|
G | A | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.2290-2878G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135159677 | ||||||
| chr2:135159681
|
A | G | 6 | a0001c0001t0002g0139a0001c0001t0002g0155a0001c0001t0002g0167others(3): Show | 6 | HG01346.hp2 HG01978.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.2290-2874A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135159681 | ||||||
| chr2:135159889
|
G | C | 9 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(6): Show | 9 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.2290-2666G>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135159889 | ||||||
| chr2:135160327
|
A | G | 1 | a0001c0001t0001g0218 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2290-2228A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135160327 | ||||||
| chr2:135160354
|
T | C | 4 | a0001c0004t0013g0246a0001c0004t0013g0256a0001c0004t0013g0257others(1): Show | 4 | HG03130.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.2290-2201T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135160354 | ||||||
| chr2:135160399
|
C | T | 4 | a0004c0005t0011g0219a0004c0005t0011g0220a0004c0005t0011g0222others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2290-2156C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135160399 | ||||||
| chr2:135160530
|
G | A | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2290-2025G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135160530 | ||||||
| chr2:135160542
|
C | G | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.2290-2013C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135160542 | ||||||
| chr2:135160597
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2290-1958C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135160597 | ||||||
| chr2:135160674
|
C | CA | 16 | a0001c0001t0001g0040a0001c0001t0001g0048a0001c0001t0001g0082others(13): Show | 16 | HG00438.hp2 HG00639.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.2290-1855dupA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr2 | 135160674 | |||||
| chr2:135160674
|
CA | C | 45 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0066others(42): Show | 45 | HG00280.hp1 HG00741.hp2 HG01256.hp2 others(42): Show |
intron_variant | MODIFIER | c.2290-1855delA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr2 | 135160674 | |||||
| chr2:135160674
|
CAA | C | 66 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(63): Show | 66 | HG00438.hp1 HG01070.hp1 HG01192.hp1 others(63): Show |
intron_variant | MODIFIER | c.2290-1856_2290-185 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr2 | 135160674 | |||||
| chr2:135160674
|
CAAA | C | 18 | a0001c0001t0002g0157a0001c0001t0002g0166a0001c0001t0004g0258others(15): Show | 18 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.2290-1857_2290-185 others(7): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr2 | 135160674 | |||||
| chr2:135160732
|
A | G | 1 | a0002c0002t0001g0109 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2290-1823A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135160732 | ||||||
| chr2:135160798
|
C | A | 1 | a0001c0001t0001g0052 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2290-1757C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135160798 | ||||||
| chr2:135161111
|
A | G | 79 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(76): Show | 79 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(76): Show |
intron_variant | MODIFIER | c.2290-1444A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135161111 | ||||||
| chr2:135161145
|
A | G | 1 | a0002c0002t0001g0069 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2290-1410A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135161145 | ||||||
| chr2:135161320
|
T | C | 5 | a0001c0001t0004g0259a0004c0005t0011g0219a0004c0005t0011g0220others(2): Show | 5 | HG02895.hp1 HG02897.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2290-1235T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135161320 | ||||||
| chr2:135161350
|
A | G | 1 | a0001c0001t0003g0277 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2290-1205A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135161350 | ||||||
| chr2:135161391
|
GA | G | 5 | a0001c0001t0003g0234a0001c0001t0003g0237a0001c0001t0003g0240others(2): Show | 5 | HG01175.hp2 HG02109.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2290-1157delA | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr2 | 135161391 | |||||
| chr2:135161802
|
A | G | 3 | a0001c0001t0005g0009a0001c0001t0005g0014a0001c0001t0005g0015 | 3 | HG01358.hp2 HG01993.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.2290-753A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135161802 | ||||||
| chr2:135161891
|
A | T | 2 | a0001c0001t0002g0158a0001c0001t0002g0160 | 2 | NA18986.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2290-664A>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135161891 | ||||||
| chr2:135161979
|
A | G | 1 | a0001c0001t0002g0186 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2290-576A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135161979 | ||||||
| chr2:135162214
|
G | A | 7 | a0002c0002t0001g0076a0002c0002t0001g0077a0002c0002t0001g0086others(4): Show | 7 | HG00738.hp1 HG01943.hp1 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.2290-341G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135162214 | ||||||
| chr2:135162357
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2290-198A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135162357 | ||||||
| chr2:135162363
|
A | G | 1 | a0001c0001t0002g0208 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2290-192A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135162363 | ||||||
| chr2:135162521
|
C | T | 33 | a0001c0001t0002g0247a0001c0001t0003g0227a0001c0001t0003g0228others(30): Show | 33 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.2290-34C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135162521 | ||||||
| chr2:135162522
|
G | A | 1 | a0001c0001t0010g0209 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2290-33G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135162522 | ||||||
| chr2:135162538
|
C | T | 28 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(25): Show | 28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.2290-17C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 19/23 | chr2 | 135162538 | ||||||
| chr2:135162953
|
C | T | 3 | a0001c0001t0012g0252a0001c0001t0012g0253a0001c0001t0012g0254 | 3 | HG02809.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2491-33C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 21/23 | chr2 | 135162953 | ||||||
| chr2:135163223
|
A | G | 8 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(5): Show | 8 | HG01070.hp1 HG01192.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.2606+122A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 22/23 | chr2 | 135163223 | ||||||
| chr2:135163704
|
G | A | 4 | a0003c0006t0002g0248a0003c0006t0009g0249a0003c0006t0009g0250others(1): Show | 4 | HG02258.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2606+603G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 22/23 | chr2 | 135163704 | ||||||
| chr2:135164169
|
G | A | 1 | a0007c0011t0014g0278 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2607-425G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 22/23 | chr2 | 135164169 | ||||||
| chr2:135164269
|
T | A | 151 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(148): Show | 151 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.2607-325T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 22/23 | chr2 | 135164269 | ||||||
| chr2:135164410
|
T | A | 1 | a0001c0001t0007g0154 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2607-184T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 22/23 | chr2 | 135164410 | ||||||
| chr2:135164720
|
C | A | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.2709+24C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135164720 | ||||||
| chr2:135165334
|
T | G | 1 | a0001c0001t0003g0232 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2709+638T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135165334 | ||||||
| chr2:135165375
|
G | A | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.2709+679G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135165375 | ||||||
| chr2:135165394
|
C | T | 4 | a0002c0002t0001g0099a0002c0002t0001g0101a0002c0002t0001g0217others(1): Show | 4 | HG02074.hp1 HG02083.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.2709+698C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135165394 | ||||||
| chr2:135165501
|
TAAC | T | 28 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(25): Show | 28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.2709+809_2709+811d others(5): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr2 | 135165501 | |||||
| chr2:135165577
|
T | C | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.2709+881T>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135165577 | ||||||
| chr2:135165908
|
G | A | 1 | a0001c0001t0002g0161 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2709+1212G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135165908 | ||||||
| chr2:135166537
|
C | T | 9 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(6): Show | 9 | HG01070.hp1 HG01192.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.2709+1841C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135166537 | ||||||
| chr2:135166555
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2709+1859C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135166555 | ||||||
| chr2:135166588
|
A | G | 1 | a0002c0002t0001g0094 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2709+1892A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135166588 | ||||||
| chr2:135166590
|
T | G | 1 | a0006c0013t0005g0004 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2709+1894T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135166590 | ||||||
| chr2:135166735
|
A | C | 1 | a0001c0001t0021g0229 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2710-1810A>C | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135166735 | ||||||
| chr2:135166855
|
C | G | 5 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0081others(2): Show | 5 | HG00735.hp1 HG01358.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2710-1690C>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135166855 | ||||||
| chr2:135166855
|
C | T | 14 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.2710-1690C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135166855 | ||||||
| chr2:135166897
|
A | G | 58 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(55): Show | 58 | HG00438.hp1 HG00741.hp2 HG01256.hp2 others(55): Show |
intron_variant | MODIFIER | c.2710-1648A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135166897 | ||||||
| chr2:135167217
|
A | G | 16 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.2710-1328A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135167217 | ||||||
| chr2:135167379
|
C | CT | 5 | a0001c0001t0002g0212a0001c0001t0007g0154a0001c0003t0001g0056others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.2710-1152dupT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr2 | 135167379 | |||||
| chr2:135167379
|
C | CTT | 27 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(24): Show | 27 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.2710-1153_2710-115 others(6): Show |
RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr2 | 135167379 | |||||
| chr2:135167379
|
CT | C | 9 | a0001c0001t0002g0173a0001c0001t0004g0260a0001c0001t0004g0261others(6): Show | 9 | HG02451.hp2 HG02622.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2710-1152delT | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr2 | 135167379 | |||||
| chr2:135167432
|
T | G | 151 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0139others(148): Show | 151 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.2710-1113T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135167432 | ||||||
| chr2:135167841
|
C | T | 2 | a0001c0003t0001g0042a0001c0003t0001g0085 | 2 | HG02258.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2710-704C>T | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135167841 | ||||||
| chr2:135167924
|
T | A | 1 | a0001c0001t0002g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2710-621T>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135167924 | ||||||
| chr2:135168021
|
A | G | 5 | a0001c0001t0003g0227a0001c0001t0003g0244a0001c0001t0006g0225others(2): Show | 5 | HG00558.hp1 HG00621.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.2710-524A>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135168021 | ||||||
| chr2:135168053
|
G | A | 24 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0230others(21): Show | 24 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.2710-492G>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135168053 | ||||||
| chr2:135168262
|
T | G | 2 | a0001c0001t0002g0189a0001c0001t0002g0190 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2710-283T>G | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135168262 | ||||||
| chr2:135168426
|
C | A | 1 | a0001c0001t0002g0205 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2710-119C>A | RAB3GAP1 | ENSG00000115839.19 | transcript | ENST00000264158.13 | protein_coding | 23/23 | chr2 | 135168426 |