Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 27342 |
|---|---|
| ensemblid | ENSG00000154710.18 |
| hgncid | 17676 |
| symbol | RABGEF1 |
| name | RAB guanine nucleotide exchange factor 1 |
| refseq_nuc | NM_014504.3 |
| refseq_prot | NP_055319.1 |
| ensembl_nuc | ENST00000284957.9 |
| ensembl_prot | ENSP00000284957.4 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 66740733 |
| end | 66811464 |
| strand | + |
| ver | v1.2 |
| region | chr7:66740733-66811464 |
| region5000 | chr7:66735733-66816464 |
| regionname0 | RABGEF1_chr7_66740733_66811464 |
| regionname5000 | RABGEF1_chr7_66735733_66816464 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 491 | 398 | 90 | 72 | 184 | 12 | 38 | 140 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| a0002 | 0/0 | 491 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1476 | 396 | 90 | 72 | 183 | 12 | 37 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| c0002 | 0/0 | 1476 | 2 | 2 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| c0003 | 0/0 | 1476 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| c0004 | 0/0 | 1476 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 2260 | 190 | 49 | 38 | 73 | 8 | 21 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| t0002 | 0/0 | 2261 | 56 | 5 | 11 | 35 | 2 | 3 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| t0003 | 0/0 | 2260 | 52 | 18 | 6 | 18 | 0 | 10 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| t0004 | 0/0 | 2260 | 28 | 1 | 5 | 20 | 2 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| t0005 | 0/0 | 2260 | 25 | 0 | 2 | 23 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| t0006 | 0/0 | 2260 | 21 | 0 | 7 | 13 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| t0007 | 0/0 | 2260 | 15 | 15 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| t0008 | 0/0 | 2261 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| t0009 | 0/0 | 2261 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| t0010 | 0/0 | 2270 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| t0011 | 0/0 | 2260 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| t0012 | 0/0 | 2260 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| t0013 | 0/0 | 2260 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| t0014 | 0/0 | 2260 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| t0015 | 0/0 | 2260 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| t0016 | 0/0 | 2260 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| t0017 | 0/0 | 2260 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| t0018 | 0/0 | 2260 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| t0019 | 0/0 | 2260 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| t0020 | 1/0 | 2258 | 1 | 0 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 5 | 0 | 0 | 4 | 1 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0003 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0010 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0100 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0221 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0372 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0373 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1476 | 396 | 90 | 72 | 183 | 12 | 37 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| a0001c0003 | 0/0 | 1476 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| a0001c0004 | 0/0 | 1476 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| a0002c0002 | 0/0 | 1476 | 2 | 2 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3735 | 186 | 47 | 38 | 72 | 8 | 20 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| a0001c0001t0002 | 0/0 | 3736 | 56 | 5 | 11 | 35 | 2 | 3 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| a0001c0001t0003 | 0/0 | 3735 | 52 | 18 | 6 | 18 | 0 | 10 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| a0001c0001t0004 | 0/0 | 3735 | 28 | 1 | 5 | 20 | 2 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| a0001c0001t0005 | 0/0 | 3735 | 25 | 0 | 2 | 23 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| a0001c0001t0006 | 0/0 | 3735 | 21 | 0 | 7 | 13 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| a0001c0001t0007 | 0/0 | 3735 | 15 | 15 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| a0001c0001t0008 | 0/0 | 3736 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| a0001c0001t0009 | 0/0 | 3736 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| a0001c0001t0010 | 0/0 | 3745 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| a0001c0001t0011 | 0/0 | 3735 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| a0001c0001t0012 | 0/0 | 3735 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| a0001c0001t0013 | 0/0 | 3735 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| a0001c0001t0014 | 0/0 | 3735 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| a0001c0001t0015 | 0/0 | 3735 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| a0001c0001t0016 | 0/0 | 3735 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| a0001c0001t0017 | 0/0 | 3735 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| a0001c0001t0018 | 0/0 | 3735 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| a0001c0001t0019 | 0/0 | 3735 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| a0001c0001t0020 | 1/0 | 3733 | 1 | 0 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| a0001c0003t0001 | 0/0 | 3735 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| a0001c0004t0001 | 0/0 | 3735 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| a0002c0002t0001 | 0/0 | 3735 | 2 | 2 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | copy fasta | chr7 | 66735733 | 66816464 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0010 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0100 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0001 | 0/0 | 5 | 0 | 0 | 4 | 1 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0372 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0004g0373 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0005g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0006g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0007g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0007g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0007g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0007g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0007g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0007g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0007g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0007g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0007g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0007g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0007g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0007g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0007g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0007g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0007g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0008g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0009g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0010g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0011g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0012g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0013g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0014g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0015g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0016g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0017g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0018g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0019g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0001t0020g0221 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0001c0004t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0002c0002t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| a0002c0002t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0297 | EUR | GBR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0302 | EUR | GBR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | FIN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00408 | hp2 | a0001 | c0001 | t0006 | g0013 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00438 | hp2 | a0001 | c0001 | t0005 | g0320 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00558 | hp2 | a0001 | c0001 | t0010 | g0074 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | CHS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0342 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0354 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00735 | hp2 | a0001 | c0001 | t0017 | g0186 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01074 | hp2 | a0001 | c0001 | t0006 | g0162 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01099 | hp1 | a0001 | c0001 | t0006 | g0013 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0181 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0187 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0137 | AMR | PUR | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0347 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0192 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0345 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0057 | EUR | IBS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0372 | EUR | IBS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0242 | EUR | IBS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0373 | EUR | IBS | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0228 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0254 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0315 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01928 | hp2 | a0001 | c0001 | t0006 | g0149 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0319 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0336 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01943 | hp2 | a0001 | c0001 | t0006 | g0159 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01952 | hp1 | a0001 | c0001 | t0006 | g0179 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01975 | hp1 | a0001 | c0001 | t0006 | g0180 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0335 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02004 | hp1 | a0001 | c0001 | t0014 | g0112 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02004 | hp2 | a0001 | c0001 | t0006 | g0160 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02027 | hp2 | a0001 | c0001 | t0018 | g0032 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02040 | hp1 | a0001 | c0004 | t0001 | g0261 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0093 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02056 | hp1 | a0001 | c0001 | t0006 | g0164 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02080 | hp2 | a0001 | c0001 | t0006 | g0175 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02148 | hp2 | a0001 | c0001 | t0013 | g0176 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0346 | EAS | CDX | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CDX | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0357 | EAS | CDX | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CDX | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0247 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0374 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0359 | AMR | PEL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02523 | hp2 | a0001 | c0001 | t0005 | g0329 | EAS | KHV | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0253 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02615 | hp2 | a0001 | c0001 | t0011 | g0085 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0248 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0142 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0307 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0165 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0304 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0134 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0080 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0138 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0249 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0250 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0334 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0375 | AFR | MSL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03098 | hp2 | a0001 | c0001 | t0008 | g0076 | AFR | MSL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0139 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0305 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0251 | AFR | MSL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0083 | AFR | MSL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | MSL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0196 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0246 | AFR | MSL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0082 | AFR | MSL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0333 | AFR | MSL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0150 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0145 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0178 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03688 | hp1 | a0001 | c0001 | t0015 | g0151 | SAS | STU | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03688 | hp2 | a0001 | c0003 | t0001 | g0124 | SAS | STU | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0184 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0146 | SAS | BEB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03942 | hp2 | a0001 | c0001 | t0006 | g0185 | SAS | BEB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0129 | SAS | BEB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0284 | SAS | BEB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | STU | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG04199 | hp2 | a0001 | c0001 | t0016 | g0296 | SAS | STU | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0166 | SAS | STU | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | STU | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG04228 | hp1 | a0001 | c0001 | t0009 | g0201 | SAS | STU | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | STU | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0361 | EAS | CHB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18906 | hp1 | a0001 | c0001 | t0012 | g0204 | AFR | YRI | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0252 | AFR | YRI | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0349 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18939 | hp2 | a0001 | c0001 | t0005 | g0331 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18943 | hp1 | a0001 | c0001 | t0006 | g0174 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18944 | hp1 | a0001 | c0001 | t0006 | g0163 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18947 | hp2 | a0001 | c0001 | t0005 | g0327 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18949 | hp1 | a0001 | c0001 | t0005 | g0328 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0352 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18950 | hp2 | a0001 | c0001 | t0005 | g0325 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0371 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0368 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0362 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0350 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18963 | hp2 | a0001 | c0001 | t0005 | g0318 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18966 | hp2 | a0001 | c0001 | t0006 | g0173 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0358 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0366 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18970 | hp2 | a0001 | c0001 | t0005 | g0312 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18971 | hp2 | a0001 | c0001 | t0006 | g0158 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0363 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18975 | hp2 | a0001 | c0001 | t0005 | g0324 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0322 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18980 | hp2 | a0001 | c0001 | t0004 | g0348 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18982 | hp2 | a0001 | c0001 | t0004 | g0341 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18985 | hp2 | a0001 | c0001 | t0005 | g0326 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18990 | hp1 | a0001 | c0001 | t0005 | g0321 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18990 | hp2 | a0001 | c0001 | t0006 | g0177 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0370 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18992 | hp2 | a0001 | c0001 | t0005 | g0332 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18994 | hp1 | a0001 | c0001 | t0005 | g0309 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0355 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19000 | hp2 | a0001 | c0001 | t0005 | g0311 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19002 | hp1 | a0001 | c0001 | t0005 | g0330 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0343 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0351 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19009 | hp1 | a0001 | c0001 | t0006 | g0183 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0340 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19010 | hp1 | a0001 | c0001 | t0005 | g0314 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19011 | hp2 | a0001 | c0001 | t0005 | g0308 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19012 | hp1 | a0001 | c0001 | t0005 | g0316 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19030 | hp1 | a0001 | c0001 | t0007 | g0203 | AFR | LWK | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | LWK | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | LWK | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0141 | AFR | LWK | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19054 | hp2 | a0001 | c0001 | t0005 | g0317 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19055 | hp1 | a0001 | c0001 | t0005 | g0323 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19055 | hp2 | a0001 | c0001 | t0006 | g0190 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0369 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19057 | hp2 | a0001 | c0001 | t0005 | g0313 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0360 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19067 | hp2 | a0001 | c0001 | t0004 | g0353 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0367 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19081 | hp1 | a0001 | c0001 | t0005 | g0310 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0344 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19085 | hp1 | a0001 | c0001 | t0006 | g0144 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19089 | hp2 | a0001 | c0001 | t0004 | g0356 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19090 | hp2 | a0001 | c0001 | t0006 | g0161 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19091 | hp2 | a0001 | c0001 | t0006 | g0157 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0306 | AFR | YRI | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ASW | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ASW | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0292 | EUR | TSI | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0298 | EUR | TSI | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02109 | hp2 | a0001 | c0001 | t0019 | g0078 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0337 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0255 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0140 | AFR | MSL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | USA | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0339 | AFR | USA | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | USA | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | USA | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | LWK | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | LWK | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0100 | REF | REF | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0020 | g0221 | REF | REF | RABGEF1_chr7_66735733_66816464 | RABGEF1 | chr7 | 66735733 | 66816464 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:66805218
|
A | G | 1 | a0002 | 2 | HG02970.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.899A>G | p.Asn300Ser | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/9 | 976/3733 | 899/1476 | 300/491 | chr7 | 66805218 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:66771941
|
A | G | 1 | a0001c0004 | 1 | HG02040.hp1 | synonymous_variant | LOW | c.42A>G | p.Gln14Gln | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/9 | 119/3733 | 42/1476 | 14/491 | chr7 | 66771941 | ||
| chr7:66797390
|
C | T | 1 | a0001c0003 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.612C>T | p.Val204Val | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/9 | 689/3733 | 612/1476 | 204/491 | chr7 | 66797390 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:66809388
|
C | CAG | 22 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(19): Show | 399 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(396): Show |
3_prime_UTR_variant | MODIFIER | c.*105_*106dupAG | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 107 | INFO_REALIGN_3_PRIME | chr7 | 66809388 | ||||
| chr7:66809603
|
G | A | 1 | a0001c0001t0008 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*319G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 319 | chr7 | 66809603 | |||||
| chr7:66809885
|
C | G | 1 | a0001c0001t0019 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*601C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 601 | chr7 | 66809885 | |||||
| chr7:66809968
|
G | A | 5 | a0001c0001t0002a0001c0001t0005a0001c0001t0008others(2): Show | 84 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*684G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 684 | chr7 | 66809968 | |||||
| chr7:66810064
|
C | T | 1 | a0001c0001t0018 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*780C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 780 | chr7 | 66810064 | |||||
| chr7:66810279
|
A | G | 1 | a0001c0001t0005 | 25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*995A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 995 | chr7 | 66810279 | |||||
| chr7:66810628
|
C | G | 1 | a0001c0001t0017 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1344C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 1344 | chr7 | 66810628 | |||||
| chr7:66810693
|
G | C | 1 | a0001c0001t0011 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1409G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 1409 | chr7 | 66810693 | |||||
| chr7:66810748
|
A | G | 1 | a0001c0001t0016 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1464A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 1464 | chr7 | 66810748 | |||||
| chr7:66810918
|
C | T | 1 | a0001c0001t0019 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1634C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 1634 | chr7 | 66810918 | |||||
| chr7:66810999
|
A | C | 1 | a0001c0001t0007 | 15 | HG01884.hp2 HG01891.hp1 HG02257.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1715A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 1715 | chr7 | 66810999 | |||||
| chr7:66811077
|
A | T | 1 | a0001c0001t0015 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1793A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 1793 | chr7 | 66811077 | |||||
| chr7:66811135
|
T | C | 1 | a0001c0001t0012 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1851T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 1851 | chr7 | 66811135 | |||||
| chr7:66811155
|
C | CT | 3 | a0001c0001t0002a0001c0001t0008a0001c0001t0009 | 58 | HG00280.hp1 HG00423.hp1 HG00642.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*1872dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 1873 | INFO_REALIGN_3_PRIME | chr7 | 66811155 | ||||
| chr7:66811155
|
C | CTTTACAC others(3): Show |
1 | a0001c0001t0010 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1872_*1873insTTAC others(6): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 1873 | INFO_REALIGN_3_PRIME | chr7 | 66811155 | ||||
| chr7:66811166
|
A | G | 1 | a0001c0001t0004 | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1882A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 1882 | chr7 | 66811166 | |||||
| chr7:66811230
|
T | C | 13 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(10): Show | 190 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*1946T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 1946 | chr7 | 66811230 | |||||
| chr7:66811325
|
G | C | 3 | a0001c0001t0002a0001c0001t0008a0001c0001t0010 | 58 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*2041G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 2041 | chr7 | 66811325 | |||||
| chr7:66811334
|
C | T | 1 | a0001c0001t0019 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2050C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 2050 | chr7 | 66811334 | |||||
| chr7:66811337
|
C | T | 1 | a0001c0001t0014 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2053C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 2053 | chr7 | 66811337 | |||||
| chr7:66811341
|
C | T | 2 | a0001c0001t0006a0001c0001t0013 | 22 | HG00408.hp2 HG01074.hp2 HG01099.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2057C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 2057 | chr7 | 66811341 | |||||
| chr7:66811445
|
A | G | 1 | a0001c0001t0013 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2161A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 9/9 | 2161 | chr7 | 66811445 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:66740807
|
G | A | 3 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021 | 3 | HG02145.hp2 HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-18+15G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66740807 | ||||||
| chr7:66740835
|
A | G | 2 | a0001c0001t0007g0374a0001c0001t0007g0375 | 2 | HG02280.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-18+43A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66740835 | ||||||
| chr7:66740901
|
C | G | 2 | a0001c0001t0004g0372a0001c0001t0004g0373 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-18+109C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66740901 | ||||||
| chr7:66740941
|
C | G | 10 | a0001c0001t0001g0005a0001c0001t0001g0363a0001c0001t0001g0364others(7): Show | 12 | HG00544.hp1 HG02015.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.-18+149C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66740941 | ||||||
| chr7:66740949
|
C | G | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-18+157C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66740949 | ||||||
| chr7:66741005
|
T | G | 2 | a0001c0001t0002g0006a0001c0001t0002g0022 | 3 | HG01255.hp2 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-18+213T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66741005 | ||||||
| chr7:66741077
|
C | T | 1 | a0001c0001t0001g0339 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-18+285C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66741077 | ||||||
| chr7:66741126
|
C | G | 1 | a0001c0001t0001g0338 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-18+334C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66741126 | ||||||
| chr7:66741130
|
C | G | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18+338C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66741130 | ||||||
| chr7:66741388
|
G | T | 1 | a0001c0001t0001g0336 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-18+596G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66741388 | ||||||
| chr7:66741534
|
C | T | 1 | a0001c0001t0002g0335 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-18+742C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66741534 | ||||||
| chr7:66741543
|
C | T | 2 | a0002c0002t0001g0333a0002c0002t0001g0334 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-18+751C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66741543 | ||||||
| chr7:66741672
|
C | T | 25 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0310others(22): Show | 25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.-18+880C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66741672 | ||||||
| chr7:66741769
|
T | C | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18+977T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66741769 | ||||||
| chr7:66741886
|
C | T | 1 | a0001c0001t0003g0307 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-18+1094C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66741886 | ||||||
| chr7:66741941
|
C | T | 2 | a0001c0001t0003g0305a0001c0001t0003g0306 | 2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-18+1149C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66741941 | ||||||
| chr7:66741978
|
T | TA | 236 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0075others(233): Show | 251 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.-18+1198dupA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66741978 | |||||
| chr7:66741978
|
T | TAA | 15 | a0001c0001t0001g0007a0001c0001t0001g0023a0001c0001t0001g0024others(12): Show | 16 | HG00609.hp2 HG00621.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.-18+1197_-18+1198d others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66741978 | |||||
| chr7:66741993
|
A | G | 1 | a0001c0001t0004g0337 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-18+1201A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66741993 | ||||||
| chr7:66741997
|
G | A | 1 | a0001c0001t0004g0337 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-18+1205G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66741997 | ||||||
| chr7:66742099
|
C | T | 2 | a0001c0001t0005g0330a0001c0001t0005g0331 | 2 | NA18939.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-18+1307C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66742099 | ||||||
| chr7:66742150
|
C | CA | 153 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(150): Show | 161 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.-18+1368dupA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66742150 | |||||
| chr7:66742150
|
C | CAA | 47 | a0001c0001t0001g0075a0001c0001t0002g0001a0001c0001t0002g0006others(44): Show | 54 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.-18+1367_-18+1368d others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66742150 | |||||
| chr7:66742161
|
C | A | 253 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(250): Show | 269 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.-18+1369C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66742161 | ||||||
| chr7:66742259
|
G | A | 51 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(48): Show | 58 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.-18+1467G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66742259 | ||||||
| chr7:66742380
|
A | G | 148 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(145): Show | 156 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.-18+1588A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66742380 | ||||||
| chr7:66742493
|
A | G | 1 | a0001c0001t0001g0339 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-18+1701A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66742493 | ||||||
| chr7:66742527
|
C | G | 1 | a0001c0001t0001g0200 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-18+1735C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66742527 | ||||||
| chr7:66742705
|
G | C | 253 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(250): Show | 269 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.-18+1913G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66742705 | ||||||
| chr7:66742714
|
C | A | 2 | a0001c0001t0002g0035a0001c0001t0002g0036 | 2 | NA18955.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-18+1922C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66742714 | ||||||
| chr7:66742768
|
A | G | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | HG02155.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-18+1976A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66742768 | ||||||
| chr7:66742852
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-18+2060C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66742852 | ||||||
| chr7:66742897
|
G | C | 1 | a0001c0001t0019g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-18+2105G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66742897 | ||||||
| chr7:66743019
|
G | A | 1 | a0001c0001t0008g0076 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-18+2227G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66743019 | ||||||
| chr7:66743080
|
C | T | 1 | a0001c0001t0007g0304 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-18+2288C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66743080 | ||||||
| chr7:66743169
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-18+2377G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66743169 | ||||||
| chr7:66743189
|
G | A | 2 | a0002c0002t0001g0333a0002c0002t0001g0334 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-18+2397G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66743189 | ||||||
| chr7:66743197
|
C | T | 1 | a0001c0001t0001g0303 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-18+2405C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66743197 | ||||||
| chr7:66743198
|
T | A | 1 | a0001c0001t0003g0080 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-18+2406T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66743198 | ||||||
| chr7:66743325
|
AT | A | 6 | a0001c0001t0001g0194a0001c0001t0003g0195a0001c0001t0003g0196others(3): Show | 6 | HG01517.hp2 HG03195.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+2536delT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66743325 | |||||
| chr7:66743327
|
T | TA | 11 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(8): Show | 12 | HG02145.hp2 HG02280.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-18+2535_-18+2536i others(3): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66743327 | ||||||
| chr7:66743327
|
T | TAA | 44 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(41): Show | 51 | HG00280.hp1 HG00423.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.-18+2535_-18+2536i others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66743327 | ||||||
| chr7:66743328
|
T | A | 253 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(250): Show | 270 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.-18+2536T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66743328 | ||||||
| chr7:66743359
|
C | T | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18+2567C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66743359 | ||||||
| chr7:66743540
|
C | T | 50 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(47): Show | 57 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.-18+2748C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66743540 | ||||||
| chr7:66743647
|
G | C | 1 | a0001c0001t0001g0081 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-18+2855G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66743647 | ||||||
| chr7:66743798
|
G | A | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18+3006G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66743798 | ||||||
| chr7:66743918
|
A | G | 2 | a0001c0001t0001g0193a0001c0001t0001g0339 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-18+3126A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66743918 | ||||||
| chr7:66743968
|
G | T | 1 | a0001c0001t0001g0339 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-18+3176G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66743968 | ||||||
| chr7:66744021
|
TTTTTC | T | 51 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(48): Show | 55 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.-18+3249_-18+3253d others(7): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66744021 | |||||
| chr7:66744070
|
A | C | 253 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(250): Show | 269 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.-18+3278A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744070 | ||||||
| chr7:66744082
|
G | A | 1 | a0001c0001t0004g0337 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-18+3290G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744082 | ||||||
| chr7:66744092
|
A | T | 1 | a0001c0001t0001g0302 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-18+3300A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744092 | ||||||
| chr7:66744110
|
A | G | 2 | a0001c0001t0001g0300a0001c0001t0001g0301 | 2 | HG01099.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.-18+3318A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744110 | ||||||
| chr7:66744147
|
T | A | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-18+3355T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744147 | ||||||
| chr7:66744190
|
C | T | 26 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0310others(23): Show | 26 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.-18+3398C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744190 | ||||||
| chr7:66744193
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0202a0001c0001t0001g0207 | 4 | HG01109.hp1 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+3401G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744193 | ||||||
| chr7:66744200
|
C | T | 3 | a0001c0001t0004g0360a0001c0001t0004g0361a0001c0001t0004g0362 | 3 | NA18612.hp2 NA18959.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-18+3408C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744200 | ||||||
| chr7:66744266
|
C | T | 146 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(143): Show | 154 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.-18+3474C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744266 | ||||||
| chr7:66744283
|
C | T | 4 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0002g0071others(1): Show | 4 | NA18960.hp2 NA18980.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+3491C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744283 | ||||||
| chr7:66744324
|
G | T | 1 | a0001c0001t0001g0256 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-18+3532G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744324 | ||||||
| chr7:66744444
|
G | A | 4 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(1): Show | 4 | HG02109.hp1 HG02647.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+3652G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744444 | ||||||
| chr7:66744536
|
C | T | 1 | a0001c0001t0003g0192 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-18+3744C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744536 | ||||||
| chr7:66744590
|
C | G | 1 | a0001c0001t0019g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-18+3798C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744590 | ||||||
| chr7:66744667
|
C | CA | 63 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0023others(60): Show | 67 | HG00609.hp1 HG00621.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.-18+3895dupA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66744667 | |||||
| chr7:66744667
|
C | CAA | 6 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0004g0340others(3): Show | 6 | HG00642.hp2 HG02080.hp1 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+3894_-18+3895d others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66744667 | |||||
| chr7:66744667
|
CA | C | 72 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0299others(69): Show | 79 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.-18+3895delA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66744667 | |||||
| chr7:66744667
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0009g0201 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-18+3886_-18+3895d others(12): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66744667 | |||||
| chr7:66744697
|
C | T | 15 | a0001c0001t0001g0213a0001c0001t0007g0203a0001c0001t0007g0246others(12): Show | 15 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-18+3905C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744697 | ||||||
| chr7:66744749
|
T | C | 2 | a0001c0001t0003g0080a0001c0001t0011g0085 | 2 | HG02615.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-18+3957T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744749 | ||||||
| chr7:66744807
|
A | G | 1 | a0001c0001t0001g0245 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-18+4015A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744807 | ||||||
| chr7:66744912
|
G | T | 1 | a0001c0001t0009g0201 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-18+4120G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744912 | ||||||
| chr7:66744915
|
G | T | 25 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0310others(22): Show | 25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.-18+4123G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66744915 | ||||||
| chr7:66745020
|
A | G | 253 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(250): Show | 269 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.-18+4228A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66745020 | ||||||
| chr7:66745076
|
C | T | 2 | a0001c0001t0003g0305a0001c0001t0003g0306 | 2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-18+4284C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66745076 | ||||||
| chr7:66745109
|
G | A | 1 | a0001c0001t0007g0246 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-18+4317G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66745109 | ||||||
| chr7:66745191
|
C | CA | 28 | a0001c0001t0001g0214a0001c0001t0001g0285a0001c0001t0004g0018others(25): Show | 29 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.-18+4413dupA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66745191 | |||||
| chr7:66745208
|
A | T | 253 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(250): Show | 269 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.-18+4416A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66745208 | ||||||
| chr7:66745261
|
C | T | 5 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0002g0066others(2): Show | 5 | NA18941.hp1 NA18948.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+4469C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66745261 | ||||||
| chr7:66745376
|
A | G | 52 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(49): Show | 59 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.-18+4584A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66745376 | ||||||
| chr7:66745460
|
C | A | 3 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0216 | 3 | HG01261.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-18+4668C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66745460 | ||||||
| chr7:66745630
|
A | G | 2 | a0001c0001t0003g0305a0001c0001t0003g0306 | 2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-18+4838A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66745630 | ||||||
| chr7:66745663
|
G | C | 46 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(43): Show | 53 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.-18+4871G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66745663 | ||||||
| chr7:66745741
|
C | T | 1 | a0001c0001t0002g0063 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-18+4949C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66745741 | ||||||
| chr7:66745768
|
C | CA | 81 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(78): Show | 84 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.-18+4994dupA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66745768 | |||||
| chr7:66745768
|
C | CAAA | 24 | a0001c0001t0004g0018a0001c0001t0004g0341a0001c0001t0004g0342others(21): Show | 25 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.-18+4992_-18+4994d others(5): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66745768 | |||||
| chr7:66745768
|
CA | C | 58 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0003g0014others(55): Show | 60 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.-18+4994delA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66745768 | |||||
| chr7:66745843
|
C | G | 3 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021 | 3 | HG02145.hp2 HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-18+5051C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66745843 | ||||||
| chr7:66745905
|
A | T | 91 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(88): Show | 97 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.-18+5113A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66745905 | ||||||
| chr7:66746023
|
T | A | 253 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(250): Show | 269 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.-18+5231T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66746023 | ||||||
| chr7:66746106
|
T | C | 1 | a0001c0001t0009g0201 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-18+5314T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66746106 | ||||||
| chr7:66746207
|
T | A | 1 | a0001c0001t0001g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-18+5415T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66746207 | ||||||
| chr7:66746224
|
G | A | 4 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0198others(1): Show | 4 | HG02155.hp2 NA18612.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+5432G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66746224 | ||||||
| chr7:66746289
|
A | AT | 16 | a0001c0001t0001g0128a0001c0001t0001g0213a0001c0001t0007g0203others(13): Show | 16 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-18+5509dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66746289 | |||||
| chr7:66746410
|
C | G | 11 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0026others(8): Show | 11 | HG00609.hp2 HG00621.hp1 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18+5618C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66746410 | ||||||
| chr7:66746559
|
G | A | 1 | a0001c0001t0003g0142 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-18+5767G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66746559 | ||||||
| chr7:66746618
|
C | CT | 15 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(12): Show | 15 | HG00621.hp2 HG00741.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.-18+5848dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66746618 | |||||
| chr7:66746618
|
CT | C | 182 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(179): Show | 190 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.-18+5848delT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66746618 | |||||
| chr7:66746618
|
CTT | C | 8 | a0001c0001t0001g0079a0001c0001t0001g0088a0001c0001t0001g0089others(5): Show | 8 | HG01168.hp1 HG03942.hp1 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18+5847_-18+5848d others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66746618 | |||||
| chr7:66746781
|
G | A | 5 | a0001c0001t0001g0075a0001c0001t0001g0090a0001c0001t0001g0091others(2): Show | 5 | HG00438.hp1 NA18954.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+5989G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66746781 | ||||||
| chr7:66746784
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-18+5992C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66746784 | ||||||
| chr7:66746790
|
A | AT | 149 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 157 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.-18+6009dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66746790 | |||||
| chr7:66746941
|
G | GC | 91 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(88): Show | 97 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.-18+6150dupC | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66746941 | |||||
| chr7:66747138
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-18+6346G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66747138 | ||||||
| chr7:66747202
|
C | G | 1 | a0001c0001t0019g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-18+6410C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66747202 | ||||||
| chr7:66747226
|
C | T | 1 | a0001c0001t0007g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-18+6434C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66747226 | ||||||
| chr7:66747272
|
A | G | 1 | a0001c0001t0006g0183 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-18+6480A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66747272 | ||||||
| chr7:66747328
|
C | A | 4 | a0001c0001t0003g0129a0001c0001t0003g0145a0001c0001t0003g0146others(1): Show | 4 | HG03669.hp1 HG03710.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+6536C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66747328 | ||||||
| chr7:66747333
|
G | A | 4 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(1): Show | 4 | HG02109.hp1 HG02647.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+6541G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66747333 | ||||||
| chr7:66747437
|
T | A | 1 | a0001c0001t0003g0307 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-18+6645T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66747437 | ||||||
| chr7:66747523
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-18+6731A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66747523 | ||||||
| chr7:66747541
|
G | A | 25 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0310others(22): Show | 25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.-18+6749G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66747541 | ||||||
| chr7:66747610
|
G | A | 253 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(250): Show | 269 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.-18+6818G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66747610 | ||||||
| chr7:66747774
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-18+6982C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66747774 | ||||||
| chr7:66747819
|
C | T | 51 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(48): Show | 58 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.-18+7027C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66747819 | ||||||
| chr7:66747885
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-18+7093A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66747885 | ||||||
| chr7:66747900
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-18+7108T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66747900 | ||||||
| chr7:66747917
|
A | G | 1 | a0001c0001t0002g0059 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-18+7125A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66747917 | ||||||
| chr7:66748015
|
G | A | 1 | a0001c0001t0019g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-18+7223G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66748015 | ||||||
| chr7:66748121
|
C | T | 57 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(54): Show | 61 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.-18+7329C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66748121 | ||||||
| chr7:66748142
|
G | C | 1 | a0001c0001t0001g0279 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-18+7350G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66748142 | ||||||
| chr7:66748213
|
C | T | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-18+7421C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66748213 | ||||||
| chr7:66748504
|
G | A | 174 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(171): Show | 183 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.-18+7712G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66748504 | ||||||
| chr7:66748541
|
A | G | 1 | a0001c0003t0001g0124 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-18+7749A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66748541 | ||||||
| chr7:66749023
|
G | A | 251 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(248): Show | 267 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.-18+8231G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66749023 | ||||||
| chr7:66749262
|
C | T | 1 | a0001c0001t0002g0058 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-18+8470C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66749262 | ||||||
| chr7:66749358
|
A | C | 2 | a0001c0001t0007g0246a0001c0001t0007g0255 | 2 | HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-18+8566A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66749358 | ||||||
| chr7:66749367
|
T | G | 1 | a0001c0001t0001g0288 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-18+8575T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66749367 | ||||||
| chr7:66749390
|
G | C | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18+8598G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66749390 | ||||||
| chr7:66749580
|
C | T | 176 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(173): Show | 185 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.-18+8788C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66749580 | ||||||
| chr7:66749657
|
A | C | 1 | a0001c0001t0003g0146 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+8865A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66749657 | ||||||
| chr7:66749659
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-18+8867G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66749659 | ||||||
| chr7:66749710
|
A | G | 1 | a0001c0001t0005g0325 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-18+8918A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66749710 | ||||||
| chr7:66749746
|
C | A | 1 | a0001c0001t0001g0026 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-18+8954C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66749746 | ||||||
| chr7:66749788
|
A | G | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18+8996A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66749788 | ||||||
| chr7:66749798
|
C | T | 1 | a0001c0001t0004g0337 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-18+9006C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66749798 | ||||||
| chr7:66749819
|
A | T | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18+9027A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66749819 | ||||||
| chr7:66749861
|
C | A | 1 | a0001c0001t0001g0303 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-18+9069C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66749861 | ||||||
| chr7:66749946
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-18+9154C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66749946 | ||||||
| chr7:66750043
|
C | T | 1 | a0001c0001t0008g0076 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-18+9251C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66750043 | ||||||
| chr7:66750260
|
A | G | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG02602.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-18+9468A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66750260 | ||||||
| chr7:66750313
|
A | G | 77 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(74): Show | 84 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-18+9521A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66750313 | ||||||
| chr7:66750459
|
A | G | 1 | a0001c0001t0016g0296 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-18+9667A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66750459 | ||||||
| chr7:66750659
|
T | C | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-18+9867T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66750659 | ||||||
| chr7:66750727
|
G | A | 3 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021 | 3 | HG02145.hp2 HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-18+9935G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66750727 | ||||||
| chr7:66750963
|
T | A | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-18+10171T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66750963 | ||||||
| chr7:66751032
|
C | CT | 89 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0023others(86): Show | 94 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.-18+10254dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66751032 | |||||
| chr7:66751179
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-18+10387C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66751179 | ||||||
| chr7:66751185
|
C | T | 22 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(19): Show | 22 | HG00639.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-18+10393C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66751185 | ||||||
| chr7:66751206
|
T | G | 1 | a0001c0001t0001g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-18+10414T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66751206 | ||||||
| chr7:66751612
|
C | T | 1 | a0001c0001t0002g0072 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-18+10820C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66751612 | ||||||
| chr7:66751613
|
G | C | 1 | a0001c0001t0003g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-18+10821G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66751613 | ||||||
| chr7:66751640
|
C | G | 1 | a0001c0001t0001g0205 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-18+10848C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66751640 | ||||||
| chr7:66751700
|
C | G | 1 | a0001c0001t0004g0356 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-18+10908C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66751700 | ||||||
| chr7:66751742
|
A | G | 2 | a0001c0001t0003g0305a0001c0001t0003g0306 | 2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-18+10950A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66751742 | ||||||
| chr7:66751929
|
G | T | 5 | a0001c0001t0007g0252a0001c0001t0007g0253a0001c0001t0007g0254others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+11137G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66751929 | ||||||
| chr7:66751966
|
G | T | 1 | a0001c0001t0001g0122 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-18+11174G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66751966 | ||||||
| chr7:66751968
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-18+11176G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66751968 | ||||||
| chr7:66751993
|
T | TC | 25 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0310others(22): Show | 25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.-18+11202dupC | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66751993 | |||||
| chr7:66752108
|
A | G | 2 | a0001c0001t0003g0305a0001c0001t0003g0306 | 2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-18+11316A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66752108 | ||||||
| chr7:66752125
|
A | G | 251 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(248): Show | 267 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.-18+11333A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66752125 | ||||||
| chr7:66752195
|
TA | T | 51 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(48): Show | 58 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.-18+11414delA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66752195 | |||||
| chr7:66752196
|
A | T | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-18+11404A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66752196 | ||||||
| chr7:66752269
|
G | A | 1 | a0001c0001t0009g0201 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-18+11477G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66752269 | ||||||
| chr7:66752314
|
G | C | 1 | a0001c0001t0001g0198 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-18+11522G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66752314 | ||||||
| chr7:66752349
|
G | A | 2 | a0001c0001t0001g0364a0001c0001t0001g0365 | 2 | NA18951.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.-18+11557G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66752349 | ||||||
| chr7:66752474
|
A | G | 9 | a0001c0001t0003g0002a0001c0001t0003g0012a0001c0001t0003g0093others(6): Show | 12 | HG01243.hp2 HG02055.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-18+11682A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66752474 | ||||||
| chr7:66752493
|
T | TA | 29 | a0001c0001t0001g0079a0001c0001t0001g0276a0001c0001t0002g0042others(26): Show | 30 | HG00642.hp2 HG00735.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.-18+11716dupA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66752493 | |||||
| chr7:66752493
|
TA | T | 10 | a0001c0001t0001g0075a0001c0001t0001g0090a0001c0001t0001g0091others(7): Show | 10 | HG00438.hp1 HG01256.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18+11716delA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66752493 | |||||
| chr7:66752521
|
G | C | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-18+11729G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66752521 | ||||||
| chr7:66752632
|
A | G | 1 | a0001c0001t0003g0083 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-18+11840A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66752632 | ||||||
| chr7:66752676
|
A | G | 1 | a0001c0001t0002g0058 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-18+11884A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66752676 | ||||||
| chr7:66752787
|
A | G | 8 | a0001c0001t0001g0004a0001c0001t0001g0272a0001c0001t0001g0273others(5): Show | 10 | HG00741.hp1 HG01106.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18+11995A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66752787 | ||||||
| chr7:66752982
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-18+12190C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66752982 | ||||||
| chr7:66752983
|
T | C | 148 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(145): Show | 156 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.-18+12191T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66752983 | ||||||
| chr7:66753061
|
G | T | 1 | a0001c0001t0001g0241 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-18+12269G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66753061 | ||||||
| chr7:66753146
|
A | C | 1 | a0001c0001t0007g0251 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-18+12354A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66753146 | ||||||
| chr7:66753209
|
G | A | 147 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(144): Show | 155 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.-18+12417G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66753209 | ||||||
| chr7:66753234
|
T | A | 1 | a0001c0001t0004g0337 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-18+12442T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66753234 | ||||||
| chr7:66753365
|
A | T | 1 | a0001c0001t0007g0251 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-18+12573A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66753365 | ||||||
| chr7:66753623
|
C | G | 2 | a0001c0001t0002g0077a0001c0001t0019g0078 | 2 | HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-18+12831C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66753623 | ||||||
| chr7:66753692
|
T | A | 76 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(73): Show | 79 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.-18+12900T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66753692 | ||||||
| chr7:66753694
|
T | A | 76 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(73): Show | 79 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.-18+12902T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66753694 | ||||||
| chr7:66753700
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0004g0354 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-18+12908_-18+1290 others(16): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66753700 | ||||||
| chr7:66753701
|
G | GT | 41 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0205others(38): Show | 46 | HG00621.hp2 HG00639.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.-18+12932dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66753701 | |||||
| chr7:66753701
|
G | GTT | 52 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(49): Show | 55 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.-18+12931_-18+1293 others(6): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66753701 | |||||
| chr7:66753701
|
G | GTTT | 58 | a0001c0001t0001g0025a0001c0001t0001g0033a0001c0001t0001g0034others(55): Show | 59 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.-18+12930_-18+1293 others(7): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66753701 | |||||
| chr7:66753701
|
G | GTTTT | 25 | a0001c0001t0001g0081a0001c0001t0001g0084a0001c0001t0001g0087others(22): Show | 26 | HG00597.hp1 HG00738.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.-18+12929_-18+1293 others(8): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66753701 | |||||
| chr7:66753701
|
G | GTTTTT | 9 | a0001c0001t0003g0178a0001c0001t0003g0181a0001c0001t0003g0187others(6): Show | 9 | HG00735.hp2 HG01106.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18+12928_-18+1293 others(9): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66753701 | |||||
| chr7:66753701
|
G | GTTTTTT | 9 | a0001c0001t0005g0308a0001c0001t0005g0310a0001c0001t0005g0315others(6): Show | 9 | HG01928.hp1 HG02523.hp2 NA18939.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18+12927_-18+1293 others(10): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66753701 | |||||
| chr7:66753701
|
G | GTTTTTTT | 11 | a0001c0001t0005g0311a0001c0001t0005g0319a0001c0001t0005g0320others(8): Show | 11 | HG00438.hp2 HG01934.hp2 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18+12926_-18+1293 others(11): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66753701 | |||||
| chr7:66753701
|
G | GTTTTTTT others(3): Show |
2 | a0001c0001t0004g0361a0001c0001t0004g0372 | 2 | HG01515.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.-18+12923_-18+1293 others(14): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66753701 | |||||
| chr7:66753701
|
G | GTTTTTTT others(4): Show |
5 | a0001c0001t0004g0342a0001c0001t0004g0345a0001c0001t0004g0356others(2): Show | 5 | HG00642.hp2 HG01358.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+12922_-18+1293 others(15): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66753701 | |||||
| chr7:66753701
|
G | GTTTTTTT others(5): Show |
4 | a0001c0001t0004g0343a0001c0001t0004g0346a0001c0001t0004g0347others(1): Show | 4 | HG01257.hp2 HG02155.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+12921_-18+1293 others(16): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66753701 | |||||
| chr7:66753701
|
G | GTTTTTTT others(6): Show |
7 | a0001c0001t0004g0340a0001c0001t0004g0341a0001c0001t0004g0344others(4): Show | 7 | NA18939.hp1 NA18963.hp1 NA18980.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+12920_-18+1293 others(17): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66753701 | |||||
| chr7:66753701
|
G | GTTTTTTT others(7): Show |
4 | a0001c0001t0004g0018a0001c0001t0004g0352a0001c0001t0004g0353others(1): Show | 5 | NA18950.hp1 NA18953.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+12919_-18+1293 others(18): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66753701 | |||||
| chr7:66753701
|
G | GTTTTTTT others(8): Show |
3 | a0001c0001t0004g0355a0001c0001t0004g0357a0001c0001t0004g0359 | 3 | HG02165.hp1 HG02300.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-18+12918_-18+1293 others(19): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66753701 | |||||
| chr7:66753701
|
G | T | 1 | a0001c0001t0004g0354 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-18+12909G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66753701 | ||||||
| chr7:66753701
|
GT | G | 43 | a0001c0001t0001g0260a0001c0001t0001g0289a0001c0001t0002g0001others(40): Show | 50 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.-18+12932delT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66753701 | |||||
| chr7:66753832
|
G | T | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-18+13040G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66753832 | ||||||
| chr7:66753860
|
T | C | 268 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(265): Show | 284 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.-18+13068T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66753860 | ||||||
| chr7:66753895
|
TGGGGTTT others(290): Show |
T | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18+13111_-18+1340 others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66753895 | |||||
| chr7:66754005
|
A | AT | 9 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0217others(6): Show | 9 | HG01074.hp1 HG02056.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18+13228dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66754005 | |||||
| chr7:66754006
|
T | A | 25 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0310others(22): Show | 25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.-18+13214T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66754006 | ||||||
| chr7:66754012
|
T | C | 1 | a0001c0001t0003g0080 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-18+13220T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66754012 | ||||||
| chr7:66754192
|
C | T | 18 | a0001c0001t0001g0016a0001c0001t0001g0257a0001c0001t0001g0258others(15): Show | 19 | HG00609.hp1 HG00621.hp2 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.-18+13400C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66754192 | ||||||
| chr7:66754371
|
C | CT | 27 | a0001c0001t0003g0182a0001c0001t0004g0337a0001c0001t0005g0308others(24): Show | 27 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.-18+13594dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66754371 | |||||
| chr7:66754387
|
A | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-18+13595A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66754387 | ||||||
| chr7:66754399
|
C | T | 1 | a0001c0001t0002g0052 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-18+13607C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66754399 | ||||||
| chr7:66754507
|
G | A | 1 | a0001c0001t0003g0146 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+13715G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66754507 | ||||||
| chr7:66754554
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-18+13762G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66754554 | ||||||
| chr7:66754947
|
G | A | 25 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0310others(22): Show | 25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.-18+14155G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66754947 | ||||||
| chr7:66754973
|
G | A | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18+14181G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66754973 | ||||||
| chr7:66755293
|
CA | C | 370 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(367): Show | 395 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(392): Show |
intron_variant | MODIFIER | c.-18+14511delA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66755293 | |||||
| chr7:66755354
|
A | G | 1 | a0001c0001t0002g0022 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-18+14562A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66755354 | ||||||
| chr7:66755515
|
G | T | 53 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(50): Show | 57 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.-18+14723G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66755515 | ||||||
| chr7:66755821
|
C | T | 3 | a0001c0001t0002g0009a0001c0001t0002g0039a0001c0001t0002g0056 | 4 | NA18956.hp1 NA18971.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+15029C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66755821 | ||||||
| chr7:66755910
|
T | C | 4 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(1): Show | 4 | HG02109.hp1 HG02647.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+15118T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66755910 | ||||||
| chr7:66756005
|
G | A | 3 | a0001c0001t0005g0314a0001c0001t0005g0315a0001c0001t0005g0319 | 3 | HG01928.hp1 HG01934.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-18+15213G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66756005 | ||||||
| chr7:66756162
|
T | A | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18+15370T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66756162 | ||||||
| chr7:66756210
|
C | G | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18+15418C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66756210 | ||||||
| chr7:66756268
|
T | G | 3 | a0001c0001t0003g0129a0001c0001t0003g0145a0001c0001t0003g0184 | 3 | HG03669.hp1 HG03710.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-18+15476T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66756268 | ||||||
| chr7:66756273
|
G | A | 3 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021 | 3 | HG02145.hp2 HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-18+15481G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66756273 | ||||||
| chr7:66756425
|
C | G | 4 | a0001c0001t0003g0080a0001c0001t0003g0082a0001c0001t0003g0083others(1): Show | 4 | HG02615.hp2 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-15458C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66756425 | ||||||
| chr7:66756502
|
A | T | 50 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(47): Show | 57 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.-17-15381A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66756502 | ||||||
| chr7:66756505
|
T | C | 50 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(47): Show | 57 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.-17-15378T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66756505 | ||||||
| chr7:66756596
|
T | A | 1 | a0001c0001t0003g0182 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-17-15287T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66756596 | ||||||
| chr7:66756746
|
T | G | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-15137T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66756746 | ||||||
| chr7:66756956
|
G | A | 74 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(71): Show | 77 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.-17-14927G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66756956 | ||||||
| chr7:66757120
|
G | A | 2 | a0001c0001t0001g0222a0001c0001t0001g0223 | 2 | HG02922.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-17-14763G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66757120 | ||||||
| chr7:66757180
|
TTTTATGT others(3): Show |
T | 1 | a0001c0001t0001g0303 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-17-14700_-17-1469 others(14): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66757180 | |||||
| chr7:66757201
|
T | C | 1 | a0001c0001t0001g0303 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-17-14682T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66757201 | ||||||
| chr7:66757280
|
ATTGT | A | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-14600_-17-1459 others(8): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66757280 | |||||
| chr7:66757442
|
CAT | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0287 | 3 | HG01256.hp1 HG01258.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-17-14438_-17-1443 others(6): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66757442 | |||||
| chr7:66757547
|
A | G | 1 | a0001c0001t0002g0059 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-17-14336A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66757547 | ||||||
| chr7:66757813
|
G | A | 2 | a0001c0001t0003g0305a0001c0001t0003g0306 | 2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-17-14070G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66757813 | ||||||
| chr7:66757877
|
C | CTTTTTTT others(35): Show |
1 | a0001c0001t0001g0267 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-17-14005_-17-1400 others(46): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66757877 | |||||
| chr7:66757878
|
TGGGATTA others(35): Show |
T | 1 | a0001c0001t0001g0267 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-17-14004_-17-1396 others(46): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66757878 | ||||||
| chr7:66757891
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-17-13992G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66757891 | ||||||
| chr7:66757911
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-17-13972G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66757911 | ||||||
| chr7:66757920
|
A | AT | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-13954dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66757920 | |||||
| chr7:66758084
|
C | A | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-13799C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66758084 | ||||||
| chr7:66758085
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-17-13798C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66758085 | ||||||
| chr7:66758430
|
A | G | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-17-13453A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66758430 | ||||||
| chr7:66758432
|
T | C | 1 | a0001c0001t0004g0337 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-17-13451T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66758432 | ||||||
| chr7:66758474
|
T | C | 253 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(250): Show | 269 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.-17-13409T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66758474 | ||||||
| chr7:66758522
|
C | T | 1 | a0001c0001t0019g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-17-13361C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66758522 | ||||||
| chr7:66758597
|
G | A | 78 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(75): Show | 81 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.-17-13286G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66758597 | ||||||
| chr7:66758688
|
C | A | 2 | a0001c0001t0001g0212a0001c0001t0001g0224 | 2 | HG01071.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.-17-13195C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66758688 | ||||||
| chr7:66758701
|
T | C | 148 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(145): Show | 156 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.-17-13182T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66758701 | ||||||
| chr7:66758703
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-17-13180C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66758703 | ||||||
| chr7:66758705
|
G | GT | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-17-13177dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66758705 | |||||
| chr7:66758961
|
T | C | 2 | a0001c0001t0003g0148a0001c0001t0003g0182 | 2 | HG00423.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.-17-12922T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66758961 | ||||||
| chr7:66758985
|
G | T | 2 | a0001c0001t0001g0117a0001c0001t0001g0189 | 2 | NA19058.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-17-12898G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66758985 | ||||||
| chr7:66758990
|
A | G | 1 | a0001c0001t0019g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-17-12893A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66758990 | ||||||
| chr7:66759075
|
C | A | 1 | a0001c0001t0001g0089 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-17-12808C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66759075 | ||||||
| chr7:66759213
|
G | A | 1 | a0001c0001t0001g0366 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-17-12670G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66759213 | ||||||
| chr7:66759397
|
C | G | 1 | a0001c0001t0002g0071 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-17-12486C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66759397 | ||||||
| chr7:66759492
|
T | C | 1 | a0001c0001t0019g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-17-12391T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66759492 | ||||||
| chr7:66759494
|
G | T | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-17-12389G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66759494 | ||||||
| chr7:66759510
|
T | C | 176 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(173): Show | 185 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.-17-12373T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66759510 | ||||||
| chr7:66759519
|
A | T | 89 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(86): Show | 95 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.-17-12364A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66759519 | ||||||
| chr7:66759566
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-17-12317C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66759566 | ||||||
| chr7:66759704
|
A | G | 9 | a0001c0001t0001g0217a0001c0001t0001g0230a0001c0001t0001g0231others(6): Show | 9 | HG02257.hp2 HG02723.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.-17-12179A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66759704 | ||||||
| chr7:66759705
|
T | C | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-12178T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66759705 | ||||||
| chr7:66759724
|
A | T | 51 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(48): Show | 58 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.-17-12159A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66759724 | ||||||
| chr7:66759725
|
T | C | 51 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(48): Show | 58 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.-17-12158T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66759725 | ||||||
| chr7:66759771
|
T | G | 1 | a0001c0001t0004g0337 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-17-12112T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66759771 | ||||||
| chr7:66759822
|
G | A | 1 | a0001c0001t0004g0337 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-17-12061G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66759822 | ||||||
| chr7:66760109
|
C | T | 1 | a0001c0001t0001g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-17-11774C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66760109 | ||||||
| chr7:66760122
|
G | A | 1 | a0001c0001t0002g0077 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-17-11761G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66760122 | ||||||
| chr7:66760237
|
A | G | 1 | a0001c0001t0005g0318 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-17-11646A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66760237 | ||||||
| chr7:66760325
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-17-11558C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66760325 | ||||||
| chr7:66760442
|
A | AT | 57 | a0001c0001t0001g0031a0001c0001t0001g0109a0001c0001t0001g0125others(54): Show | 64 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.-17-11423dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66760442 | |||||
| chr7:66760442
|
A | ATTTTTT | 22 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(19): Show | 23 | HG00735.hp1 HG01257.hp2 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.-17-11428_-17-1142 others(10): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66760442 | |||||
| chr7:66760475
|
G | T | 1 | a0001c0001t0001g0245 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-17-11408G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66760475 | ||||||
| chr7:66760480
|
A | G | 1 | a0001c0001t0002g0072 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-17-11403A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66760480 | ||||||
| chr7:66760604
|
C | T | 1 | a0001c0001t0001g0266 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-17-11279C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66760604 | ||||||
| chr7:66760771
|
T | TC | 253 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(250): Show | 269 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.-17-11112_-17-1111 others(5): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66760771 | ||||||
| chr7:66760823
|
C | G | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-17-11060C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66760823 | ||||||
| chr7:66760852
|
C | T | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-17-11031C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66760852 | ||||||
| chr7:66760909
|
G | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0363a0001c0001t0001g0364others(7): Show | 12 | HG00544.hp1 HG02015.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.-17-10974G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66760909 | ||||||
| chr7:66761304
|
A | C | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-10579A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66761304 | ||||||
| chr7:66761389
|
G | T | 1 | a0001c0001t0004g0337 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-17-10494G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66761389 | ||||||
| chr7:66761452
|
G | A | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-10431G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66761452 | ||||||
| chr7:66761620
|
G | C | 8 | a0001c0001t0001g0005a0001c0001t0001g0363a0001c0001t0001g0364others(5): Show | 10 | HG00544.hp1 HG02015.hp1 NA18951.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-10263G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66761620 | ||||||
| chr7:66761633
|
C | T | 253 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(250): Show | 269 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.-17-10250C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66761633 | ||||||
| chr7:66761676
|
A | G | 1 | a0001c0001t0002g0059 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-17-10207A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66761676 | ||||||
| chr7:66761737
|
C | T | 1 | a0001c0001t0005g0313 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-17-10146C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66761737 | ||||||
| chr7:66761838
|
G | A | 46 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(43): Show | 53 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.-17-10045G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66761838 | ||||||
| chr7:66761848
|
C | G | 1 | a0001c0001t0001g0094 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-17-10035C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66761848 | ||||||
| chr7:66761890
|
A | G | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-9993A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66761890 | ||||||
| chr7:66761930
|
A | G | 4 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0198others(1): Show | 4 | HG02155.hp2 NA18612.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-9953A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66761930 | ||||||
| chr7:66761975
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-17-9908C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66761975 | ||||||
| chr7:66761982
|
T | C | 1 | a0001c0001t0005g0325 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-17-9901T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66761982 | ||||||
| chr7:66762063
|
C | A | 1 | a0001c0001t0001g0118 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-17-9820C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66762063 | ||||||
| chr7:66762064
|
A | C | 1 | a0001c0001t0001g0118 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-17-9819A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66762064 | ||||||
| chr7:66762083
|
CAT | C | 25 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0310others(22): Show | 25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.-17-9798_-17-9797d others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66762083 | |||||
| chr7:66762160
|
A | G | 1 | a0001c0001t0004g0337 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-17-9723A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66762160 | ||||||
| chr7:66762220
|
T | G | 1 | a0001c0001t0001g0111 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-17-9663T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66762220 | ||||||
| chr7:66762495
|
C | T | 147 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(144): Show | 155 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.-17-9388C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66762495 | ||||||
| chr7:66762718
|
A | T | 1 | a0001c0001t0004g0337 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-17-9165A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66762718 | ||||||
| chr7:66762723
|
C | T | 1 | a0001c0001t0004g0337 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-17-9160C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66762723 | ||||||
| chr7:66762801
|
C | T | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-9082C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66762801 | ||||||
| chr7:66762834
|
A | T | 1 | a0001c0001t0001g0118 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-17-9049A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66762834 | ||||||
| chr7:66763260
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-17-8623C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66763260 | ||||||
| chr7:66763267
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-17-8616C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66763267 | ||||||
| chr7:66763303
|
C | G | 77 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(74): Show | 84 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-17-8580C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66763303 | ||||||
| chr7:66763518
|
A | G | 9 | a0001c0001t0003g0002a0001c0001t0003g0012a0001c0001t0003g0093others(6): Show | 12 | HG01243.hp2 HG02055.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-17-8365A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66763518 | ||||||
| chr7:66763688
|
G | A | 1 | a0001c0001t0005g0313 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-17-8195G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66763688 | ||||||
| chr7:66763745
|
G | C | 253 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(250): Show | 269 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.-17-8138G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66763745 | ||||||
| chr7:66763746
|
T | G | 2 | a0002c0002t0001g0333a0002c0002t0001g0334 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-17-8137T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66763746 | ||||||
| chr7:66763811
|
A | C | 2 | a0001c0001t0001g0031a0001c0001t0001g0034 | 2 | HG00609.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.-17-8072A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66763811 | ||||||
| chr7:66763816
|
A | T | 1 | a0001c0001t0001g0118 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-17-8067A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66763816 | ||||||
| chr7:66763897
|
G | A | 1 | a0001c0001t0006g0149 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-17-7986G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66763897 | ||||||
| chr7:66764117
|
A | G | 2 | a0001c0001t0004g0357a0001c0001t0019g0078 | 2 | HG02109.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.-17-7766A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66764117 | ||||||
| chr7:66764245
|
A | G | 1 | a0001c0001t0001g0294 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-17-7638A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66764245 | ||||||
| chr7:66764249
|
T | C | 1 | a0001c0001t0001g0118 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-17-7634T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66764249 | ||||||
| chr7:66764252
|
C | G | 1 | a0001c0001t0006g0163 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-17-7631C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66764252 | ||||||
| chr7:66764275
|
A | G | 1 | a0001c0001t0002g0051 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-17-7608A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66764275 | ||||||
| chr7:66764322
|
T | TTTA | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-7558_-17-7556d others(5): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66764322 | |||||
| chr7:66764391
|
TG | T | 89 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(86): Show | 95 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.-17-7491delG | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66764391 | ||||||
| chr7:66764476
|
A | T | 1 | a0001c0001t0001g0086 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-17-7407A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66764476 | ||||||
| chr7:66764566
|
TCTGAGAG others(11): Show |
T | 1 | a0001c0001t0001g0118 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-17-7316_-17-7299d others(20): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66764566 | ||||||
| chr7:66764613
|
C | T | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-7270C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66764613 | ||||||
| chr7:66764648
|
T | C | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-17-7235T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66764648 | ||||||
| chr7:66764650
|
T | C | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-17-7233T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66764650 | ||||||
| chr7:66764885
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-17-6998T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66764885 | ||||||
| chr7:66764932
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-17-6951A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66764932 | ||||||
| chr7:66764948
|
A | C | 1 | a0001c0001t0001g0007 | 2 | NA20752.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-17-6935A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66764948 | ||||||
| chr7:66764951
|
T | C | 1 | a0001c0001t0009g0201 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-17-6932T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66764951 | ||||||
| chr7:66765008
|
C | A | 1 | a0001c0001t0012g0204 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-17-6875C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765008 | ||||||
| chr7:66765066
|
A | G | 57 | a0001c0001t0003g0014a0001c0001t0003g0129a0001c0001t0003g0130others(54): Show | 59 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.-17-6817A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765066 | ||||||
| chr7:66765159
|
T | C | 1 | a0001c0001t0001g0294 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-17-6724T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765159 | ||||||
| chr7:66765184
|
T | G | 253 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(250): Show | 269 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.-17-6699T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765184 | ||||||
| chr7:66765195
|
G | T | 1 | a0001c0001t0009g0201 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-17-6688G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765195 | ||||||
| chr7:66765315
|
C | G | 57 | a0001c0001t0003g0014a0001c0001t0003g0129a0001c0001t0003g0130others(54): Show | 59 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.-17-6568C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765315 | ||||||
| chr7:66765485
|
G | A | 63 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(60): Show | 68 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.-17-6398G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765485 | ||||||
| chr7:66765537
|
G | A | 89 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(86): Show | 95 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.-17-6346G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765537 | ||||||
| chr7:66765542
|
C | T | 149 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 157 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.-17-6341C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765542 | ||||||
| chr7:66765626
|
G | A | 1 | a0001c0001t0019g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-17-6257G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765626 | ||||||
| chr7:66765743
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-17-6140C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765743 | ||||||
| chr7:66765873
|
T | C | 176 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(173): Show | 185 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.-17-6010T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765873 | ||||||
| chr7:66765947
|
T | C | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-5936T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765947 | ||||||
| chr7:66765959
|
T | A | 1 | a0001c0001t0001g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-17-5924T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765959 | ||||||
| chr7:66765983
|
T | G | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-5900T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765983 | ||||||
| chr7:66765984
|
T | A | 30 | a0001c0001t0001g0003a0001c0001t0001g0222a0001c0001t0001g0223others(27): Show | 33 | HG00642.hp2 HG00735.hp1 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.-17-5899T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765984 | ||||||
| chr7:66765985
|
A | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0222a0001c0001t0001g0223 | 5 | HG01081.hp1 HG02451.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-5898A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66765985 | ||||||
| chr7:66766108
|
G | T | 1 | a0001c0001t0009g0201 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-17-5775G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66766108 | ||||||
| chr7:66766245
|
G | C | 3 | a0001c0001t0003g0082a0001c0001t0003g0083a0001c0001t0011g0085 | 3 | HG02615.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-17-5638G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66766245 | ||||||
| chr7:66766304
|
C | CA | 8 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0127others(5): Show | 8 | HG00738.hp2 HG01358.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17-5564dupA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66766304 | |||||
| chr7:66766304
|
CA | C | 30 | a0001c0001t0001g0239a0001c0001t0001g0301a0001c0001t0004g0018others(27): Show | 31 | HG00642.hp2 HG00735.hp1 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.-17-5564delA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66766304 | |||||
| chr7:66766420
|
G | C | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-17-5463G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66766420 | ||||||
| chr7:66766661
|
T | C | 374 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(371): Show | 399 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(396): Show |
intron_variant | MODIFIER | c.-17-5222T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66766661 | ||||||
| chr7:66766683
|
G | A | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-5200G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66766683 | ||||||
| chr7:66766710
|
C | CTTAT | 65 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0030others(62): Show | 66 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.-17-5146_-17-5143d others(6): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66766710 | |||||
| chr7:66766710
|
C | CTTATTTA others(1): Show |
69 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0023others(66): Show | 75 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-17-5150_-17-5143d others(10): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66766710 | |||||
| chr7:66766710
|
C | CTTATTTA others(5): Show |
19 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0031others(16): Show | 19 | HG00609.hp2 HG00735.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-17-5154_-17-5143d others(14): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66766710 | |||||
| chr7:66766710
|
CTTAT | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0222a0001c0001t0001g0223others(1): Show | 6 | HG01081.hp1 HG01106.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-5146_-17-5143d others(6): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66766710 | |||||
| chr7:66766808
|
T | A | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-17-5075T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66766808 | ||||||
| chr7:66766887
|
G | T | 1 | a0001c0001t0001g0126 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-17-4996G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66766887 | ||||||
| chr7:66767000
|
C | CT | 11 | a0001c0001t0001g0005a0001c0001t0001g0103a0001c0001t0001g0210others(8): Show | 13 | HG00544.hp1 HG02015.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.-17-4863dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66767000 | |||||
| chr7:66767000
|
CT | C | 197 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0023others(194): Show | 208 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.-17-4863delT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66767000 | |||||
| chr7:66767000
|
CTT | C | 35 | a0001c0001t0001g0026a0001c0001t0001g0105a0001c0001t0003g0002others(32): Show | 39 | HG00642.hp2 HG00735.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.-17-4864_-17-4863d others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66767000 | |||||
| chr7:66767005
|
T | C | 6 | a0001c0001t0001g0010a0001c0001t0001g0089a0001c0001t0001g0094others(3): Show | 7 | HG00280.hp2 HG01346.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-4878T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66767005 | ||||||
| chr7:66767015
|
T | A | 1 | a0001c0001t0006g0173 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-17-4868T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66767015 | ||||||
| chr7:66767059
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-17-4824A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66767059 | ||||||
| chr7:66767234
|
C | T | 1 | a0001c0001t0009g0201 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-17-4649C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66767234 | ||||||
| chr7:66767257
|
C | G | 1 | a0001c0001t0001g0302 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-17-4626C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66767257 | ||||||
| chr7:66767391
|
G | T | 1 | a0001c0001t0001g0302 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-17-4492G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66767391 | ||||||
| chr7:66767599
|
C | A | 2 | a0001c0001t0003g0130a0001c0001t0003g0152 | 2 | NA18973.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-17-4284C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66767599 | ||||||
| chr7:66767968
|
G | A | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-3915G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66767968 | ||||||
| chr7:66767978
|
G | A | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-3905G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66767978 | ||||||
| chr7:66767991
|
A | C | 1 | a0001c0001t0001g0096 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-17-3892A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66767991 | ||||||
| chr7:66768073
|
G | A | 57 | a0001c0001t0003g0014a0001c0001t0003g0129a0001c0001t0003g0130others(54): Show | 59 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.-17-3810G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66768073 | ||||||
| chr7:66768150
|
G | A | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-17-3733G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66768150 | ||||||
| chr7:66768166
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-17-3717G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66768166 | ||||||
| chr7:66768235
|
C | T | 51 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(48): Show | 58 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.-17-3648C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66768235 | ||||||
| chr7:66768292
|
G | A | 1 | a0001c0001t0004g0337 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-17-3591G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66768292 | ||||||
| chr7:66768302
|
C | G | 50 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(47): Show | 57 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.-17-3581C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66768302 | ||||||
| chr7:66768456
|
T | G | 1 | a0001c0001t0001g0366 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-17-3427T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66768456 | ||||||
| chr7:66768515
|
G | T | 1 | a0001c0001t0003g0178 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-3368G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66768515 | ||||||
| chr7:66768636
|
A | G | 149 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 157 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.-17-3247A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66768636 | ||||||
| chr7:66768647
|
TCTGAGAC | T | 3 | a0001c0001t0001g0212a0001c0001t0001g0218a0001c0001t0001g0224 | 3 | HG01071.hp1 HG01123.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-17-3232_-17-3226d others(9): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66768647 | |||||
| chr7:66768726
|
T | C | 1 | a0001c0001t0002g0072 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-17-3157T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66768726 | ||||||
| chr7:66769160
|
A | G | 1 | a0001c0001t0004g0357 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-17-2723A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66769160 | ||||||
| chr7:66769165
|
T | C | 3 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021 | 3 | HG02145.hp2 HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-17-2718T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66769165 | ||||||
| chr7:66769254
|
G | T | 1 | a0001c0001t0001g0132 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-17-2629G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66769254 | ||||||
| chr7:66769381
|
C | T | 2 | a0001c0001t0003g0156a0001c0001t0003g0172 | 2 | NA18952.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.-17-2502C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66769381 | ||||||
| chr7:66769424
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-17-2459C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66769424 | ||||||
| chr7:66769598
|
A | G | 21 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(18): Show | 21 | HG02055.hp2 HG02109.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.-17-2285A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66769598 | ||||||
| chr7:66769651
|
A | G | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-2232A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66769651 | ||||||
| chr7:66770140
|
T | A | 25 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0310others(22): Show | 25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.-17-1743T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66770140 | ||||||
| chr7:66770484
|
T | C | 4 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0216others(1): Show | 4 | HG01261.hp2 HG01517.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-1399T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66770484 | ||||||
| chr7:66770571
|
A | C | 1 | a0001c0001t0001g0293 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-17-1312A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66770571 | ||||||
| chr7:66770844
|
T | C | 2 | a0001c0001t0001g0232a0001c0001t0001g0256 | 2 | HG02451.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-17-1039T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66770844 | ||||||
| chr7:66770969
|
T | G | 1 | a0001c0001t0009g0201 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-17-914T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66770969 | ||||||
| chr7:66771048
|
T | C | 57 | a0001c0001t0003g0014a0001c0001t0003g0129a0001c0001t0003g0130others(54): Show | 59 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.-17-835T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66771048 | ||||||
| chr7:66771141
|
A | T | 77 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(74): Show | 84 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-17-742A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66771141 | ||||||
| chr7:66771207
|
T | C | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-17-676T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66771207 | ||||||
| chr7:66771284
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-17-599G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66771284 | ||||||
| chr7:66771392
|
G | A | 1 | a0001c0001t0002g0077 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-17-491G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66771392 | ||||||
| chr7:66771517
|
A | G | 1 | a0001c0001t0009g0201 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-17-366A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66771517 | ||||||
| chr7:66771556
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-17-327C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66771556 | ||||||
| chr7:66771620
|
G | T | 252 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(249): Show | 268 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.-17-263G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66771620 | ||||||
| chr7:66771632
|
AATTTTTT | A | 9 | a0001c0001t0003g0002a0001c0001t0003g0012a0001c0001t0003g0093others(6): Show | 12 | HG01243.hp2 HG02055.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-17-231_-17-225del others(7): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 66771632 | |||||
| chr7:66771781
|
A | C | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-17-102A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 1/8 | chr7 | 66771781 | ||||||
| chr7:66772114
|
C | T | 25 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0310others(22): Show | 25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.179+36C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66772114 | ||||||
| chr7:66772261
|
C | T | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.179+183C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66772261 | ||||||
| chr7:66772358
|
A | T | 1 | a0001c0001t0001g0202 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.179+280A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66772358 | ||||||
| chr7:66772422
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.179+344G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66772422 | ||||||
| chr7:66772454
|
A | AT | 16 | a0001c0001t0001g0213a0001c0001t0007g0203a0001c0001t0007g0228others(13): Show | 16 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.179+378dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 66772454 | |||||
| chr7:66772595
|
G | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0363a0001c0001t0001g0364others(7): Show | 12 | HG00544.hp1 HG02015.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.179+517G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66772595 | ||||||
| chr7:66772672
|
G | T | 1 | a0001c0001t0008g0076 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.179+594G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66772672 | ||||||
| chr7:66772738
|
C | T | 2 | a0001c0001t0002g0050a0001c0001t0002g0052 | 2 | NA18999.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.179+660C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66772738 | ||||||
| chr7:66772769
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0287a0001c0001t0004g0337 | 4 | HG01256.hp1 HG01258.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.179+691G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66772769 | ||||||
| chr7:66772913
|
A | G | 1 | a0001c0001t0002g0057 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.179+835A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66772913 | ||||||
| chr7:66772921
|
T | A | 213 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(210): Show | 226 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.179+843T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66772921 | ||||||
| chr7:66772924
|
A | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0102a0001c0001t0001g0121 | 4 | HG00597.hp2 HG02040.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.179+846A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66772924 | ||||||
| chr7:66772925
|
T | A | 71 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0024others(68): Show | 75 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.179+847T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66772925 | ||||||
| chr7:66772929
|
T | A | 1 | a0001c0001t0001g0338 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.179+851T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66772929 | ||||||
| chr7:66772971
|
A | T | 1 | a0001c0001t0002g0057 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.179+893A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66772971 | ||||||
| chr7:66773028
|
G | C | 1 | a0001c0001t0003g0080 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.179+950G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773028 | ||||||
| chr7:66773078
|
TG | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0094a0001c0001t0001g0104others(1): Show | 5 | HG00280.hp2 HG01346.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.179+1001delG | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773078 | ||||||
| chr7:66773081
|
TTG | T | 30 | a0001c0001t0002g0057a0001c0001t0002g0063a0001c0001t0004g0018others(27): Show | 31 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.179+1005_179+1006d others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 66773081 | |||||
| chr7:66773082
|
TG | T | 185 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0023others(182): Show | 199 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.179+1005delG | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773082 | ||||||
| chr7:66773083
|
G | T | 36 | a0001c0001t0001g0010a0001c0001t0001g0094a0001c0001t0001g0104others(33): Show | 37 | HG00280.hp2 HG00438.hp2 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.179+1005G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773083 | ||||||
| chr7:66773096
|
C | T | 147 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(144): Show | 155 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.179+1018C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773096 | ||||||
| chr7:66773115
|
TGTTGA | T | 51 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(48): Show | 58 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.179+1040_179+1044d others(7): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 66773115 | |||||
| chr7:66773209
|
A | T | 1 | a0001c0001t0001g0096 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.179+1131A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773209 | ||||||
| chr7:66773370
|
A | T | 5 | a0001c0001t0001g0099a0001c0001t0001g0109a0001c0001t0001g0194others(2): Show | 5 | HG00408.hp1 HG02083.hp1 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.179+1292A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773370 | ||||||
| chr7:66773395
|
G | A | 1 | a0001c0001t0003g0080 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.179+1317G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773395 | ||||||
| chr7:66773553
|
G | C | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.179+1475G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773553 | ||||||
| chr7:66773561
|
A | G | 77 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(74): Show | 84 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.179+1483A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773561 | ||||||
| chr7:66773566
|
A | G | 4 | a0001c0001t0001g0097a0001c0001t0001g0127a0001c0001t0001g0336others(1): Show | 4 | HG00738.hp2 HG01361.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.179+1488A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773566 | ||||||
| chr7:66773615
|
G | T | 1 | a0001c0001t0004g0337 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.179+1537G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773615 | ||||||
| chr7:66773734
|
C | A | 1 | a0001c0001t0003g0191 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.180-1493C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773734 | ||||||
| chr7:66773746
|
A | T | 1 | a0001c0001t0019g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.180-1481A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773746 | ||||||
| chr7:66773839
|
T | G | 3 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021 | 3 | HG02145.hp2 HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.180-1388T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773839 | ||||||
| chr7:66773912
|
C | T | 1 | a0001c0001t0003g0192 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.180-1315C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66773912 | ||||||
| chr7:66774142
|
C | A | 1 | a0001c0001t0019g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.180-1085C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66774142 | ||||||
| chr7:66774357
|
C | T | 77 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(74): Show | 84 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.180-870C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66774357 | ||||||
| chr7:66774392
|
C | G | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.180-835C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66774392 | ||||||
| chr7:66774399
|
G | C | 1 | a0001c0001t0001g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.180-828G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66774399 | ||||||
| chr7:66774601
|
T | G | 150 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(147): Show | 158 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.180-626T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66774601 | ||||||
| chr7:66774816
|
C | T | 57 | a0001c0001t0003g0014a0001c0001t0003g0129a0001c0001t0003g0130others(54): Show | 59 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.180-411C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66774816 | ||||||
| chr7:66774844
|
G | A | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.180-383G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66774844 | ||||||
| chr7:66774877
|
G | A | 4 | a0001c0001t0001g0097a0001c0001t0001g0127a0001c0001t0001g0336others(1): Show | 4 | HG00738.hp2 HG01361.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.180-350G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66774877 | ||||||
| chr7:66774975
|
A | T | 1 | a0001c0001t0009g0201 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.180-252A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66774975 | ||||||
| chr7:66775021
|
A | G | 177 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(174): Show | 186 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.180-206A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66775021 | ||||||
| chr7:66775197
|
A | G | 1 | a0001c0003t0001g0124 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.180-30A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66775197 | ||||||
| chr7:66775208
|
A | G | 1 | a0001c0003t0001g0124 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.180-19A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 2/8 | chr7 | 66775208 | ||||||
| chr7:66775402
|
C | G | 2 | a0001c0001t0002g0050a0001c0001t0002g0052 | 2 | NA18999.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.346+9C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66775402 | ||||||
| chr7:66775535
|
G | C | 8 | a0001c0001t0003g0014a0001c0001t0003g0165a0001c0001t0003g0166others(5): Show | 9 | HG00735.hp2 HG00738.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.346+142G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66775535 | ||||||
| chr7:66775536
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0287 | 3 | HG01256.hp1 HG01258.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.346+143G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66775536 | ||||||
| chr7:66775565
|
C | A | 1 | a0001c0001t0001g0234 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.346+172C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66775565 | ||||||
| chr7:66775652
|
C | A | 2 | a0001c0001t0003g0082a0001c0001t0003g0083 | 2 | HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.346+259C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66775652 | ||||||
| chr7:66775851
|
G | A | 77 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(74): Show | 84 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.346+458G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66775851 | ||||||
| chr7:66776005
|
T | G | 1 | a0001c0001t0002g0038 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.346+612T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66776005 | ||||||
| chr7:66776073
|
C | A | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.346+680C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66776073 | ||||||
| chr7:66776131
|
G | C | 1 | a0001c0001t0002g0050 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.346+738G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66776131 | ||||||
| chr7:66776263
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0102a0001c0001t0001g0121 | 4 | HG00597.hp2 HG02040.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.346+870G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66776263 | ||||||
| chr7:66776389
|
T | G | 25 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0310others(22): Show | 25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.346+996T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66776389 | ||||||
| chr7:66776461
|
G | A | 1 | a0001c0001t0019g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.346+1068G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66776461 | ||||||
| chr7:66776905
|
T | C | 1 | a0001c0001t0004g0337 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.346+1512T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66776905 | ||||||
| chr7:66776986
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.346+1593A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66776986 | ||||||
| chr7:66777189
|
G | A | 1 | a0001c0001t0002g0061 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.346+1796G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66777189 | ||||||
| chr7:66777429
|
G | A | 74 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(71): Show | 77 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.346+2036G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66777429 | ||||||
| chr7:66777606
|
A | G | 253 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(250): Show | 269 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.346+2213A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66777606 | ||||||
| chr7:66777644
|
C | T | 25 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0310others(22): Show | 25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.346+2251C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66777644 | ||||||
| chr7:66777660
|
C | G | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.346+2267C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66777660 | ||||||
| chr7:66777669
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.346+2276T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66777669 | ||||||
| chr7:66777675
|
C | T | 1 | a0001c0001t0019g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.346+2282C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66777675 | ||||||
| chr7:66777729
|
G | A | 3 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021 | 3 | HG02145.hp2 HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.346+2336G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66777729 | ||||||
| chr7:66777742
|
C | G | 253 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(250): Show | 269 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.346+2349C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66777742 | ||||||
| chr7:66777843
|
A | T | 2 | a0001c0001t0002g0041a0001c0001t0002g0048 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.346+2450A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66777843 | ||||||
| chr7:66777845
|
A | G | 1 | a0001c0001t0001g0299 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.346+2452A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66777845 | ||||||
| chr7:66777848
|
T | A | 50 | a0001c0001t0003g0014a0001c0001t0003g0130a0001c0001t0003g0131others(47): Show | 52 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.346+2455T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66777848 | ||||||
| chr7:66777883
|
C | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0363a0001c0001t0001g0364others(7): Show | 12 | HG00544.hp1 HG02015.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.346+2490C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66777883 | ||||||
| chr7:66777968
|
G | T | 1 | a0001c0001t0001g0237 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.346+2575G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66777968 | ||||||
| chr7:66778052
|
C | G | 26 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0310others(23): Show | 26 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.346+2659C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66778052 | ||||||
| chr7:66778276
|
G | GACAAATA others(8): Show |
25 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0310others(22): Show | 25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.346+2883_346+2884i others(17): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66778276 | ||||||
| chr7:66778280
|
G | C | 25 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0310others(22): Show | 25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.346+2887G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66778280 | ||||||
| chr7:66778281
|
G | T | 25 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0310others(22): Show | 25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.346+2888G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66778281 | ||||||
| chr7:66778282
|
T | A | 25 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0310others(22): Show | 25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.346+2889T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66778282 | ||||||
| chr7:66778386
|
G | A | 2 | a0001c0001t0001g0193a0001c0001t0001g0339 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.346+2993G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66778386 | ||||||
| chr7:66778401
|
A | C | 4 | a0001c0001t0003g0080a0001c0001t0003g0082a0001c0001t0003g0083others(1): Show | 4 | HG02615.hp2 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+3008A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66778401 | ||||||
| chr7:66778461
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.346+3068A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66778461 | ||||||
| chr7:66778684
|
G | T | 8 | a0001c0001t0003g0002a0001c0001t0003g0012a0001c0001t0003g0093others(5): Show | 11 | HG01243.hp2 HG02055.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.346+3291G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66778684 | ||||||
| chr7:66778775
|
G | A | 25 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0310others(22): Show | 25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.346+3382G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66778775 | ||||||
| chr7:66779234
|
G | A | 1 | a0001c0001t0001g0027 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.346+3841G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779234 | ||||||
| chr7:66779302
|
G | GAGACCAG others(7): Show |
5 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0236others(2): Show | 5 | HG02257.hp2 HG02723.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.346+3911_346+3924d others(16): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 66779302 | |||||
| chr7:66779322
|
G | A | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.346+3929G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779322 | ||||||
| chr7:66779350
|
A | G | 2 | a0002c0002t0001g0333a0002c0002t0001g0334 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.346+3957A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779350 | ||||||
| chr7:66779376
|
T | C | 1 | a0001c0001t0002g0057 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.346+3983T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779376 | ||||||
| chr7:66779408
|
G | T | 1 | a0001c0001t0008g0076 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.346+4015G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779408 | ||||||
| chr7:66779434
|
G | A | 5 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0115others(2): Show | 5 | HG00741.hp2 HG01192.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.346+4041G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779434 | ||||||
| chr7:66779436
|
G | A | 1 | a0001c0001t0004g0342 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.346+4043G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779436 | ||||||
| chr7:66779670
|
T | TA | 50 | a0001c0001t0001g0091a0001c0001t0001g0230a0001c0001t0001g0236others(47): Show | 57 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.347-3988dupA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 66779670 | |||||
| chr7:66779670
|
T | TAA | 6 | a0001c0001t0001g0231a0001c0001t0001g0237a0001c0001t0001g0240others(3): Show | 6 | HG02257.hp2 HG02723.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.347-3989_347-3988d others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 66779670 | |||||
| chr7:66779683
|
A | C | 1 | a0001c0001t0001g0227 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.347-3992A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779683 | ||||||
| chr7:66779690
|
C | G | 2 | a0001c0001t0001g0292a0001c0001t0001g0298 | 2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.347-3985C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779690 | ||||||
| chr7:66779720
|
G | A | 1 | a0001c0001t0003g0192 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.347-3955G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779720 | ||||||
| chr7:66779768
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.347-3907G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779768 | ||||||
| chr7:66779779
|
T | C | 57 | a0001c0001t0003g0014a0001c0001t0003g0129a0001c0001t0003g0130others(54): Show | 59 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.347-3896T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779779 | ||||||
| chr7:66779815
|
C | G | 2 | a0001c0001t0001g0232a0001c0001t0001g0256 | 2 | HG02451.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.347-3860C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779815 | ||||||
| chr7:66779827
|
G | A | 4 | a0001c0001t0003g0080a0001c0001t0003g0082a0001c0001t0003g0083others(1): Show | 4 | HG02615.hp2 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-3848G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779827 | ||||||
| chr7:66779829
|
A | C | 53 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(50): Show | 60 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.347-3846A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779829 | ||||||
| chr7:66779994
|
A | G | 77 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(74): Show | 80 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.347-3681A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66779994 | ||||||
| chr7:66780255
|
A | AC | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.347-3420_347-3419i others(3): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66780255 | ||||||
| chr7:66780299
|
G | A | 1 | a0001c0001t0001g0302 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.347-3376G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66780299 | ||||||
| chr7:66780314
|
T | C | 9 | a0001c0001t0003g0002a0001c0001t0003g0012a0001c0001t0003g0093others(6): Show | 12 | HG01243.hp2 HG02055.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.347-3361T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66780314 | ||||||
| chr7:66780414
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.347-3261T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66780414 | ||||||
| chr7:66780462
|
G | A | 1 | a0001c0001t0004g0337 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.347-3213G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66780462 | ||||||
| chr7:66780615
|
C | G | 1 | a0001c0001t0006g0180 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.347-3060C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66780615 | ||||||
| chr7:66780913
|
A | G | 57 | a0001c0001t0003g0014a0001c0001t0003g0129a0001c0001t0003g0130others(54): Show | 59 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.347-2762A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66780913 | ||||||
| chr7:66781193
|
G | C | 1 | a0001c0001t0001g0294 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.347-2482G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66781193 | ||||||
| chr7:66781487
|
T | G | 1 | a0001c0001t0002g0058 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.347-2188T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66781487 | ||||||
| chr7:66782128
|
C | T | 1 | a0001c0001t0002g0052 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.347-1547C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66782128 | ||||||
| chr7:66782189
|
T | C | 1 | a0001c0001t0003g0167 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.347-1486T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66782189 | ||||||
| chr7:66782274
|
T | G | 1 | a0001c0001t0002g0060 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.347-1401T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66782274 | ||||||
| chr7:66782290
|
T | C | 1 | a0001c0001t0001g0297 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.347-1385T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66782290 | ||||||
| chr7:66782346
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.347-1329A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66782346 | ||||||
| chr7:66782465
|
CT | C | 101 | a0001c0001t0001g0262a0001c0001t0002g0001a0001c0001t0002g0006others(98): Show | 109 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.347-1195delT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 66782465 | |||||
| chr7:66782493
|
G | A | 2 | a0001c0001t0007g0248a0001c0001t0007g0251 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.347-1182G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66782493 | ||||||
| chr7:66782520
|
G | A | 25 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(22): Show | 26 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.347-1155G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66782520 | ||||||
| chr7:66782602
|
G | A | 24 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0310others(21): Show | 24 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.347-1073G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66782602 | ||||||
| chr7:66782622
|
C | A | 1 | a0001c0001t0001g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.347-1053C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66782622 | ||||||
| chr7:66782700
|
C | T | 3 | a0001c0001t0001g0229a0001c0001t0001g0238a0001c0001t0001g0239 | 3 | HG02055.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.347-975C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66782700 | ||||||
| chr7:66782708
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.347-967C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66782708 | ||||||
| chr7:66782785
|
C | CA | 29 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(26): Show | 30 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.347-880dupA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 66782785 | |||||
| chr7:66782791
|
A | G | 2 | a0001c0001t0001g0222a0001c0001t0001g0223 | 2 | HG02922.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.347-884A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66782791 | ||||||
| chr7:66782840
|
T | C | 1 | a0001c0001t0009g0201 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.347-835T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66782840 | ||||||
| chr7:66782926
|
T | TGGTAGTT others(2760): Show |
1 | a0001c0001t0001g0224 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.347-732_347-731ins others(2767): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 66782926 | |||||
| chr7:66783024
|
G | T | 1 | a0001c0001t0002g0038 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.347-651G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66783024 | ||||||
| chr7:66783025
|
A | T | 1 | a0001c0001t0002g0038 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.347-650A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66783025 | ||||||
| chr7:66783067
|
C | T | 1 | a0001c0001t0007g0252 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.347-608C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66783067 | ||||||
| chr7:66783113
|
G | A | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.347-562G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66783113 | ||||||
| chr7:66783320
|
T | C | 1 | a0001c0001t0009g0201 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.347-355T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66783320 | ||||||
| chr7:66783395
|
T | C | 345 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(342): Show | 370 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.347-280T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66783395 | ||||||
| chr7:66783419
|
T | C | 1 | a0001c0001t0011g0085 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.347-256T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66783419 | ||||||
| chr7:66783463
|
A | G | 1 | a0001c0001t0001g0087 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.347-212A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66783463 | ||||||
| chr7:66783643
|
A | T | 9 | a0001c0001t0003g0002a0001c0001t0003g0012a0001c0001t0003g0093others(6): Show | 12 | HG01243.hp2 HG02055.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.347-32A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 3/8 | chr7 | 66783643 | ||||||
| chr7:66783870
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.513+29T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66783870 | ||||||
| chr7:66783921
|
C | A | 1 | a0001c0001t0002g0064 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.513+80C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66783921 | ||||||
| chr7:66784185
|
G | C | 2 | a0001c0001t0007g0203a0001c0001t0007g0228 | 2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.513+344G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66784185 | ||||||
| chr7:66784310
|
A | G | 1 | a0001c0001t0009g0201 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.513+469A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66784310 | ||||||
| chr7:66784623
|
G | T | 1 | a0001c0001t0008g0076 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.513+782G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66784623 | ||||||
| chr7:66784652
|
G | A | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.513+811G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66784652 | ||||||
| chr7:66784693
|
C | T | 1 | a0001c0001t0009g0201 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.513+852C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66784693 | ||||||
| chr7:66784694
|
A | G | 1 | a0001c0001t0009g0201 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.513+853A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66784694 | ||||||
| chr7:66785248
|
C | T | 51 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(48): Show | 58 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.513+1407C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66785248 | ||||||
| chr7:66785258
|
C | G | 1 | a0001c0001t0007g0304 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.513+1417C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66785258 | ||||||
| chr7:66785308
|
C | T | 1 | a0001c0001t0004g0337 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.513+1467C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66785308 | ||||||
| chr7:66785460
|
C | A | 1 | a0001c0001t0001g0278 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.513+1619C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66785460 | ||||||
| chr7:66785543
|
G | A | 3 | a0001c0001t0003g0082a0001c0001t0003g0083a0001c0001t0011g0085 | 3 | HG02615.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.513+1702G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66785543 | ||||||
| chr7:66785624
|
C | T | 1 | a0001c0001t0004g0337 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.513+1783C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66785624 | ||||||
| chr7:66785641
|
G | A | 1 | a0001c0001t0002g0061 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.513+1800G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66785641 | ||||||
| chr7:66785734
|
C | T | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.513+1893C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66785734 | ||||||
| chr7:66785743
|
A | G | 1 | a0001c0001t0001g0088 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.513+1902A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66785743 | ||||||
| chr7:66785746
|
C | T | 2 | a0001c0001t0005g0318a0001c0001t0006g0177 | 2 | NA18963.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.513+1905C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66785746 | ||||||
| chr7:66785857
|
G | A | 51 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(48): Show | 58 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.513+2016G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66785857 | ||||||
| chr7:66785872
|
TG | T | 74 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(71): Show | 77 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.513+2038delG | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66785872 | |||||
| chr7:66785878
|
G | GA | 3 | a0001c0001t0002g0054a0001c0001t0003g0093a0001c0001t0008g0076 | 3 | HG02055.hp1 HG03098.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.513+2037_513+2038i others(3): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66785878 | ||||||
| chr7:66785879
|
G | A | 152 | a0001c0001t0001g0120a0001c0001t0001g0193a0001c0001t0002g0001others(149): Show | 164 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.513+2038G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66785879 | ||||||
| chr7:66785879
|
GA | G | 19 | a0001c0001t0001g0207a0001c0001t0001g0213a0001c0001t0001g0225others(16): Show | 19 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.513+2049delA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66785879 | |||||
| chr7:66785882
|
A | G | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.513+2041A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66785882 | ||||||
| chr7:66785956
|
A | T | 1 | a0001c0001t0012g0204 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.513+2115A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66785956 | ||||||
| chr7:66786107
|
G | A | 25 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0310others(22): Show | 25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.513+2266G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66786107 | ||||||
| chr7:66786154
|
C | T | 1 | a0001c0001t0009g0201 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.513+2313C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66786154 | ||||||
| chr7:66786164
|
A | T | 2 | a0001c0001t0001g0258a0001c0001t0001g0270 | 2 | HG02080.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.513+2323A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66786164 | ||||||
| chr7:66786170
|
C | T | 1 | a0001c0001t0004g0337 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.513+2329C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66786170 | ||||||
| chr7:66786306
|
A | C | 1 | a0001c0001t0004g0359 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.513+2465A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66786306 | ||||||
| chr7:66786382
|
T | C | 77 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(74): Show | 84 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.513+2541T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66786382 | ||||||
| chr7:66786440
|
A | C | 1 | a0001c0001t0009g0201 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.513+2599A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66786440 | ||||||
| chr7:66786440
|
A | G | 1 | a0001c0001t0003g0195 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.513+2599A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66786440 | ||||||
| chr7:66786521
|
A | C | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.513+2680A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66786521 | ||||||
| chr7:66786693
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.513+2852C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66786693 | ||||||
| chr7:66786786
|
C | T | 105 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(102): Show | 113 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.513+2945C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66786786 | ||||||
| chr7:66786817
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.513+2976G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66786817 | ||||||
| chr7:66786821
|
T | C | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.513+2980T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66786821 | ||||||
| chr7:66787186
|
C | G | 1 | a0001c0001t0001g0286 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.513+3345C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66787186 | ||||||
| chr7:66787194
|
T | A | 3 | a0001c0001t0001g0229a0001c0001t0001g0238a0001c0001t0001g0239 | 3 | HG02055.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.513+3353T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66787194 | ||||||
| chr7:66787206
|
T | C | 1 | a0001c0001t0002g0335 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.513+3365T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66787206 | ||||||
| chr7:66787336
|
A | AT | 43 | a0001c0001t0001g0010a0001c0001t0001g0084a0001c0001t0001g0089others(40): Show | 45 | HG00280.hp2 HG00735.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.513+3520dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66787336 | |||||
| chr7:66787336
|
AT | A | 82 | a0001c0001t0001g0110a0001c0001t0001g0193a0001c0001t0001g0229others(79): Show | 90 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.513+3520delT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66787336 | |||||
| chr7:66787396
|
T | C | 1 | a0001c0001t0003g0145 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.513+3555T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66787396 | ||||||
| chr7:66787794
|
G | A | 1 | a0001c0001t0001g0339 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.513+3953G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66787794 | ||||||
| chr7:66787810
|
A | G | 1 | a0001c0001t0004g0356 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.513+3969A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66787810 | ||||||
| chr7:66788211
|
C | T | 51 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(48): Show | 58 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.513+4370C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66788211 | ||||||
| chr7:66788273
|
T | C | 1 | a0001c0001t0001g0087 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.513+4432T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66788273 | ||||||
| chr7:66788290
|
C | G | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.513+4449C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66788290 | ||||||
| chr7:66788453
|
C | CA | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.513+4618dupA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66788453 | |||||
| chr7:66788666
|
T | C | 1 | a0001c0001t0006g0158 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.513+4825T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66788666 | ||||||
| chr7:66788736
|
T | C | 1 | a0001c0001t0004g0337 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.513+4895T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66788736 | ||||||
| chr7:66788780
|
C | G | 2 | a0001c0001t0003g0305a0001c0001t0003g0306 | 2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.513+4939C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66788780 | ||||||
| chr7:66788783
|
G | A | 25 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0310others(22): Show | 25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.513+4942G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66788783 | ||||||
| chr7:66788816
|
G | A | 1 | a0001c0001t0004g0359 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.513+4975G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66788816 | ||||||
| chr7:66788824
|
G | A | 1 | a0001c0001t0001g0279 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.513+4983G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66788824 | ||||||
| chr7:66788965
|
A | T | 29 | a0001c0001t0001g0079a0001c0001t0004g0018a0001c0001t0004g0337others(26): Show | 30 | HG00642.hp2 HG00735.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.513+5124A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66788965 | ||||||
| chr7:66788968
|
T | A | 1 | a0001c0001t0008g0076 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.513+5127T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66788968 | ||||||
| chr7:66789021
|
T | C | 1 | a0001c0001t0009g0201 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.513+5180T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66789021 | ||||||
| chr7:66789134
|
T | C | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.513+5293T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66789134 | ||||||
| chr7:66789303
|
G | A | 162 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(159): Show | 172 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.513+5462G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66789303 | ||||||
| chr7:66789614
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.513+5773C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66789614 | ||||||
| chr7:66789659
|
A | G | 267 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(264): Show | 283 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.513+5818A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66789659 | ||||||
| chr7:66789665
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.513+5824G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66789665 | ||||||
| chr7:66789682
|
C | CA | 62 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(59): Show | 67 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.514-5803dupA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66789682 | |||||
| chr7:66789682
|
C | CAA | 6 | a0001c0001t0001g0260a0001c0001t0001g0271a0001c0001t0001g0272others(3): Show | 6 | HG00609.hp1 HG00621.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.514-5804_514-5803d others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66789682 | |||||
| chr7:66789682
|
CA | C | 120 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(117): Show | 124 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.514-5803delA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66789682 | |||||
| chr7:66789682
|
CAA | C | 77 | a0001c0001t0001g0128a0001c0001t0003g0014a0001c0001t0003g0129others(74): Show | 80 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.514-5804_514-5803d others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66789682 | |||||
| chr7:66789682
|
CAAA | C | 6 | a0001c0001t0003g0155a0001c0001t0004g0343a0001c0001t0004g0350others(3): Show | 6 | HG00558.hp1 HG01515.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.514-5805_514-5803d others(5): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66789682 | |||||
| chr7:66789780
|
C | T | 56 | a0001c0001t0003g0014a0001c0001t0003g0129a0001c0001t0003g0130others(53): Show | 58 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.514-5731C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66789780 | ||||||
| chr7:66790251
|
G | A | 162 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(159): Show | 172 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.514-5260G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66790251 | ||||||
| chr7:66790265
|
G | C | 4 | a0001c0001t0003g0012a0001c0001t0003g0134a0001c0001t0003g0137others(1): Show | 5 | HG01243.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.514-5246G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66790265 | ||||||
| chr7:66790324
|
C | T | 2 | a0001c0001t0002g0050a0001c0001t0002g0052 | 2 | NA18999.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.514-5187C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66790324 | ||||||
| chr7:66790341
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.514-5170T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66790341 | ||||||
| chr7:66790343
|
G | A | 4 | a0001c0001t0001g0205a0001c0001t0001g0208a0001c0001t0001g0209others(1): Show | 4 | HG02109.hp1 HG02647.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.514-5168G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66790343 | ||||||
| chr7:66790464
|
T | G | 52 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(49): Show | 59 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.514-5047T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66790464 | ||||||
| chr7:66790659
|
G | C | 253 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(250): Show | 269 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.514-4852G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66790659 | ||||||
| chr7:66790872
|
T | C | 1 | a0001c0001t0004g0337 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.514-4639T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66790872 | ||||||
| chr7:66790930
|
A | G | 6 | a0001c0001t0001g0016a0001c0001t0001g0257a0001c0001t0001g0262others(3): Show | 7 | HG02083.hp2 HG02129.hp2 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.514-4581A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66790930 | ||||||
| chr7:66791159
|
G | C | 1 | a0001c0001t0004g0337 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.514-4352G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66791159 | ||||||
| chr7:66791433
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.514-4078C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66791433 | ||||||
| chr7:66791964
|
T | G | 1 | a0001c0001t0001g0268 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.514-3547T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66791964 | ||||||
| chr7:66792068
|
C | G | 1 | a0001c0001t0002g0069 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.514-3443C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66792068 | ||||||
| chr7:66792069
|
G | T | 1 | a0001c0001t0002g0069 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.514-3442G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66792069 | ||||||
| chr7:66792070
|
C | T | 1 | a0001c0001t0002g0069 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.514-3441C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66792070 | ||||||
| chr7:66792072
|
A | T | 1 | a0001c0001t0002g0069 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.514-3439A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66792072 | ||||||
| chr7:66792110
|
CA | C | 55 | a0001c0001t0001g0087a0001c0001t0001g0098a0001c0001t0001g0120others(52): Show | 62 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.514-3385delA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66792110 | |||||
| chr7:66792110
|
CAA | C | 26 | a0001c0001t0002g0057a0001c0001t0005g0308a0001c0001t0005g0309others(23): Show | 26 | HG00438.hp2 HG01515.hp1 HG01928.hp1 others(23): Show |
intron_variant | MODIFIER | c.514-3386_514-3385d others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66792110 | |||||
| chr7:66792185
|
C | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0363a0001c0001t0001g0364others(7): Show | 12 | HG00544.hp1 HG02015.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.514-3326C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66792185 | ||||||
| chr7:66792194
|
C | T | 1 | a0001c0001t0007g0304 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.514-3317C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66792194 | ||||||
| chr7:66792537
|
G | A | 2 | a0001c0001t0003g0305a0001c0001t0003g0306 | 2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.514-2974G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66792537 | ||||||
| chr7:66792599
|
G | A | 4 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0216others(1): Show | 4 | HG01261.hp2 HG01517.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.514-2912G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66792599 | ||||||
| chr7:66792706
|
A | G | 1 | a0001c0001t0006g0162 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.514-2805A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66792706 | ||||||
| chr7:66792706
|
A | T | 1 | a0002c0002t0001g0334 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.514-2805A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66792706 | ||||||
| chr7:66792744
|
G | A | 1 | a0001c0001t0019g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.514-2767G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66792744 | ||||||
| chr7:66792760
|
C | T | 1 | a0001c0001t0003g0170 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.514-2751C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66792760 | ||||||
| chr7:66792942
|
G | A | 1 | a0001c0001t0004g0337 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.514-2569G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66792942 | ||||||
| chr7:66792974
|
G | A | 1 | a0001c0001t0003g0178 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.514-2537G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66792974 | ||||||
| chr7:66792997
|
CTG | C | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.514-2513_514-2512d others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66792997 | ||||||
| chr7:66793006
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.514-2505A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793006 | ||||||
| chr7:66793024
|
C | T | 25 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0310others(22): Show | 25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.514-2487C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793024 | ||||||
| chr7:66793093
|
G | A | 250 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(247): Show | 266 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.514-2418G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793093 | ||||||
| chr7:66793109
|
G | A | 1 | a0001c0001t0001g0007 | 2 | NA20752.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.514-2402G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793109 | ||||||
| chr7:66793123
|
A | C | 25 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0310others(22): Show | 25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.514-2388A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793123 | ||||||
| chr7:66793132
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.514-2379A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793132 | ||||||
| chr7:66793355
|
T | C | 1 | a0001c0001t0004g0337 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.514-2156T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793355 | ||||||
| chr7:66793478
|
A | G | 3 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021 | 3 | HG02145.hp2 HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.514-2033A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793478 | ||||||
| chr7:66793538
|
A | G | 1 | a0001c0001t0012g0204 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.514-1973A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793538 | ||||||
| chr7:66793679
|
G | GTACCTGC others(4588): Show |
1 | a0001c0001t0009g0201 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.514-1831_514-1830i others(4597): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | |||||
| chr7:66793679
|
G | GTACCTGC others(4579): Show |
1 | a0001c0001t0008g0076 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.514-1831_514-1830i others(4588): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | |||||
| chr7:66793679
|
G | GTACCTGC others(4588): Show |
1 | a0001c0001t0019g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.514-1831_514-1830i others(4597): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | |||||
| chr7:66793679
|
G | GTACCTGC others(4586): Show |
1 | a0001c0001t0005g0329 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.514-1831_514-1830i others(4595): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | |||||
| chr7:66793679
|
G | GTACCTGC others(4586): Show |
2 | a0001c0001t0005g0310a0001c0001t0005g0332 | 2 | NA18992.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.514-1831_514-1830i others(4595): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | |||||
| chr7:66793679
|
G | GTACCTGC others(4587): Show |
4 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.514-1831_514-1830i others(4596): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | |||||
| chr7:66793679
|
G | GTACCTGC others(4586): Show |
15 | a0001c0001t0005g0308a0001c0001t0005g0311a0001c0001t0005g0313others(12): Show | 15 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.514-1831_514-1830i others(4595): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | |||||
| chr7:66793679
|
G | GTACCTGC others(4588): Show |
1 | a0001c0001t0002g0050 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.514-1831_514-1830i others(4597): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | |||||
| chr7:66793679
|
G | GTACCTGC others(4587): Show |
45 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(42): Show | 52 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.514-1831_514-1830i others(4596): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | |||||
| chr7:66793679
|
G | GTACCTGC others(4587): Show |
1 | a0001c0001t0005g0309 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.514-1831_514-1830i others(4596): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | |||||
| chr7:66793679
|
G | GTACCTGC others(4586): Show |
5 | a0001c0001t0005g0312a0001c0001t0005g0321a0001c0001t0005g0323others(2): Show | 5 | NA18947.hp2 NA18970.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.514-1831_514-1830i others(4595): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | |||||
| chr7:66793679
|
G | GTACCTGC others(4585): Show |
1 | a0001c0001t0005g0324 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.514-1831_514-1830i others(4594): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | |||||
| chr7:66793679
|
G | GTACCTGC others(4589): Show |
1 | a0001c0001t0004g0355 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.514-1831_514-1830i others(4598): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | |||||
| chr7:66793679
|
G | GTACCTGC others(4588): Show |
21 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0342others(18): Show | 22 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.514-1831_514-1830i others(4597): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | |||||
| chr7:66793679
|
G | GTACCTGC others(4588): Show |
1 | a0001c0001t0004g0344 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.514-1831_514-1830i others(4597): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | |||||
| chr7:66793679
|
G | GTACCTGC others(4587): Show |
1 | a0001c0001t0004g0356 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.514-1831_514-1830i others(4596): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | |||||
| chr7:66793679
|
G | GTACCTGC others(4588): Show |
1 | a0001c0001t0004g0351 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.514-1831_514-1830i others(4597): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | |||||
| chr7:66793679
|
G | GTACCTGC others(4588): Show |
1 | a0001c0001t0004g0337 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.514-1831_514-1830i others(4597): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | |||||
| chr7:66793679
|
G | GTACCTGC others(4587): Show |
1 | a0001c0001t0004g0341 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.514-1831_514-1830i others(4596): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66793679 | |||||
| chr7:66793681
|
G | A | 1 | a0001c0001t0006g0174 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.514-1830G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793681 | ||||||
| chr7:66793684
|
T | C | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.514-1827T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793684 | ||||||
| chr7:66793734
|
AC | A | 8 | a0001c0001t0003g0002a0001c0001t0003g0012a0001c0001t0003g0093others(5): Show | 11 | HG01243.hp2 HG02055.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.514-1776delC | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793734 | ||||||
| chr7:66793800
|
G | C | 1 | a0001c0001t0003g0148 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.514-1711G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793800 | ||||||
| chr7:66793801
|
T | A | 1 | a0001c0001t0003g0148 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.514-1710T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793801 | ||||||
| chr7:66793802
|
C | G | 1 | a0001c0001t0003g0148 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.514-1709C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793802 | ||||||
| chr7:66793803
|
C | G | 1 | a0001c0001t0003g0148 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.514-1708C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793803 | ||||||
| chr7:66793805
|
G | A | 1 | a0001c0001t0003g0148 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.514-1706G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793805 | ||||||
| chr7:66793806
|
C | A | 1 | a0001c0001t0003g0148 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.514-1705C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793806 | ||||||
| chr7:66793817
|
G | C | 1 | a0001c0001t0019g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.514-1694G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793817 | ||||||
| chr7:66793874
|
C | T | 4 | a0001c0001t0001g0097a0001c0001t0001g0127a0001c0001t0001g0336others(1): Show | 4 | HG00738.hp2 HG01361.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.514-1637C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793874 | ||||||
| chr7:66793903
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0222a0001c0001t0001g0223 | 5 | HG01081.hp1 HG02451.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.514-1608A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66793903 | ||||||
| chr7:66794015
|
C | T | 2 | a0001c0001t0003g0305a0001c0001t0003g0306 | 2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.514-1496C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66794015 | ||||||
| chr7:66794039
|
A | T | 1 | a0001c0001t0019g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.514-1472A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66794039 | ||||||
| chr7:66794060
|
A | G | 1 | a0001c0001t0002g0077 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.514-1451A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66794060 | ||||||
| chr7:66794207
|
A | AT | 16 | a0001c0001t0001g0211a0001c0001t0001g0219a0001c0001t0001g0229others(13): Show | 16 | HG01952.hp1 HG01978.hp2 HG02897.hp1 others(13): Show |
intron_variant | MODIFIER | c.514-1279dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66794207 | |||||
| chr7:66794207
|
AT | A | 101 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(98): Show | 106 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.514-1279delT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66794207 | |||||
| chr7:66794207
|
ATT | A | 71 | a0001c0001t0001g0023a0001c0001t0001g0106a0001c0001t0001g0123others(68): Show | 79 | HG00280.hp1 HG00423.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.514-1280_514-1279d others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 66794207 | |||||
| chr7:66794234
|
C | T | 2 | a0001c0001t0007g0203a0001c0001t0007g0228 | 2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.514-1277C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66794234 | ||||||
| chr7:66794252
|
A | T | 6 | a0001c0001t0003g0080a0001c0001t0003g0082a0001c0001t0003g0083others(3): Show | 6 | HG02109.hp2 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.514-1259A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66794252 | ||||||
| chr7:66794258
|
T | A | 1 | a0001c0001t0019g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.514-1253T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66794258 | ||||||
| chr7:66794259
|
A | G | 51 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(48): Show | 58 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.514-1252A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66794259 | ||||||
| chr7:66794409
|
A | G | 1 | a0001c0001t0001g0295 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.514-1102A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66794409 | ||||||
| chr7:66794733
|
T | C | 1 | a0001c0001t0006g0157 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.514-778T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66794733 | ||||||
| chr7:66794746
|
C | T | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.514-765C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66794746 | ||||||
| chr7:66794967
|
C | T | 104 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(101): Show | 112 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.514-544C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66794967 | ||||||
| chr7:66795055
|
C | T | 1 | a0001c0001t0001g0007 | 2 | NA20752.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.514-456C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66795055 | ||||||
| chr7:66795109
|
C | T | 1 | a0001c0001t0001g0301 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.514-402C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66795109 | ||||||
| chr7:66795189
|
C | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0363a0001c0001t0001g0364others(7): Show | 12 | HG00544.hp1 HG02015.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.514-322C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66795189 | ||||||
| chr7:66795216
|
C | G | 2 | a0001c0001t0003g0156a0001c0001t0003g0172 | 2 | NA18952.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.514-295C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66795216 | ||||||
| chr7:66795302
|
A | G | 290 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(287): Show | 306 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.514-209A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66795302 | ||||||
| chr7:66795318
|
A | T | 1 | a0001c0001t0019g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.514-193A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66795318 | ||||||
| chr7:66795320
|
T | G | 1 | a0001c0001t0004g0337 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.514-191T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 4/8 | chr7 | 66795320 | ||||||
| chr7:66795835
|
G | A | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.595+243G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66795835 | ||||||
| chr7:66795937
|
G | C | 1 | a0001c0001t0001g0233 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.595+345G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66795937 | ||||||
| chr7:66795974
|
A | G | 57 | a0001c0001t0003g0014a0001c0001t0003g0129a0001c0001t0003g0130others(54): Show | 59 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.595+382A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66795974 | ||||||
| chr7:66796069
|
G | A | 4 | a0001c0001t0002g0006a0001c0001t0002g0022a0001c0001t0002g0037others(1): Show | 5 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.595+477G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66796069 | ||||||
| chr7:66796128
|
C | T | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.595+536C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66796128 | ||||||
| chr7:66796175
|
G | C | 57 | a0001c0001t0003g0014a0001c0001t0003g0129a0001c0001t0003g0130others(54): Show | 59 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.595+583G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66796175 | ||||||
| chr7:66796224
|
T | C | 2 | a0001c0001t0001g0222a0001c0001t0001g0223 | 2 | HG02922.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.595+632T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66796224 | ||||||
| chr7:66796228
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.595+636A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66796228 | ||||||
| chr7:66796238
|
T | TAA | 78 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(75): Show | 85 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.595+655_595+656dup others(2): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | 66796238 | |||||
| chr7:66796248
|
AG | A | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.595+657delG | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66796248 | ||||||
| chr7:66796351
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.595+759A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66796351 | ||||||
| chr7:66796382
|
A | G | 21 | a0001c0001t0001g0205a0001c0001t0001g0208a0001c0001t0001g0209others(18): Show | 21 | HG02055.hp2 HG02109.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.595+790A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66796382 | ||||||
| chr7:66796444
|
C | T | 5 | a0001c0001t0004g0342a0001c0001t0004g0345a0001c0001t0004g0354others(2): Show | 5 | HG00642.hp2 HG00735.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.595+852C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66796444 | ||||||
| chr7:66796531
|
G | A | 25 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0310others(22): Show | 25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.596-843G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66796531 | ||||||
| chr7:66796582
|
TTTTG | T | 6 | a0001c0001t0004g0343a0001c0001t0004g0344a0001c0001t0004g0350others(3): Show | 6 | NA18612.hp2 NA18959.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.596-772_596-769del others(4): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | 66796582 | |||||
| chr7:66796738
|
G | A | 1 | a0001c0001t0001g0368 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.596-636G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66796738 | ||||||
| chr7:66796828
|
C | T | 1 | a0001c0001t0004g0359 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.596-546C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66796828 | ||||||
| chr7:66796881
|
C | T | 1 | a0001c0001t0002g0070 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.596-493C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66796881 | ||||||
| chr7:66796907
|
T | C | 2 | a0001c0001t0001g0193a0001c0001t0001g0339 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.596-467T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66796907 | ||||||
| chr7:66796992
|
A | G | 1 | a0001c0001t0009g0201 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.596-382A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66796992 | ||||||
| chr7:66797229
|
A | G | 1 | a0001c0001t0001g0288 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.596-145A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66797229 | ||||||
| chr7:66797297
|
CTT | C | 162 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(159): Show | 172 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.596-75_596-74delTT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | 66797297 | |||||
| chr7:66797306
|
C | CA | 10 | a0001c0001t0001g0081a0001c0001t0001g0279a0001c0001t0002g0019others(7): Show | 10 | HG02074.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.596-53dupA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | 66797306 | |||||
| chr7:66797306
|
C | CAA | 44 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(41): Show | 51 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.596-54_596-53dupAA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | 66797306 | |||||
| chr7:66797321
|
AG | A | 34 | a0001c0001t0001g0095a0001c0001t0001g0100a0001c0001t0001g0105others(31): Show | 35 | HG00642.hp2 HG00735.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.596-52delG | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66797321 | ||||||
| chr7:66797322
|
G | A | 265 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(262): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.596-52G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66797322 | ||||||
| chr7:66797324
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0274a0001c0001t0001g0283 | 5 | HG00741.hp1 HG01346.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.596-50G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 5/8 | chr7 | 66797324 | ||||||
| chr7:66797528
|
C | T | 1 | a0001c0001t0003g0196 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.728+22C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66797528 | ||||||
| chr7:66797781
|
G | C | 3 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021 | 3 | HG02145.hp2 HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.728+275G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66797781 | ||||||
| chr7:66797839
|
G | A | 3 | a0001c0001t0004g0347a0001c0001t0004g0353a0001c0001t0004g0355 | 3 | HG01257.hp2 NA18994.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.728+333G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66797839 | ||||||
| chr7:66797986
|
G | A | 3 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021 | 3 | HG02145.hp2 HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.728+480G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66797986 | ||||||
| chr7:66798082
|
A | G | 2 | a0001c0001t0003g0305a0001c0001t0003g0306 | 2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.728+576A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66798082 | ||||||
| chr7:66798313
|
C | T | 1 | a0001c0001t0002g0077 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.728+807C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66798313 | ||||||
| chr7:66798357
|
AG | A | 25 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0310others(22): Show | 25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.728+855delG | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 66798357 | |||||
| chr7:66798414
|
C | T | 2 | a0001c0001t0001g0212a0001c0001t0001g0224 | 2 | HG01071.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.728+908C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66798414 | ||||||
| chr7:66798482
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.729-841G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66798482 | ||||||
| chr7:66798563
|
T | A | 173 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(170): Show | 186 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.729-760T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66798563 | ||||||
| chr7:66798576
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.729-747G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66798576 | ||||||
| chr7:66798797
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.729-526C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66798797 | ||||||
| chr7:66798861
|
C | A | 4 | a0001c0001t0001g0097a0001c0001t0001g0127a0001c0001t0001g0336others(1): Show | 4 | HG00738.hp2 HG01361.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.729-462C>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66798861 | ||||||
| chr7:66799007
|
C | T | 105 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(102): Show | 113 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.729-316C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66799007 | ||||||
| chr7:66799077
|
C | G | 1 | a0001c0001t0001g0126 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.729-246C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66799077 | ||||||
| chr7:66799123
|
A | G | 1 | a0001c0001t0006g0161 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.729-200A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66799123 | ||||||
| chr7:66799279
|
C | T | 2 | a0001c0001t0001g0232a0001c0001t0001g0256 | 2 | HG02451.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.729-44C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 6/8 | chr7 | 66799279 | ||||||
| chr7:66799492
|
A | G | 2 | a0001c0001t0001g0235a0001c0001t0001g0241 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.820+78A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66799492 | ||||||
| chr7:66799681
|
C | CT | 8 | a0001c0001t0001g0259a0001c0001t0005g0308a0001c0001t0005g0310others(5): Show | 8 | NA18939.hp2 NA18953.hp2 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.820+275dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 66799681 | |||||
| chr7:66800041
|
C | T | 77 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(74): Show | 84 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.820+627C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66800041 | ||||||
| chr7:66800263
|
A | G | 1 | a0001c0001t0005g0328 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.820+849A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66800263 | ||||||
| chr7:66800458
|
A | G | 105 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(102): Show | 113 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.820+1044A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66800458 | ||||||
| chr7:66800560
|
G | A | 1 | a0001c0001t0019g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.820+1146G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66800560 | ||||||
| chr7:66800574
|
C | G | 1 | a0001c0001t0001g0297 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.820+1160C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66800574 | ||||||
| chr7:66800582
|
C | G | 2 | a0001c0001t0001g0369a0001c0001t0001g0371 | 2 | NA18957.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.820+1168C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66800582 | ||||||
| chr7:66800622
|
G | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0222a0001c0001t0001g0223 | 5 | HG01081.hp1 HG02451.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.820+1208G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66800622 | ||||||
| chr7:66800649
|
G | A | 4 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(1): Show | 4 | HG00621.hp1 HG02015.hp2 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.820+1235G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66800649 | ||||||
| chr7:66800745
|
C | T | 1 | a0001c0001t0001g0303 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.820+1331C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66800745 | ||||||
| chr7:66801203
|
T | C | 1 | a0001c0001t0001g0369 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.820+1789T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66801203 | ||||||
| chr7:66801247
|
TTTTTAAT others(9): Show |
T | 1 | a0001c0001t0003g0143 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.820+1835_820+1850d others(18): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 66801247 | |||||
| chr7:66801316
|
G | A | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.820+1902G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66801316 | ||||||
| chr7:66801678
|
C | T | 1 | a0001c0001t0009g0201 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.820+2264C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66801678 | ||||||
| chr7:66801795
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.820+2381T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66801795 | ||||||
| chr7:66801886
|
G | A | 77 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(74): Show | 84 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.820+2472G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66801886 | ||||||
| chr7:66801903
|
G | T | 1 | a0001c0001t0001g0200 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.820+2489G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66801903 | ||||||
| chr7:66801911
|
G | T | 105 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(102): Show | 113 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.820+2497G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66801911 | ||||||
| chr7:66801919
|
G | T | 166 | a0001c0001t0001g0193a0001c0001t0001g0339a0001c0001t0002g0001others(163): Show | 176 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.820+2505G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66801919 | ||||||
| chr7:66802056
|
C | T | 1 | a0001c0001t0004g0337 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.820+2642C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66802056 | ||||||
| chr7:66802152
|
C | G | 6 | a0001c0001t0001g0015a0001c0001t0001g0202a0001c0001t0001g0207others(3): Show | 7 | HG01071.hp1 HG01109.hp1 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.820+2738C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66802152 | ||||||
| chr7:66802197
|
A | C | 1 | a0001c0001t0003g0182 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.820+2783A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66802197 | ||||||
| chr7:66802307
|
A | G | 1 | a0001c0001t0019g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.821-2833A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66802307 | ||||||
| chr7:66802606
|
C | G | 1 | a0001c0001t0008g0076 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.821-2534C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66802606 | ||||||
| chr7:66802616
|
G | T | 51 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(48): Show | 58 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.821-2524G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66802616 | ||||||
| chr7:66802707
|
A | G | 1 | a0001c0001t0019g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.821-2433A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66802707 | ||||||
| chr7:66802726
|
A | C | 2 | a0001c0001t0007g0203a0001c0001t0007g0228 | 2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.821-2414A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66802726 | ||||||
| chr7:66802772
|
T | G | 1 | a0001c0001t0001g0258 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.821-2368T>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66802772 | ||||||
| chr7:66802874
|
A | C | 1 | a0001c0001t0001g0114 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.821-2266A>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66802874 | ||||||
| chr7:66803061
|
T | C | 1 | a0001c0001t0019g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.821-2079T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66803061 | ||||||
| chr7:66803075
|
G | A | 1 | a0001c0001t0003g0143 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.821-2065G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66803075 | ||||||
| chr7:66803143
|
A | G | 25 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0310others(22): Show | 25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.821-1997A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66803143 | ||||||
| chr7:66803254
|
G | A | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.821-1886G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66803254 | ||||||
| chr7:66803315
|
C | T | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.821-1825C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66803315 | ||||||
| chr7:66803347
|
A | G | 25 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0310others(22): Show | 25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.821-1793A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66803347 | ||||||
| chr7:66803431
|
T | C | 2 | a0001c0001t0001g0031a0001c0001t0001g0034 | 2 | HG00609.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.821-1709T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66803431 | ||||||
| chr7:66803580
|
A | G | 2 | a0001c0001t0001g0107a0001c0001t0001g0119 | 2 | HG03704.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.821-1560A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66803580 | ||||||
| chr7:66803686
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.821-1454C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66803686 | ||||||
| chr7:66803786
|
G | A | 1 | a0001c0001t0004g0357 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.821-1354G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66803786 | ||||||
| chr7:66803900
|
A | G | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.821-1240A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66803900 | ||||||
| chr7:66803917
|
T | A | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.821-1223T>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66803917 | ||||||
| chr7:66803962
|
C | T | 77 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(74): Show | 84 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.821-1178C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66803962 | ||||||
| chr7:66803985
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.821-1155A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66803985 | ||||||
| chr7:66804064
|
T | C | 56 | a0001c0001t0003g0014a0001c0001t0003g0129a0001c0001t0003g0130others(53): Show | 58 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.821-1076T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66804064 | ||||||
| chr7:66804086
|
A | AT | 9 | a0001c0001t0001g0107a0001c0001t0001g0207a0001c0001t0001g0226others(6): Show | 9 | HG02486.hp1 HG03704.hp1 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.821-1037dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 66804086 | |||||
| chr7:66804086
|
AT | A | 9 | a0001c0001t0001g0193a0001c0001t0001g0295a0001c0001t0002g0042others(6): Show | 11 | HG02055.hp1 HG02572.hp2 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.821-1037delT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 66804086 | |||||
| chr7:66804208
|
C | T | 1 | a0001c0001t0019g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.821-932C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66804208 | ||||||
| chr7:66804219
|
G | A | 1 | a0001c0001t0003g0146 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.821-921G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66804219 | ||||||
| chr7:66804293
|
A | G | 2 | a0001c0001t0005g0330a0001c0001t0005g0331 | 2 | NA18939.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.821-847A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66804293 | ||||||
| chr7:66804333
|
G | A | 1 | a0001c0001t0001g0368 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.821-807G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66804333 | ||||||
| chr7:66804402
|
T | C | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.821-738T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66804402 | ||||||
| chr7:66804604
|
G | C | 1 | a0001c0001t0004g0337 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.821-536G>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66804604 | ||||||
| chr7:66804738
|
G | GA | 11 | a0001c0001t0001g0087a0001c0001t0001g0214a0001c0001t0001g0288others(8): Show | 12 | HG00735.hp2 HG00738.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.821-384dupA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 66804738 | |||||
| chr7:66804738
|
GA | G | 84 | a0001c0001t0001g0133a0001c0001t0001g0219a0001c0001t0001g0230others(81): Show | 92 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.821-384delA | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 66804738 | |||||
| chr7:66804739
|
A | G | 1 | a0001c0001t0001g0233 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.821-401A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66804739 | ||||||
| chr7:66804756
|
AG | A | 24 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0310others(21): Show | 24 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.821-383delG | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66804756 | ||||||
| chr7:66804891
|
G | A | 25 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0310others(22): Show | 25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.821-249G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66804891 | ||||||
| chr7:66804902
|
G | A | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.821-238G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 7/8 | chr7 | 66804902 | ||||||
| chr7:66805399
|
G | A | 1 | a0001c0001t0006g0185 | 1 | HG03942.hp2 | splice_region_variant&intron_variant | LOW | c.1077+3G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66805399 | ||||||
| chr7:66805417
|
T | C | 1 | a0001c0001t0019g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1077+21T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66805417 | ||||||
| chr7:66805609
|
G | A | 8 | a0001c0001t0003g0014a0001c0001t0003g0165a0001c0001t0003g0166others(5): Show | 9 | HG00735.hp2 HG00738.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1077+213G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66805609 | ||||||
| chr7:66805708
|
G | A | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1077+312G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66805708 | ||||||
| chr7:66805711
|
T | C | 25 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0310others(22): Show | 25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.1077+315T>C | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66805711 | ||||||
| chr7:66805739
|
C | CTCAT | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.1077+351_1077+354d others(6): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr7 | 66805739 | |||||
| chr7:66805745
|
C | G | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0241 | 3 | HG02965.hp2 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1077+349C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66805745 | ||||||
| chr7:66805781
|
A | G | 25 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0310others(22): Show | 25 | HG00438.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.1077+385A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66805781 | ||||||
| chr7:66805911
|
A | AT | 12 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0222others(9): Show | 14 | HG01081.hp1 HG01943.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.1077+530dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr7 | 66805911 | |||||
| chr7:66805937
|
G | A | 3 | a0001c0001t0001g0230a0001c0001t0001g0237a0001c0001t0001g0240 | 3 | HG02257.hp2 HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1077+541G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66805937 | ||||||
| chr7:66806248
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1077+852G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66806248 | ||||||
| chr7:66806386
|
G | A | 3 | a0001c0001t0002g0008a0001c0001t0002g0035a0001c0001t0002g0036 | 4 | NA18955.hp1 NA19002.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.1077+990G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66806386 | ||||||
| chr7:66806419
|
C | T | 3 | a0001c0001t0001g0289a0001c0001t0001g0295a0001c0001t0001g0300 | 3 | HG01074.hp1 HG01099.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1077+1023C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66806419 | ||||||
| chr7:66806640
|
C | CT | 92 | a0001c0001t0001g0025a0001c0001t0001g0119a0001c0001t0001g0218others(89): Show | 102 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.1077+1265dupT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr7 | 66806640 | |||||
| chr7:66806640
|
C | CTT | 5 | a0001c0001t0002g0040a0001c0001t0002g0073a0001c0001t0004g0018others(2): Show | 6 | NA18953.hp1 NA18968.hp1 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.1077+1264_1077+126 others(6): Show |
RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr7 | 66806640 | |||||
| chr7:66806640
|
CT | C | 28 | a0001c0001t0001g0084a0001c0001t0001g0102a0001c0001t0001g0123others(25): Show | 28 | HG01123.hp1 HG01169.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1077+1265delT | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr7 | 66806640 | |||||
| chr7:66806827
|
A | G | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.1077+1431A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66806827 | ||||||
| chr7:66806897
|
G | A | 104 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(101): Show | 112 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1077+1501G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66806897 | ||||||
| chr7:66806922
|
G | T | 1 | a0001c0001t0001g0007 | 2 | NA20752.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1077+1526G>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66806922 | ||||||
| chr7:66806983
|
G | A | 4 | a0001c0001t0002g0009a0001c0001t0002g0039a0001c0001t0002g0044others(1): Show | 5 | NA18940.hp2 NA18956.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.1077+1587G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66806983 | ||||||
| chr7:66807034
|
C | G | 1 | a0001c0001t0003g0146 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1077+1638C>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66807034 | ||||||
| chr7:66807297
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1078-1589C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66807297 | ||||||
| chr7:66807441
|
G | A | 1 | a0001c0001t0003g0093 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1078-1445G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66807441 | ||||||
| chr7:66807517
|
C | T | 1 | a0001c0001t0002g0055 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1078-1369C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66807517 | ||||||
| chr7:66808134
|
A | T | 1 | a0001c0001t0004g0337 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1078-752A>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66808134 | ||||||
| chr7:66808145
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1078-741C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66808145 | ||||||
| chr7:66808234
|
C | T | 27 | a0001c0001t0004g0018a0001c0001t0004g0337a0001c0001t0004g0340others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.1078-652C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66808234 | ||||||
| chr7:66808332
|
C | T | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.1078-554C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66808332 | ||||||
| chr7:66808372
|
C | T | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | HG02155.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1078-514C>T | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66808372 | ||||||
| chr7:66808422
|
G | A | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.1078-464G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66808422 | ||||||
| chr7:66808504
|
G | A | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.1078-382G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66808504 | ||||||
| chr7:66808763
|
A | G | 1 | a0001c0001t0003g0131 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1078-123A>G | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66808763 | ||||||
| chr7:66808802
|
G | A | 26 | a0001c0001t0004g0018a0001c0001t0004g0340a0001c0001t0004g0341others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.1078-84G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66808802 | ||||||
| chr7:66808863
|
G | A | 1 | a0001c0001t0001g0297 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1078-23G>A | RABGEF1 | ENSG00000154710.18 | transcript | ENST00000284957.9 | protein_coding | 8/8 | chr7 | 66808863 |