| geneid | 5874 |
|---|---|
| ensemblid | ENSG00000041353.10 |
| hgncid | 9767 |
| symbol | RAB27B |
| name | RAB27B, member RAS oncogene family |
| refseq_nuc | NM_004163.4 |
| refseq_prot | NP_004154.2 |
| ensembl_nuc | ENST00000262094.10 |
| ensembl_prot | ENSP00000262094.4 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 54828477 |
| end | 54895516 |
| strand | + |
| ver | v1.2 |
| region | chr18:54828477-54895516 |
| region5000 | chr18:54823477-54900516 |
| regionname0 | RAB27B_chr18_54828477_54895516 |
| regionname5000 | RAB27B_chr18_54823477_54900516 |
| 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 | 218 | 331 | 81 | 74 | 126 | 8 | 40 | 102 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0002 | 0/0 | 218 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0003 | 0/0 | 218 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0004 | 0/0 | 218 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| 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 | 657 | 331 | 81 | 74 | 126 | 8 | 40 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| c0002 | 0/0 | 657 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| c0003 | 0/0 | 657 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| c0004 | 0/0 | 657 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| 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 | 6343 | 141 | 24 | 31 | 67 | 1 | 17 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0002 | 0/0 | 6343 | 66 | 2 | 15 | 38 | 1 | 10 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0003 | 0/0 | 6343 | 16 | 0 | 10 | 0 | 2 | 4 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0004 | 1/0 | 6347 | 13 | 12 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0005 | 0/0 | 6343 | 11 | 0 | 8 | 0 | 2 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0006 | 0/0 | 6343 | 9 | 8 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0007 | 0/0 | 6343 | 8 | 6 | 1 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0008 | 0/0 | 6343 | 8 | 8 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0009 | 0/0 | 6343 | 7 | 1 | 4 | 1 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0010 | 0/0 | 6342 | 7 | 3 | 0 | 4 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0011 | 0/0 | 6343 | 4 | 0 | 0 | 4 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0012 | 0/0 | 6343 | 4 | 0 | 0 | 4 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0013 | 0/0 | 6343 | 2 | 0 | 0 | 0 | 0 | 2 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0014 | 0/0 | 6343 | 2 | 0 | 0 | 0 | 0 | 2 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0015 | 0/0 | 6343 | 2 | 0 | 0 | 0 | 1 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0016 | 0/0 | 6343 | 2 | 2 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0017 | 0/0 | 6343 | 2 | 0 | 0 | 2 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0018 | 0/0 | 6184 | 2 | 2 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0019 | 0/0 | 6343 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0020 | 0/0 | 6343 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0021 | 0/0 | 6343 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0022 | 0/0 | 6343 | 1 | 0 | 0 | 0 | 1 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0023 | 0/0 | 6343 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0024 | 0/0 | 6347 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0025 | 0/0 | 6347 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0026 | 0/0 | 6347 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0027 | 0/0 | 6343 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0028 | 0/0 | 6343 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0029 | 0/0 | 6343 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0030 | 0/0 | 6342 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0031 | 0/0 | 6342 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0032 | 0/0 | 6343 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0033 | 0/0 | 6343 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0034 | 0/0 | 6343 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0035 | 0/0 | 6343 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0036 | 0/0 | 6343 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0037 | 0/0 | 6343 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0038 | 0/0 | 6343 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0039 | 0/0 | 6343 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0040 | 0/0 | 6343 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0041 | 0/0 | 6343 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0042 | 0/0 | 6343 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0043 | 0/0 | 6343 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0044 | 0/0 | 6343 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0045 | 0/0 | 6343 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| t0046 | 0/0 | 6347 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0008 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0136 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0306 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| 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 | 657 | 331 | 81 | 74 | 126 | 8 | 40 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0002c0004 | 0/0 | 657 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0003c0003 | 0/0 | 657 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0004c0002 | 0/0 | 657 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 6999 | 140 | 23 | 31 | 67 | 1 | 17 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0002 | 0/0 | 6999 | 66 | 2 | 15 | 38 | 1 | 10 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0003 | 0/0 | 6999 | 16 | 0 | 10 | 0 | 2 | 4 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0004 | 1/0 | 7003 | 13 | 12 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0005 | 0/0 | 6999 | 11 | 0 | 8 | 0 | 2 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0006 | 0/0 | 6999 | 9 | 8 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0007 | 0/0 | 6999 | 7 | 5 | 1 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0008 | 0/0 | 6999 | 8 | 8 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0009 | 0/0 | 6999 | 7 | 1 | 4 | 1 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0010 | 0/0 | 6998 | 7 | 3 | 0 | 4 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0011 | 0/0 | 6999 | 4 | 0 | 0 | 4 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0012 | 0/0 | 6999 | 4 | 0 | 0 | 4 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0013 | 0/0 | 6999 | 2 | 0 | 0 | 0 | 0 | 2 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0014 | 0/0 | 6999 | 2 | 0 | 0 | 0 | 0 | 2 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0015 | 0/0 | 6999 | 2 | 0 | 0 | 0 | 1 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0016 | 0/0 | 6999 | 2 | 2 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0017 | 0/0 | 6999 | 2 | 0 | 0 | 2 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0018 | 0/0 | 6840 | 2 | 2 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0019 | 0/0 | 6999 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0020 | 0/0 | 6999 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0021 | 0/0 | 6999 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0022 | 0/0 | 6999 | 1 | 0 | 0 | 0 | 1 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0023 | 0/0 | 6999 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0024 | 0/0 | 7003 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0025 | 0/0 | 7003 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0026 | 0/0 | 7003 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0027 | 0/0 | 6999 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0028 | 0/0 | 6999 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0029 | 0/0 | 6999 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0030 | 0/0 | 6998 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0032 | 0/0 | 6999 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0033 | 0/0 | 6999 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0034 | 0/0 | 6999 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0035 | 0/0 | 6999 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0036 | 0/0 | 6999 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0037 | 0/0 | 6999 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0038 | 0/0 | 6999 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0039 | 0/0 | 6999 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0040 | 0/0 | 6999 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0041 | 0/0 | 6999 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0042 | 0/0 | 6999 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0043 | 0/0 | 6999 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0044 | 0/0 | 6999 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0045 | 0/0 | 6999 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0001c0001t0046 | 0/0 | 7003 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0002c0004t0007 | 0/0 | 6999 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0003c0003t0031 | 0/0 | 6998 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| a0004c0002t0001 | 0/0 | 6999 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | copy fasta | chr18 | 54823477 | 54900516 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0136 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0003g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0004g0306 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0004g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0004g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0005g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0005g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0005g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0005g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0005g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0005g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0005g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0005g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0005g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0005g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0006g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0006g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0006g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0006g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0006g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0006g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0006g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0007g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0007g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0007g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0007g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0007g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0007g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0008g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0008g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0008g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0008g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0008g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0008g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0008g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0009g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0009g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0009g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0009g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0009g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0009g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0009g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0010g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0010g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0010g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0010g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0010g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0010g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0010g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0011g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0011g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0011g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0011g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0012g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0012g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0012g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0012g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0013g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0013g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0014g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0014g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0015g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0015g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0016g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0016g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0017g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0017g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0018g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0018g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0019g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0020g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0021g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0022g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0023g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0024g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0025g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0026g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0027g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0028g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0029g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0030g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0032g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0033g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0034g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0035g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0036g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0037g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0038g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0039g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0040g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0041g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0042g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0043g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0044g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0045g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0001c0001t0046g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0002c0004t0007g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0003c0003t0031g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| a0004c0002t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0015 | g0063 | EUR | GBR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | GBR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | CHS | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | CHS | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00639 | hp1 | a0001 | c0001 | t0009 | g0099 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | CHS | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00738 | hp1 | a0001 | c0001 | t0005 | g0048 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00738 | hp2 | a0001 | c0001 | t0030 | g0104 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0288 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01081 | hp1 | a0001 | c0001 | t0009 | g0096 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0049 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0231 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0250 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01106 | hp2 | a0001 | c0001 | t0005 | g0051 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0042 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0291 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01168 | hp2 | a0001 | c0001 | t0005 | g0061 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01169 | hp1 | a0001 | c0001 | t0005 | g0197 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0261 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01175 | hp2 | a0001 | c0001 | t0009 | g0187 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01256 | hp1 | a0001 | c0001 | t0005 | g0290 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0052 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0280 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0289 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01261 | hp2 | a0001 | c0001 | t0007 | g0046 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01358 | hp2 | a0001 | c0001 | t0036 | g0282 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0157 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0154 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0064 | EUR | IBS | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0152 | EUR | IBS | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01891 | hp1 | a0001 | c0001 | t0019 | g0040 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0085 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0032 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01934 | hp1 | a0001 | c0001 | t0028 | g0037 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0275 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02004 | hp2 | a0001 | c0001 | t0032 | g0003 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02015 | hp1 | a0001 | c0001 | t0038 | g0189 | EAS | KHV | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02055 | hp1 | a0001 | c0001 | t0025 | g0318 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02055 | hp2 | a0001 | c0001 | t0021 | g0090 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | KHV | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02074 | hp1 | a0001 | c0001 | t0009 | g0097 | EAS | KHV | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | KHV | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02145 | hp1 | a0003 | c0003 | t0031 | g0108 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02165 | hp1 | a0001 | c0001 | t0010 | g0181 | EAS | CDX | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CDX | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02257 | hp2 | a0001 | c0001 | t0006 | g0087 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0041 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0110 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02451 | hp1 | a0001 | c0001 | t0007 | g0298 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0081 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | KHV | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0316 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0053 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0066 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0067 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02630 | hp1 | a0001 | c0001 | t0041 | g0305 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02630 | hp2 | a0001 | c0001 | t0008 | g0116 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0058 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02723 | hp1 | a0001 | c0001 | t0034 | g0310 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0011 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0287 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02809 | hp1 | a0004 | c0002 | t0001 | g0315 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0317 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02896 | hp1 | a0001 | c0001 | t0008 | g0060 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0283 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0214 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0118 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ESN | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02965 | hp1 | a0001 | c0001 | t0018 | g0134 | AFR | ESN | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02965 | hp2 | a0001 | c0001 | t0043 | g0112 | AFR | ESN | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02970 | hp1 | a0001 | c0001 | t0046 | g0312 | AFR | ESN | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0198 | AFR | ESN | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | ESN | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02976 | hp2 | a0001 | c0001 | t0009 | g0089 | AFR | ESN | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0251 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0082 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03041 | hp2 | a0001 | c0001 | t0010 | g0313 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0080 | AFR | ESN | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03130 | hp2 | a0001 | c0001 | t0016 | g0107 | AFR | ESN | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03139 | hp1 | a0001 | c0001 | t0044 | g0320 | AFR | ESN | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0284 | AFR | ESN | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03195 | hp1 | a0001 | c0001 | t0010 | g0190 | AFR | ESN | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03195 | hp2 | a0001 | c0001 | t0016 | g0068 | AFR | ESN | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0111 | AFR | MSL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | MSL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0321 | AFR | MSL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0319 | AFR | MSL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0084 | AFR | MSL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03486 | hp1 | a0001 | c0001 | t0008 | g0004 | AFR | MSL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03486 | hp2 | a0001 | c0001 | t0010 | g0043 | AFR | MSL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03491 | hp2 | a0001 | c0001 | t0013 | g0093 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03492 | hp1 | a0001 | c0001 | t0013 | g0092 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | MSL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0222 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03688 | hp1 | a0001 | c0001 | t0014 | g0281 | SAS | STU | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0120 | SAS | STU | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0243 | SAS | PJL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0245 | SAS | BEB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0272 | SAS | BEB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03834 | hp2 | a0001 | c0001 | t0015 | g0016 | SAS | BEB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03942 | hp2 | a0001 | c0001 | t0014 | g0050 | SAS | BEB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | STU | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0246 | SAS | STU | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | BEB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0078 | SAS | STU | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0213 | SAS | STU | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG04204 | hp1 | a0001 | c0001 | t0045 | g0039 | SAS | STU | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0233 | SAS | STU | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18906 | hp1 | a0001 | c0001 | t0029 | g0074 | AFR | YRI | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | YRI | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18941 | hp1 | a0001 | c0001 | t0012 | g0017 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18948 | hp1 | a0001 | c0001 | t0011 | g0278 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18950 | hp1 | a0001 | c0001 | t0010 | g0184 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18950 | hp2 | a0001 | c0001 | t0010 | g0027 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18951 | hp1 | a0001 | c0001 | t0011 | g0193 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18972 | hp1 | a0001 | c0001 | t0037 | g0294 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18974 | hp1 | a0001 | c0001 | t0017 | g0151 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18985 | hp1 | a0001 | c0001 | t0010 | g0123 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18986 | hp1 | a0001 | c0001 | t0017 | g0173 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18988 | hp1 | a0001 | c0001 | t0023 | g0140 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA18992 | hp2 | a0001 | c0001 | t0035 | g0150 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19030 | hp1 | a0002 | c0004 | t0007 | g0047 | AFR | LWK | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19030 | hp2 | a0001 | c0001 | t0040 | g0194 | AFR | LWK | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19043 | hp1 | a0001 | c0001 | t0042 | g0109 | AFR | LWK | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0083 | AFR | LWK | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19075 | hp1 | a0001 | c0001 | t0012 | g0029 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19078 | hp1 | a0001 | c0001 | t0027 | g0182 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19081 | hp1 | a0001 | c0001 | t0012 | g0012 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19085 | hp1 | a0001 | c0001 | t0039 | g0105 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19087 | hp1 | a0001 | c0001 | t0011 | g0303 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19091 | hp1 | a0001 | c0001 | t0011 | g0257 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19091 | hp2 | a0001 | c0001 | t0012 | g0023 | EAS | JPT | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19240 | hp1 | a0001 | c0001 | t0024 | g0215 | AFR | YRI | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA19240 | hp2 | a0001 | c0001 | t0008 | g0004 | AFR | YRI | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ASW | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0285 | AFR | ASW | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA20752 | hp1 | a0001 | c0001 | t0022 | g0095 | EUR | TSI | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0115 | EUR | TSI | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0008 | EUR | TSI | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0269 | EUR | TSI | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA20905 | hp1 | a0001 | c0001 | t0007 | g0279 | SAS | GIH | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| NA20905 | hp2 | a0001 | c0001 | t0009 | g0098 | SAS | GIH | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0038 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG01123 | hp2 | a0001 | c0001 | t0009 | g0094 | AMR | CLM | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0086 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02486 | hp1 | a0001 | c0001 | t0033 | g0178 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02486 | hp2 | a0001 | c0001 | t0026 | g0322 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0296 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | ACB | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03471 | hp1 | a0001 | c0001 | t0008 | g0014 | AFR | MSL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG03471 | hp2 | a0001 | c0001 | t0018 | g0119 | AFR | MSL | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0103 | AFR | USA | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| HG06807 | hp2 | a0001 | c0001 | t0020 | g0091 | AFR | USA | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0136 | REF | REF | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0306 | REF | REF | RAB27B_chr18_54823477_54900516 | RAB27B | chr18 | 54823477 | 54900516 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:54877590
|
C | T | 1 | a0002 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.5C>T | p.Thr2Ile | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/6 | 248/7003 | 5/657 | 2/218 | chr18 | 54877590 | ||
| chr18:54888097
|
G | T | 1 | a0003 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.446G>T | p.Arg149Leu | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 5/6 | 689/7003 | 446/657 | 149/218 | chr18 | 54888097 | ||
| chr18:54889335
|
A | C | 1 | a0004 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.579A>C | p.Gln193His | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 822/7003 | 579/657 | 193/218 | chr18 | 54889335 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:54828694
|
C | A | 6 | a0001c0001t0009a0001c0001t0013a0001c0001t0019others(3): Show | 13 | HG00639.hp1 HG01081.hp1 HG01123.hp2 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-26C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/6 | 48892 | chr18 | 54828694 | |||||
| chr18:54889677
|
G | A | 1 | a0001c0001t0023 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*264G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 264 | chr18 | 54889677 | |||||
| chr18:54889747
|
C | T | 1 | a0001c0001t0046 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*334C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 334 | chr18 | 54889747 | |||||
| chr18:54889974
|
G | T | 1 | a0001c0001t0045 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*561G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 561 | chr18 | 54889974 | |||||
| chr18:54890011
|
C | T | 42 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(39): Show | 315 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(312): Show |
3_prime_UTR_variant | MODIFIER | c.*598C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 598 | chr18 | 54890011 | |||||
| chr18:54890017
|
G | A | 42 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(39): Show | 315 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(312): Show |
3_prime_UTR_variant | MODIFIER | c.*604G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 604 | chr18 | 54890017 | |||||
| chr18:54890033
|
G | A | 1 | a0001c0001t0024 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*620G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 620 | chr18 | 54890033 | |||||
| chr18:54890085
|
T | C | 43 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(40): Show | 317 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(314): Show |
3_prime_UTR_variant | MODIFIER | c.*672T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 672 | chr18 | 54890085 | |||||
| chr18:54890118
|
T | A | 1 | a0001c0001t0019 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*705T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 705 | chr18 | 54890118 | |||||
| chr18:54890358
|
C | A | 1 | a0001c0001t0020 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*945C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 945 | chr18 | 54890358 | |||||
| chr18:54890366
|
G | A | 1 | a0001c0001t0027 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*953G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 953 | chr18 | 54890366 | |||||
| chr18:54890551
|
C | T | 2 | a0001c0001t0008a0001c0001t0044 | 9 | HG02622.hp1 HG02630.hp2 HG02896.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1138C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 1138 | chr18 | 54890551 | |||||
| chr18:54890606
|
T | A | 1 | a0001c0001t0028 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1193T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 1193 | chr18 | 54890606 | |||||
| chr18:54890618
|
A | C | 1 | a0001c0001t0028 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1205A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 1205 | chr18 | 54890618 | |||||
| chr18:54890718
|
T | C | 3 | a0001c0001t0008a0001c0001t0029a0001c0001t0044 | 10 | HG02622.hp1 HG02630.hp2 HG02896.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1305T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 1305 | chr18 | 54890718 | |||||
| chr18:54890760
|
TG | T | 43 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(40): Show | 317 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(314): Show |
3_prime_UTR_variant | MODIFIER | c.*1348delG | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 1348 | chr18 | 54890760 | |||||
| chr18:54890807
|
G | A | 1 | a0001c0001t0029 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1394G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 1394 | chr18 | 54890807 | |||||
| chr18:54890987
|
G | GT | 40 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(37): Show | 308 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(305): Show |
3_prime_UTR_variant | MODIFIER | c.*1583dupT | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 1584 | INFO_REALIGN_3_PRIME | chr18 | 54890987 | ||||
| chr18:54891012
|
T | G | 3 | a0001c0001t0003a0001c0001t0015a0001c0001t0032 | 19 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1599T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 1599 | chr18 | 54891012 | |||||
| chr18:54891198
|
A | T | 1 | a0003c0003t0031 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1785A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 1785 | chr18 | 54891198 | |||||
| chr18:54891266
|
TAATAATT others(152): Show |
T | 1 | a0001c0001t0018 | 2 | HG02965.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1857_*2015del | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 1857 | INFO_REALIGN_3_PRIME | chr18 | 54891266 | ||||
| chr18:54891375
|
G | T | 1 | a0001c0001t0020 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1962G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 1962 | chr18 | 54891375 | |||||
| chr18:54891435
|
G | A | 42 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(39): Show | 315 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(312): Show |
3_prime_UTR_variant | MODIFIER | c.*2022G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 2022 | chr18 | 54891435 | |||||
| chr18:54891532
|
T | G | 1 | a0001c0001t0033 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2119T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 2119 | chr18 | 54891532 | |||||
| chr18:54891761
|
A | T | 1 | a0001c0001t0030 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2348A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 2348 | chr18 | 54891761 | |||||
| chr18:54892035
|
C | T | 4 | a0001c0001t0018a0001c0001t0042a0001c0001t0043others(1): Show | 5 | HG02145.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2622C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 2622 | chr18 | 54892035 | |||||
| chr18:54892063
|
G | A | 5 | a0001c0001t0005a0001c0001t0007a0001c0001t0013others(2): Show | 22 | HG00738.hp1 HG01081.hp2 HG01106.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2650G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 2650 | chr18 | 54892063 | |||||
| chr18:54892151
|
T | C | 1 | a0001c0001t0042 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2738T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 2738 | chr18 | 54892151 | |||||
| chr18:54892174
|
C | T | 1 | a0001c0001t0012 | 4 | NA18941.hp1 NA19075.hp1 NA19081.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2761C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 2761 | chr18 | 54892174 | |||||
| chr18:54892221
|
A | G | 1 | a0001c0001t0041 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2808A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 2808 | chr18 | 54892221 | |||||
| chr18:54892229
|
C | A | 1 | a0001c0001t0005 | 11 | HG00738.hp1 HG01081.hp2 HG01106.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2816C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 2816 | chr18 | 54892229 | |||||
| chr18:54892338
|
G | A | 1 | a0001c0001t0034 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2925G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 2925 | chr18 | 54892338 | |||||
| chr18:54892404
|
G | A | 1 | a0001c0001t0021 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2991G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 2991 | chr18 | 54892404 | |||||
| chr18:54892474
|
T | A | 13 | a0001c0001t0002a0001c0001t0006a0001c0001t0015others(10): Show | 88 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*3061T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 3061 | chr18 | 54892474 | |||||
| chr18:54892702
|
C | A | 1 | a0001c0001t0035 | 1 | NA18992.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3289C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 3289 | chr18 | 54892702 | |||||
| chr18:54892743
|
C | T | 1 | a0001c0001t0032 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3330C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 3330 | chr18 | 54892743 | |||||
| chr18:54892747
|
C | T | 1 | a0001c0001t0041 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3334C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 3334 | chr18 | 54892747 | |||||
| chr18:54892877
|
C | T | 1 | a0001c0001t0011 | 4 | NA18948.hp1 NA18951.hp1 NA19087.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3464C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 3464 | chr18 | 54892877 | |||||
| chr18:54893262
|
G | T | 43 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(40): Show | 317 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(314): Show |
3_prime_UTR_variant | MODIFIER | c.*3849G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 3849 | chr18 | 54893262 | |||||
| chr18:54893473
|
T | C | 1 | a0001c0001t0025 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4060T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 4060 | chr18 | 54893473 | |||||
| chr18:54893519
|
A | G | 1 | a0001c0001t0040 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4106A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 4106 | chr18 | 54893519 | |||||
| chr18:54893555
|
G | T | 1 | a0001c0001t0026 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4142G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 4142 | chr18 | 54893555 | |||||
| chr18:54893653
|
C | T | 2 | a0001c0001t0042a0001c0001t0043 | 2 | HG02965.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4240C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 4240 | chr18 | 54893653 | |||||
| chr18:54893778
|
C | A | 43 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(40): Show | 317 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(314): Show |
3_prime_UTR_variant | MODIFIER | c.*4365C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 4365 | chr18 | 54893778 | |||||
| chr18:54893899
|
A | G | 1 | a0001c0001t0020 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4486A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 4486 | chr18 | 54893899 | |||||
| chr18:54893992
|
C | T | 1 | a0001c0001t0006 | 9 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4579C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 4579 | chr18 | 54893992 | |||||
| chr18:54894025
|
A | G | 1 | a0001c0001t0036 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4612A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 4612 | chr18 | 54894025 | |||||
| chr18:54894085
|
T | G | 1 | a0001c0001t0017 | 2 | NA18974.hp1 NA18986.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4672T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 4672 | chr18 | 54894085 | |||||
| chr18:54894112
|
G | A | 1 | a0001c0001t0006 | 9 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4699G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 4699 | chr18 | 54894112 | |||||
| chr18:54894192
|
G | T | 1 | a0001c0001t0016 | 2 | HG03130.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4779G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 4779 | chr18 | 54894192 | |||||
| chr18:54894215
|
A | G | 43 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(40): Show | 317 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(314): Show |
3_prime_UTR_variant | MODIFIER | c.*4802A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 4802 | chr18 | 54894215 | |||||
| chr18:54894281
|
A | G | 1 | a0001c0001t0020 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4868A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 4868 | chr18 | 54894281 | |||||
| chr18:54894615
|
G | T | 1 | a0001c0001t0044 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5202G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 5202 | chr18 | 54894615 | |||||
| chr18:54895120
|
TTTAG | T | 43 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(40): Show | 317 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(314): Show |
3_prime_UTR_variant | MODIFIER | c.*5713_*5716delTAGT | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 5713 | INFO_REALIGN_3_PRIME | chr18 | 54895120 | ||||
| chr18:54895231
|
G | A | 1 | a0001c0001t0037 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5818G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 5818 | chr18 | 54895231 | |||||
| chr18:54895257
|
A | G | 1 | a0001c0001t0039 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5844A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 5844 | chr18 | 54895257 | |||||
| chr18:54895335
|
A | G | 1 | a0001c0001t0038 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5922A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 6/6 | 5922 | chr18 | 54895335 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:54828772
|
C | T | 1 | a0001c0001t0001g0324 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-20+72C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54828772 | ||||||
| chr18:54828792
|
CTG | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(185): Show | 194 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.-20+107_-20+108del others(2): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54828792 | |||||
| chr18:54828811
|
T | A | 1 | a0001c0001t0002g0191 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-20+111T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54828811 | ||||||
| chr18:54828821
|
C | A | 1 | a0001c0001t0002g0192 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-20+121C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54828821 | ||||||
| chr18:54828944
|
A | G | 1 | a0001c0001t0010g0190 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-20+244A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54828944 | ||||||
| chr18:54829059
|
T | C | 33 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(30): Show | 34 | HG00438.hp1 HG00558.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-20+359T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54829059 | ||||||
| chr18:54829105
|
T | C | 1 | a0001c0001t0011g0193 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-20+405T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54829105 | ||||||
| chr18:54829179
|
T | G | 1 | a0001c0001t0001g0010 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-20+479T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54829179 | ||||||
| chr18:54829254
|
T | C | 1 | a0001c0001t0019g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-20+554T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54829254 | ||||||
| chr18:54829690
|
A | G | 11 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0002g0033others(8): Show | 11 | HG01074.hp1 HG01123.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.-20+990A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54829690 | ||||||
| chr18:54829973
|
A | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(87): Show | 95 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.-20+1273A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54829973 | ||||||
| chr18:54830305
|
C | T | 1 | a0001c0001t0045g0039 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-20+1605C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54830305 | ||||||
| chr18:54830328
|
T | C | 2 | a0001c0001t0006g0041a0001c0001t0006g0042 | 2 | HG01109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-20+1628T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54830328 | ||||||
| chr18:54830379
|
C | T | 1 | a0001c0001t0038g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-20+1679C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54830379 | ||||||
| chr18:54830502
|
G | A | 11 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0002g0033others(8): Show | 11 | HG01074.hp1 HG01123.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.-20+1802G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54830502 | ||||||
| chr18:54830610
|
AT | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0031a0001c0001t0001g0036others(9): Show | 12 | HG01074.hp1 HG01123.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.-20+1920delT | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54830610 | |||||
| chr18:54830762
|
C | T | 1 | a0001c0001t0001g0323 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-20+2062C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54830762 | ||||||
| chr18:54830946
|
T | A | 1 | a0001c0001t0040g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-20+2246T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54830946 | ||||||
| chr18:54830986
|
T | C | 1 | a0001c0001t0039g0105 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-20+2286T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54830986 | ||||||
| chr18:54831059
|
C | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(87): Show | 95 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.-20+2359C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54831059 | ||||||
| chr18:54831069
|
C | A | 47 | a0001c0001t0001g0045a0001c0001t0001g0054a0001c0001t0001g0055others(44): Show | 47 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.-20+2369C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54831069 | ||||||
| chr18:54831129
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-20+2429A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54831129 | ||||||
| chr18:54831318
|
C | T | 21 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(18): Show | 22 | HG00438.hp1 HG00558.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.-20+2618C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54831318 | ||||||
| chr18:54831389
|
AATGGGGA others(9): Show |
A | 1 | a0001c0001t0001g0188 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-20+2690_-20+2705d others(18): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54831389 | ||||||
| chr18:54831499
|
C | T | 1 | a0001c0001t0019g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-20+2799C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54831499 | ||||||
| chr18:54831545
|
C | T | 21 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(18): Show | 22 | HG00438.hp1 HG00558.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.-20+2845C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54831545 | ||||||
| chr18:54831546
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-20+2846G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54831546 | ||||||
| chr18:54831570
|
G | C | 88 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(85): Show | 93 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.-20+2870G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54831570 | ||||||
| chr18:54831781
|
CT | C | 15 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(12): Show | 15 | HG00639.hp1 HG01081.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.-20+3090delT | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54831781 | |||||
| chr18:54831838
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-20+3138C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54831838 | ||||||
| chr18:54831868
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-20+3168C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54831868 | ||||||
| chr18:54831929
|
C | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(86): Show | 94 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.-20+3229C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54831929 | ||||||
| chr18:54831982
|
G | T | 7 | a0001c0001t0006g0081a0001c0001t0006g0083a0001c0001t0006g0085others(4): Show | 7 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20+3282G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54831982 | ||||||
| chr18:54832053
|
T | C | 305 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(302): Show | 313 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(310): Show |
intron_variant | MODIFIER | c.-20+3353T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54832053 | ||||||
| chr18:54832054
|
G | A | 11 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0002g0033others(8): Show | 11 | HG01074.hp1 HG01123.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.-20+3354G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54832054 | ||||||
| chr18:54832121
|
T | A | 1 | a0001c0001t0001g0106 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-20+3421T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54832121 | ||||||
| chr18:54832217
|
C | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(86): Show | 94 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.-20+3517C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54832217 | ||||||
| chr18:54832395
|
T | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(86): Show | 94 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.-20+3695T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54832395 | ||||||
| chr18:54832470
|
T | C | 1 | a0001c0001t0002g0195 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-20+3770T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54832470 | ||||||
| chr18:54832570
|
T | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(86): Show | 94 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.-20+3870T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54832570 | ||||||
| chr18:54832780
|
G | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(71): Show | 78 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.-20+4080G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54832780 | ||||||
| chr18:54832829
|
C | T | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02647.hp1 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-20+4129C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54832829 | ||||||
| chr18:54832854
|
G | A | 12 | a0001c0001t0009g0089a0001c0001t0009g0094a0001c0001t0009g0096others(9): Show | 12 | HG00639.hp1 HG01081.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.-20+4154G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54832854 | ||||||
| chr18:54832892
|
A | G | 15 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(12): Show | 15 | HG00639.hp1 HG01081.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.-20+4192A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54832892 | ||||||
| chr18:54833000
|
A | C | 1 | a0001c0001t0001g0088 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-20+4300A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833000 | ||||||
| chr18:54833020
|
G | A | 1 | a0001c0001t0010g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-20+4320G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833020 | ||||||
| chr18:54833061
|
C | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(86): Show | 94 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.-20+4361C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833061 | ||||||
| chr18:54833118
|
G | A | 1 | a0001c0001t0002g0196 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-20+4418G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833118 | ||||||
| chr18:54833234
|
C | CTTTT | 130 | a0001c0001t0001g0045a0001c0001t0001g0188a0001c0001t0001g0200others(127): Show | 132 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(129): Show |
intron_variant | MODIFIER | c.-20+4545_-20+4548d others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54833234 | |||||
| chr18:54833234
|
C | CTTTTT | 68 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(65): Show | 69 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.-20+4544_-20+4548d others(7): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54833234 | |||||
| chr18:54833234
|
C | CTTTTTT | 14 | a0001c0001t0001g0010a0001c0001t0001g0031a0001c0001t0001g0036others(11): Show | 14 | HG01074.hp1 HG01123.hp1 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.-20+4543_-20+4548d others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54833234 | |||||
| chr18:54833234
|
C | T | 1 | a0001c0001t0004g0080 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-20+4534C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833234 | ||||||
| chr18:54833272
|
G | C | 1 | a0001c0001t0006g0041 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-20+4572G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833272 | ||||||
| chr18:54833274
|
T | G | 1 | a0001c0001t0041g0305 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-20+4574T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833274 | ||||||
| chr18:54833289
|
C | T | 2 | a0001c0001t0001g0299a0001c0001t0007g0298 | 2 | HG00735.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-20+4589C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833289 | ||||||
| chr18:54833370
|
G | A | 1 | a0001c0001t0016g0107 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-20+4670G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833370 | ||||||
| chr18:54833528
|
T | G | 12 | a0001c0001t0001g0010a0001c0001t0001g0031a0001c0001t0001g0036others(9): Show | 12 | HG01074.hp1 HG01123.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.-20+4828T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833528 | ||||||
| chr18:54833588
|
A | G | 3 | a0001c0001t0001g0045a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | HG02602.hp2 HG03704.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-20+4888A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833588 | ||||||
| chr18:54833662
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-20+4962C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833662 | ||||||
| chr18:54833781
|
A | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(86): Show | 94 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.-20+5081A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833781 | ||||||
| chr18:54833784
|
G | C | 1 | a0001c0001t0003g0120 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-20+5084G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833784 | ||||||
| chr18:54833785
|
G | T | 1 | a0001c0001t0003g0120 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-20+5085G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833785 | ||||||
| chr18:54833823
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-20+5123G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833823 | ||||||
| chr18:54833869
|
CAG | C | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02647.hp1 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-20+5176_-20+5177d others(4): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54833869 | |||||
| chr18:54833939
|
A | G | 21 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(18): Show | 22 | HG00438.hp1 HG00558.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.-20+5239A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833939 | ||||||
| chr18:54833989
|
T | C | 1 | a0001c0001t0004g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-20+5289T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54833989 | ||||||
| chr18:54834331
|
A | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(202): Show | 212 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(209): Show |
intron_variant | MODIFIER | c.-20+5631A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54834331 | ||||||
| chr18:54834573
|
A | T | 1 | a0001c0001t0002g0075 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-20+5873A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54834573 | ||||||
| chr18:54834575
|
C | T | 1 | a0001c0001t0002g0075 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-20+5875C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54834575 | ||||||
| chr18:54834673
|
G | GTA | 127 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(124): Show | 132 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.-20+5981_-20+5982d others(4): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54834673 | |||||
| chr18:54834681
|
A | ATATG | 125 | a0001c0001t0001g0010a0001c0001t0001g0113a0001c0001t0001g0117others(122): Show | 128 | HG00558.hp2 HG00621.hp1 HG00642.hp2 others(125): Show |
intron_variant | MODIFIER | c.-20+5982_-20+5983i others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54834681 | |||||
| chr18:54834681
|
A | ATATGTG | 4 | a0001c0001t0001g0295a0001c0001t0001g0297a0001c0001t0004g0198others(1): Show | 4 | HG02145.hp2 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+5982_-20+5983i others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54834681 | |||||
| chr18:54834681
|
A | ATG | 49 | a0001c0001t0001g0045a0001c0001t0001g0054a0001c0001t0001g0055others(46): Show | 49 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.-20+5998_-20+5999d others(4): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54834681 | |||||
| chr18:54834719
|
GAAGAGAT others(2199): Show |
G | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02647.hp1 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-20+6024_-20+8229d others(2): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54834719 | |||||
| chr18:54834753
|
G | A | 1 | a0001c0001t0001g0200 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-20+6053G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54834753 | ||||||
| chr18:54834808
|
T | C | 1 | a0001c0001t0007g0046 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-20+6108T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54834808 | ||||||
| chr18:54834949
|
A | G | 7 | a0001c0001t0004g0316a0001c0001t0004g0317a0001c0001t0004g0319others(4): Show | 7 | HG02055.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+6249A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54834949 | ||||||
| chr18:54834959
|
A | T | 5 | a0001c0001t0001g0180a0001c0001t0001g0183a0001c0001t0010g0181others(2): Show | 5 | HG00609.hp2 HG02165.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20+6259A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54834959 | ||||||
| chr18:54835068
|
A | G | 1 | a0001c0001t0037g0294 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-20+6368A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835068 | ||||||
| chr18:54835073
|
C | T | 1 | a0001c0001t0001g0323 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-20+6373C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835073 | ||||||
| chr18:54835077
|
T | C | 2 | a0001c0001t0001g0015a0001c0001t0001g0030 | 2 | NA18947.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.-20+6377T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835077 | ||||||
| chr18:54835333
|
C | T | 1 | a0001c0001t0018g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-20+6633C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835333 | ||||||
| chr18:54835528
|
A | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(203): Show | 213 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(210): Show |
intron_variant | MODIFIER | c.-20+6828A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835528 | ||||||
| chr18:54835565
|
C | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(202): Show | 212 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(209): Show |
intron_variant | MODIFIER | c.-20+6865C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835565 | ||||||
| chr18:54835566
|
G | A | 11 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0002g0033others(8): Show | 11 | HG01074.hp1 HG01123.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.-20+6866G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835566 | ||||||
| chr18:54835613
|
C | T | 3 | a0001c0001t0004g0013a0001c0001t0006g0011a0001c0001t0008g0014 | 3 | HG02723.hp2 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-20+6913C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835613 | ||||||
| chr18:54835629
|
A | C | 1 | a0001c0001t0001g0179 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-20+6929A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835629 | ||||||
| chr18:54835652
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0002g0114 | 2 | HG02818.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-20+6952G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835652 | ||||||
| chr18:54835656
|
T | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(203): Show | 213 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(210): Show |
intron_variant | MODIFIER | c.-20+6956T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835656 | ||||||
| chr18:54835716
|
C | T | 2 | a0001c0001t0001g0292a0001c0001t0001g0293 | 2 | NA19062.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.-20+7016C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835716 | ||||||
| chr18:54835717
|
C | T | 1 | a0001c0001t0033g0178 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-20+7017C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835717 | ||||||
| chr18:54835747
|
T | C | 1 | a0002c0004t0007g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-20+7047T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835747 | ||||||
| chr18:54835821
|
C | T | 6 | a0001c0001t0001g0299a0001c0001t0002g0288a0001c0001t0005g0197others(3): Show | 6 | HG00735.hp2 HG00741.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+7121C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835821 | ||||||
| chr18:54835869
|
T | G | 79 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(76): Show | 80 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.-20+7169T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835869 | ||||||
| chr18:54835908
|
C | T | 1 | a0001c0001t0039g0105 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-20+7208C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835908 | ||||||
| chr18:54835969
|
T | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0122others(9): Show | 15 | HG00609.hp1 HG01169.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+7269T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835969 | ||||||
| chr18:54835975
|
C | A | 3 | a0001c0001t0004g0013a0001c0001t0006g0011a0001c0001t0008g0014 | 3 | HG02723.hp2 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-20+7275C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835975 | ||||||
| chr18:54835979
|
A | C | 1 | a0004c0002t0001g0315 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-20+7279A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54835979 | ||||||
| chr18:54836082
|
A | C | 95 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(92): Show | 96 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.-20+7382A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54836082 | ||||||
| chr18:54836234
|
A | G | 1 | a0001c0001t0003g0038 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-20+7534A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54836234 | ||||||
| chr18:54836358
|
G | A | 206 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(203): Show | 213 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(210): Show |
intron_variant | MODIFIER | c.-20+7658G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54836358 | ||||||
| chr18:54836392
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-20+7692C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54836392 | ||||||
| chr18:54836423
|
T | G | 95 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(92): Show | 96 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.-20+7723T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54836423 | ||||||
| chr18:54836796
|
A | G | 301 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(298): Show | 309 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(306): Show |
intron_variant | MODIFIER | c.-20+8096A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54836796 | ||||||
| chr18:54836811
|
G | T | 1 | a0001c0001t0012g0029 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-20+8111G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54836811 | ||||||
| chr18:54837007
|
A | G | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG02683.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-20+8307A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54837007 | ||||||
| chr18:54837021
|
CCTA | C | 118 | a0001c0001t0001g0188a0001c0001t0001g0200a0001c0001t0001g0201others(115): Show | 120 | HG00558.hp2 HG00621.hp1 HG00642.hp2 others(117): Show |
intron_variant | MODIFIER | c.-20+8325_-20+8327d others(5): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54837021 | |||||
| chr18:54837087
|
T | C | 1 | a0001c0001t0002g0191 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-20+8387T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54837087 | ||||||
| chr18:54837112
|
TAGAG | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(202): Show | 212 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(209): Show |
intron_variant | MODIFIER | c.-20+8415_-20+8418d others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54837112 | |||||
| chr18:54837124
|
T | C | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02647.hp1 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-20+8424T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54837124 | ||||||
| chr18:54837267
|
A | G | 67 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(64): Show | 68 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.-20+8567A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54837267 | ||||||
| chr18:54837482
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-20+8782G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54837482 | ||||||
| chr18:54837538
|
C | A | 3 | a0001c0001t0004g0013a0001c0001t0006g0011a0001c0001t0008g0014 | 3 | HG02723.hp2 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-20+8838C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54837538 | ||||||
| chr18:54837792
|
A | G | 1 | a0001c0001t0006g0087 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-20+9092A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54837792 | ||||||
| chr18:54837796
|
A | G | 11 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0002g0033others(8): Show | 11 | HG01074.hp1 HG01123.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.-20+9096A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54837796 | ||||||
| chr18:54837880
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-20+9180G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54837880 | ||||||
| chr18:54838095
|
A | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(211): Show | 221 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(218): Show |
intron_variant | MODIFIER | c.-20+9395A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54838095 | ||||||
| chr18:54838484
|
C | A | 2 | a0001c0001t0004g0103a0001c0001t0030g0104 | 2 | HG00738.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-20+9784C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54838484 | ||||||
| chr18:54838636
|
A | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(211): Show | 221 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(218): Show |
intron_variant | MODIFIER | c.-20+9936A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54838636 | ||||||
| chr18:54838651
|
A | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(211): Show | 221 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(218): Show |
intron_variant | MODIFIER | c.-20+9951A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54838651 | ||||||
| chr18:54838722
|
G | A | 2 | a0001c0001t0005g0115a0001c0001t0018g0119 | 2 | HG03471.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-20+10022G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54838722 | ||||||
| chr18:54838731
|
G | A | 83 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(80): Show | 84 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.-20+10031G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54838731 | ||||||
| chr18:54838846
|
A | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(211): Show | 221 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(218): Show |
intron_variant | MODIFIER | c.-20+10146A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54838846 | ||||||
| chr18:54838957
|
A | G | 4 | a0001c0001t0009g0089a0001c0001t0019g0040a0001c0001t0020g0091others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+10257A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54838957 | ||||||
| chr18:54838960
|
G | A | 1 | a0001c0001t0041g0305 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-20+10260G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54838960 | ||||||
| chr18:54839004
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-20+10304G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54839004 | ||||||
| chr18:54839181
|
G | A | 4 | a0001c0001t0004g0110a0001c0001t0004g0111a0001c0001t0042g0109others(1): Show | 4 | HG02145.hp1 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+10481G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54839181 | ||||||
| chr18:54839354
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-20+10654T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54839354 | ||||||
| chr18:54839355
|
A | C | 11 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0002g0033others(8): Show | 11 | HG01074.hp1 HG01123.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.-20+10655A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54839355 | ||||||
| chr18:54839698
|
C | T | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02647.hp1 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-20+10998C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54839698 | ||||||
| chr18:54839736
|
G | A | 304 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(301): Show | 312 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(309): Show |
intron_variant | MODIFIER | c.-20+11036G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54839736 | ||||||
| chr18:54839742
|
G | T | 305 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(302): Show | 313 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(310): Show |
intron_variant | MODIFIER | c.-20+11042G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54839742 | ||||||
| chr18:54839847
|
T | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(211): Show | 221 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(218): Show |
intron_variant | MODIFIER | c.-20+11147T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54839847 | ||||||
| chr18:54839859
|
T | C | 67 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(64): Show | 68 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.-20+11159T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54839859 | ||||||
| chr18:54839940
|
T | A | 1 | a0001c0001t0002g0202 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-20+11240T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54839940 | ||||||
| chr18:54840039
|
A | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(211): Show | 221 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(218): Show |
intron_variant | MODIFIER | c.-20+11339A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54840039 | ||||||
| chr18:54840133
|
G | A | 1 | a0001c0001t0008g0116 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-20+11433G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54840133 | ||||||
| chr18:54840138
|
G | A | 1 | a0001c0001t0002g0203 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-20+11438G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54840138 | ||||||
| chr18:54840228
|
C | G | 1 | a0001c0001t0002g0287 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-20+11528C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54840228 | ||||||
| chr18:54840619
|
A | AAAT | 305 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(302): Show | 313 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(310): Show |
intron_variant | MODIFIER | c.-20+11922_-20+1192 others(7): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54840619 | |||||
| chr18:54840646
|
T | A | 214 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(211): Show | 221 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(218): Show |
intron_variant | MODIFIER | c.-20+11946T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54840646 | ||||||
| chr18:54840874
|
G | C | 1 | a0001c0001t0006g0087 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-20+12174G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54840874 | ||||||
| chr18:54840944
|
C | T | 3 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0010g0027 | 3 | HG00438.hp1 NA18950.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.-20+12244C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54840944 | ||||||
| chr18:54840976
|
G | A | 2 | a0001c0001t0003g0002a0001c0001t0015g0016 | 3 | HG01070.hp2 HG01071.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-20+12276G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54840976 | ||||||
| chr18:54841151
|
T | TGGCG | 13 | a0001c0001t0001g0030a0001c0001t0001g0062a0001c0001t0001g0065others(10): Show | 13 | HG00099.hp1 HG01168.hp2 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.-20+12454_-20+1245 others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54841151 | |||||
| chr18:54841154
|
C | CG | 23 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0171others(20): Show | 24 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.-20+12458dupG | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54841154 | |||||
| chr18:54841154
|
C | CGG | 115 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0113others(112): Show | 120 | HG00099.hp2 HG00558.hp2 HG00609.hp2 others(117): Show |
intron_variant | MODIFIER | c.-20+12457_-20+1245 others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54841154 | |||||
| chr18:54841154
|
C | CGGG | 39 | a0001c0001t0001g0005a0001c0001t0001g0122a0001c0001t0001g0136others(36): Show | 40 | HG00609.hp1 HG00621.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-20+12456_-20+1245 others(7): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54841154 | |||||
| chr18:54841154
|
C | CGGGCG | 28 | a0001c0001t0001g0024a0001c0001t0001g0036a0001c0001t0001g0054others(25): Show | 28 | HG01081.hp2 HG01106.hp2 HG01256.hp2 others(25): Show |
intron_variant | MODIFIER | c.-20+12457_-20+1245 others(9): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54841154 | |||||
| chr18:54841154
|
C | CGGGCGG | 19 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(16): Show | 19 | HG00438.hp1 HG00558.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.-20+12457_-20+1245 others(10): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54841154 | |||||
| chr18:54841154
|
C | CGGGCGGG | 7 | a0001c0001t0001g0018a0001c0001t0001g0031a0001c0001t0001g0045others(4): Show | 7 | HG01123.hp1 HG01928.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+12457_-20+1245 others(11): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54841154 | |||||
| chr18:54841154
|
C | CGGGG | 15 | a0001c0001t0001g0025a0001c0001t0001g0200a0001c0001t0001g0207others(12): Show | 15 | HG02109.hp2 HG02922.hp2 HG02965.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+12455_-20+1245 others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54841154 | |||||
| chr18:54841155
|
G | GGGC | 12 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071others(9): Show | 12 | HG00639.hp2 HG00735.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20+12457_-20+1245 others(7): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54841155 | |||||
| chr18:54841159
|
C | G | 300 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(297): Show | 308 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(305): Show |
intron_variant | MODIFIER | c.-20+12459C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54841159 | ||||||
| chr18:54841159
|
C | T | 1 | a0001c0001t0012g0012 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-20+12459C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54841159 | ||||||
| chr18:54841160
|
G | GC | 4 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0001t0002g0300others(1): Show | 4 | NA18965.hp1 NA18969.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+12460_-20+1246 others(5): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54841160 | ||||||
| chr18:54841162
|
T | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 310 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(307): Show |
intron_variant | MODIFIER | c.-20+12462T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54841162 | ||||||
| chr18:54841183
|
C | T | 1 | a0001c0001t0003g0038 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-20+12483C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54841183 | ||||||
| chr18:54841250
|
A | C | 304 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(301): Show | 312 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(309): Show |
intron_variant | MODIFIER | c.-20+12550A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54841250 | ||||||
| chr18:54841405
|
A | G | 2 | a0001c0001t0003g0002a0001c0001t0015g0016 | 3 | HG01070.hp2 HG01071.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-20+12705A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54841405 | ||||||
| chr18:54841566
|
G | A | 1 | a0001c0001t0043g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-20+12866G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54841566 | ||||||
| chr18:54841732
|
A | C | 304 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(301): Show | 312 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(309): Show |
intron_variant | MODIFIER | c.-20+13032A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54841732 | ||||||
| chr18:54841778
|
T | A | 13 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0001g0141others(10): Show | 13 | HG01074.hp1 HG01123.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-20+13078T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54841778 | ||||||
| chr18:54841943
|
C | G | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | HG01975.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.-20+13243C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54841943 | ||||||
| chr18:54842079
|
C | T | 1 | a0001c0001t0004g0067 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-20+13379C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54842079 | ||||||
| chr18:54842313
|
T | TAGAG | 304 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(301): Show | 312 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(309): Show |
intron_variant | MODIFIER | c.-20+13616_-20+1361 others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54842313 | |||||
| chr18:54842399
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-20+13699C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54842399 | ||||||
| chr18:54842411
|
A | G | 1 | a0001c0001t0004g0111 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-20+13711A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54842411 | ||||||
| chr18:54842521
|
C | CA | 304 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(301): Show | 312 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(309): Show |
intron_variant | MODIFIER | c.-20+13823dupA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54842521 | |||||
| chr18:54842602
|
C | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(67): Show | 74 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.-20+13902C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54842602 | ||||||
| chr18:54842603
|
G | A | 1 | a0001c0001t0003g0231 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-20+13903G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54842603 | ||||||
| chr18:54842651
|
C | T | 91 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(88): Show | 92 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.-20+13951C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54842651 | ||||||
| chr18:54842768
|
G | A | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02647.hp1 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-20+14068G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54842768 | ||||||
| chr18:54842778
|
C | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG00438.hp1 HG03831.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20+14078C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54842778 | ||||||
| chr18:54842863
|
C | G | 1 | a0001c0001t0001g0030 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-20+14163C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54842863 | ||||||
| chr18:54842974
|
T | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(210): Show | 220 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(217): Show |
intron_variant | MODIFIER | c.-20+14274T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54842974 | ||||||
| chr18:54842981
|
A | G | 1 | a0001c0001t0002g0272 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-20+14281A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54842981 | ||||||
| chr18:54843146
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-20+14446T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54843146 | ||||||
| chr18:54843148
|
A | G | 2 | a0001c0001t0004g0103a0001c0001t0030g0104 | 2 | HG00738.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-20+14448A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54843148 | ||||||
| chr18:54843200
|
G | C | 4 | a0001c0001t0004g0110a0001c0001t0004g0111a0001c0001t0042g0109others(1): Show | 4 | HG02145.hp1 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+14500G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54843200 | ||||||
| chr18:54843357
|
ACT | A | 3 | a0001c0001t0004g0013a0001c0001t0006g0011a0001c0001t0008g0014 | 3 | HG02723.hp2 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-20+14660_-20+1466 others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54843357 | |||||
| chr18:54843360
|
CT | C | 205 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(202): Show | 208 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(205): Show |
intron_variant | MODIFIER | c.-20+14671delT | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54843360 | |||||
| chr18:54843360
|
CTT | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(84): Show | 92 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.-20+14670_-20+1467 others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54843360 | |||||
| chr18:54843758
|
C | A | 2 | a0001c0001t0009g0089a0001c0001t0021g0090 | 2 | HG02055.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-20+15058C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54843758 | ||||||
| chr18:54843834
|
C | G | 1 | a0001c0001t0029g0074 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-20+15134C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54843834 | ||||||
| chr18:54843871
|
T | G | 1 | a0001c0001t0001g0207 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-20+15171T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54843871 | ||||||
| chr18:54844003
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-20+15303T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54844003 | ||||||
| chr18:54844090
|
A | C | 91 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(88): Show | 92 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.-20+15390A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54844090 | ||||||
| chr18:54844143
|
T | G | 14 | a0001c0001t0001g0010a0001c0001t0001g0031a0001c0001t0001g0036others(11): Show | 14 | HG01074.hp1 HG01123.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-20+15443T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54844143 | ||||||
| chr18:54844345
|
C | T | 1 | a0001c0001t0029g0074 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-20+15645C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54844345 | ||||||
| chr18:54844375
|
C | CTTCT | 3 | a0001c0001t0001g0323a0001c0001t0004g0316a0001c0001t0004g0317 | 3 | HG00642.hp1 HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-20+15698_-20+1570 others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54844375 | |||||
| chr18:54844375
|
CTTCT | C | 3 | a0001c0001t0001g0270a0001c0001t0002g0271a0001c0001t0009g0098 | 3 | HG00621.hp1 HG04184.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-20+15698_-20+1570 others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54844375 | |||||
| chr18:54844375
|
CTTCTTTC others(1): Show |
C | 23 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0020others(20): Show | 24 | HG00438.hp1 HG00558.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.-20+15694_-20+1570 others(12): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54844375 | |||||
| chr18:54844408
|
C | CTTT | 49 | a0001c0001t0001g0036a0001c0001t0001g0054a0001c0001t0001g0055others(46): Show | 49 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.-20+15724_-20+1572 others(7): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54844408 | |||||
| chr18:54844408
|
CTT | C | 13 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0230others(10): Show | 13 | HG01069.hp2 HG01071.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.-20+15725_-20+1572 others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54844408 | |||||
| chr18:54844408
|
CTTT | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(195): Show | 205 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(202): Show |
intron_variant | MODIFIER | c.-20+15724_-20+1572 others(7): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54844408 | |||||
| chr18:54844412
|
T | TC | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02647.hp1 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-20+15712_-20+1571 others(5): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54844412 | ||||||
| chr18:54844418
|
T | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG00673.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.-20+15718T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54844418 | ||||||
| chr18:54844481
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-20+15781T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54844481 | ||||||
| chr18:54844581
|
A | G | 1 | a0001c0001t0004g0110 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-20+15881A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54844581 | ||||||
| chr18:54844794
|
C | T | 1 | a0001c0001t0002g0213 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-20+16094C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54844794 | ||||||
| chr18:54844804
|
C | T | 1 | a0001c0001t0003g0269 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-20+16104C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54844804 | ||||||
| chr18:54845088
|
A | G | 1 | a0001c0001t0002g0166 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-20+16388A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54845088 | ||||||
| chr18:54845212
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-20+16512G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54845212 | ||||||
| chr18:54845213
|
C | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(210): Show | 220 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(217): Show |
intron_variant | MODIFIER | c.-20+16513C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54845213 | ||||||
| chr18:54845372
|
A | C | 25 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(22): Show | 26 | HG00438.hp1 HG00558.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.-20+16672A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54845372 | ||||||
| chr18:54845405
|
C | CAAAA | 212 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 219 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(216): Show |
intron_variant | MODIFIER | c.-20+16716_-20+1671 others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54845405 | |||||
| chr18:54845405
|
C | CAAAAA | 87 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(84): Show | 88 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.-20+16715_-20+1671 others(9): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54845405 | |||||
| chr18:54845415
|
A | T | 18 | a0001c0001t0001g0009a0001c0001t0001g0307a0001c0001t0001g0308others(15): Show | 19 | HG00642.hp1 HG01243.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-20+16715A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54845415 | ||||||
| chr18:54845420
|
T | A | 1 | a0001c0001t0001g0088 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-20+16720T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54845420 | ||||||
| chr18:54845421
|
A | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 310 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(307): Show |
intron_variant | MODIFIER | c.-20+16721A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54845421 | ||||||
| chr18:54845426
|
A | G | 1 | a0001c0001t0002g0165 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-20+16726A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54845426 | ||||||
| chr18:54845545
|
G | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(210): Show | 220 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(217): Show |
intron_variant | MODIFIER | c.-20+16845G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54845545 | ||||||
| chr18:54845549
|
C | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0128others(1): Show | 7 | HG01169.hp2 HG01943.hp1 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+16849C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54845549 | ||||||
| chr18:54845616
|
G | A | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02647.hp1 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-20+16916G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54845616 | ||||||
| chr18:54845836
|
A | G | 2 | a0001c0001t0004g0321a0001c0001t0026g0322 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-20+17136A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54845836 | ||||||
| chr18:54845888
|
C | A | 1 | a0001c0001t0029g0074 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-20+17188C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54845888 | ||||||
| chr18:54845992
|
A | G | 4 | a0001c0001t0008g0060a0001c0001t0008g0066a0001c0001t0010g0043others(1): Show | 4 | HG02622.hp1 HG02896.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+17292A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54845992 | ||||||
| chr18:54846111
|
C | T | 305 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(302): Show | 313 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(310): Show |
intron_variant | MODIFIER | c.-20+17411C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54846111 | ||||||
| chr18:54846132
|
T | C | 2 | a0001c0001t0002g0218a0001c0001t0002g0274 | 2 | HG02523.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-20+17432T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54846132 | ||||||
| chr18:54846139
|
A | G | 304 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(301): Show | 312 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(309): Show |
intron_variant | MODIFIER | c.-20+17439A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54846139 | ||||||
| chr18:54846145
|
G | A | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02647.hp1 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-20+17445G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54846145 | ||||||
| chr18:54846193
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-20+17493A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54846193 | ||||||
| chr18:54846217
|
C | T | 1 | a0001c0001t0014g0281 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-20+17517C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54846217 | ||||||
| chr18:54846219
|
A | G | 2 | a0001c0001t0004g0013a0001c0001t0008g0014 | 2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-20+17519A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54846219 | ||||||
| chr18:54846570
|
T | C | 305 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(302): Show | 313 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(310): Show |
intron_variant | MODIFIER | c.-20+17870T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54846570 | ||||||
| chr18:54846638
|
T | C | 25 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(22): Show | 26 | HG00438.hp1 HG00558.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.-20+17938T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54846638 | ||||||
| chr18:54846665
|
G | A | 1 | a0001c0001t0041g0305 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-20+17965G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54846665 | ||||||
| chr18:54846728
|
C | G | 1 | a0001c0001t0004g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-20+18028C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54846728 | ||||||
| chr18:54846785
|
A | T | 1 | a0001c0001t0012g0017 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-20+18085A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54846785 | ||||||
| chr18:54846954
|
G | T | 1 | a0001c0001t0033g0178 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-20+18254G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54846954 | ||||||
| chr18:54846995
|
T | C | 92 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(89): Show | 93 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.-20+18295T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54846995 | ||||||
| chr18:54847122
|
A | G | 1 | a0004c0002t0001g0315 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-20+18422A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54847122 | ||||||
| chr18:54847177
|
T | A | 91 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(88): Show | 92 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.-20+18477T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54847177 | ||||||
| chr18:54847442
|
T | C | 304 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(301): Show | 312 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(309): Show |
intron_variant | MODIFIER | c.-20+18742T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54847442 | ||||||
| chr18:54847522
|
A | G | 1 | a0001c0001t0001g0121 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-20+18822A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54847522 | ||||||
| chr18:54847612
|
T | A | 1 | a0001c0001t0001g0185 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-20+18912T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54847612 | ||||||
| chr18:54847836
|
G | A | 4 | a0001c0001t0008g0060a0001c0001t0008g0066a0001c0001t0010g0043others(1): Show | 4 | HG02622.hp1 HG02896.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+19136G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54847836 | ||||||
| chr18:54847855
|
GA | G | 211 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 218 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(215): Show |
intron_variant | MODIFIER | c.-20+19165delA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54847855 | |||||
| chr18:54847923
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-20+19223C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54847923 | ||||||
| chr18:54848017
|
A | G | 7 | a0001c0001t0006g0081a0001c0001t0006g0083a0001c0001t0006g0085others(4): Show | 7 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20+19317A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54848017 | ||||||
| chr18:54848043
|
G | A | 2 | a0001c0001t0005g0049a0001c0001t0005g0061 | 2 | HG01081.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.-20+19343G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54848043 | ||||||
| chr18:54848043
|
G | T | 1 | a0001c0001t0001g0088 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-20+19343G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54848043 | ||||||
| chr18:54848256
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-20+19556G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54848256 | ||||||
| chr18:54848311
|
A | G | 1 | a0001c0001t0002g0203 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-20+19611A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54848311 | ||||||
| chr18:54848654
|
A | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 219 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(216): Show |
intron_variant | MODIFIER | c.-20+19954A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54848654 | ||||||
| chr18:54848697
|
A | G | 1 | a0001c0001t0001g0314 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-20+19997A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54848697 | ||||||
| chr18:54848743
|
C | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(210): Show | 220 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(217): Show |
intron_variant | MODIFIER | c.-20+20043C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54848743 | ||||||
| chr18:54848810
|
A | G | 1 | a0004c0002t0001g0315 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-20+20110A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54848810 | ||||||
| chr18:54848844
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-20+20144T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54848844 | ||||||
| chr18:54849061
|
C | T | 1 | a0001c0001t0002g0268 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-20+20361C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54849061 | ||||||
| chr18:54849115
|
G | T | 1 | a0001c0001t0001g0010 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-20+20415G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54849115 | ||||||
| chr18:54849483
|
C | T | 2 | a0001c0001t0008g0060a0001c0001t0008g0066 | 2 | HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-20+20783C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54849483 | ||||||
| chr18:54849558
|
A | G | 13 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0004g0013others(10): Show | 13 | HG01109.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-20+20858A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54849558 | ||||||
| chr18:54849581
|
C | T | 2 | a0001c0001t0001g0145a0001c0001t0029g0074 | 2 | HG00673.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-20+20881C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54849581 | ||||||
| chr18:54849730
|
A | G | 7 | a0001c0001t0004g0118a0001c0001t0004g0316a0001c0001t0004g0317others(4): Show | 7 | HG02486.hp2 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20+21030A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54849730 | ||||||
| chr18:54849765
|
G | T | 1 | a0004c0002t0001g0315 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-20+21065G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54849765 | ||||||
| chr18:54849772
|
T | G | 2 | a0001c0001t0004g0103a0001c0001t0030g0104 | 2 | HG00738.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-20+21072T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54849772 | ||||||
| chr18:54849793
|
A | G | 17 | a0001c0001t0001g0009a0001c0001t0001g0307a0001c0001t0001g0308others(14): Show | 18 | HG01243.hp2 HG02055.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.-20+21093A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54849793 | ||||||
| chr18:54849920
|
T | C | 2 | a0001c0001t0010g0043a0001c0001t0030g0104 | 2 | HG00738.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-20+21220T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54849920 | ||||||
| chr18:54849980
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-20+21280C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54849980 | ||||||
| chr18:54850159
|
A | C | 3 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0299 | 3 | HG00735.hp2 HG01069.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.-20+21459A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850159 | ||||||
| chr18:54850321
|
GCAAA | G | 15 | a0001c0001t0001g0117a0001c0001t0002g0114a0001c0001t0004g0118others(12): Show | 15 | HG02055.hp1 HG02486.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-20+21628_-20+2163 others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850321 | |||||
| chr18:54850327
|
A | AGGATATA others(9): Show |
2 | a0001c0001t0006g0041a0001c0001t0006g0042 | 2 | HG01109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-20+21627_-20+2162 others(20): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850327 | ||||||
| chr18:54850329
|
A | T | 2 | a0001c0001t0006g0041a0001c0001t0006g0042 | 2 | HG01109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-20+21629A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850329 | ||||||
| chr18:54850330
|
C | A | 2 | a0001c0001t0006g0041a0001c0001t0006g0042 | 2 | HG01109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-20+21630C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850330 | ||||||
| chr18:54850331
|
A | T | 2 | a0001c0001t0006g0041a0001c0001t0006g0042 | 2 | HG01109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-20+21631A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850331 | ||||||
| chr18:54850332
|
G | A | 2 | a0001c0001t0006g0041a0001c0001t0006g0042 | 2 | HG01109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-20+21632G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850332 | ||||||
| chr18:54850333
|
G | GACATATA others(3): Show |
1 | a0001c0001t0001g0232 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-20+21634_-20+2163 others(14): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
G | GACATATA others(7): Show |
3 | a0001c0001t0001g0143a0001c0001t0001g0188a0001c0001t0001g0219 | 3 | HG00741.hp1 NA19076.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.-20+21634_-20+2163 others(18): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
G | GACATATA others(9): Show |
4 | a0001c0001t0001g0136a0001c0001t0001g0273a0001c0001t0001g0323others(1): Show | 4 | HG00558.hp2 HG00642.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+21634_-20+2163 others(20): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
G | GACATATA others(11): Show |
4 | a0001c0001t0001g0144a0001c0001t0001g0147a0001c0001t0001g0148others(1): Show | 4 | HG01978.hp1 HG02523.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+21634_-20+2163 others(22): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
G | GACATATA others(13): Show |
2 | a0001c0001t0001g0130a0001c0001t0010g0027 | 2 | NA18950.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.-20+21634_-20+2163 others(24): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
G | GACATATA others(15): Show |
9 | a0001c0001t0001g0145a0001c0001t0001g0180a0001c0001t0001g0185others(6): Show | 9 | HG00609.hp2 HG00673.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.-20+21634_-20+2163 others(26): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
G | GACATATA others(17): Show |
2 | a0001c0001t0001g0069a0001c0001t0002g0166 | 2 | HG00639.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.-20+21634_-20+2163 others(28): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
G | GACATATA others(19): Show |
10 | a0001c0001t0001g0073a0001c0001t0001g0121a0001c0001t0001g0141others(7): Show | 10 | HG01257.hp2 HG01975.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.-20+21634_-20+2163 others(30): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
G | GACATATA others(21): Show |
8 | a0001c0001t0001g0106a0001c0001t0001g0137a0001c0001t0001g0175others(5): Show | 8 | HG02004.hp2 HG02055.hp2 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+21634_-20+2163 others(32): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
G | GACATATA others(23): Show |
9 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0129others(6): Show | 10 | HG01517.hp2 HG02683.hp2 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.-20+21634_-20+2163 others(34): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
G | GACATATA others(25): Show |
12 | a0001c0001t0001g0062a0001c0001t0001g0155a0001c0001t0001g0156others(9): Show | 12 | HG01069.hp2 HG01071.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20+21634_-20+2163 others(36): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
G | GACATATA others(27): Show |
7 | a0001c0001t0001g0138a0001c0001t0001g0146a0001c0001t0001g0158others(4): Show | 7 | HG00639.hp1 HG01109.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+21634_-20+2163 others(38): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
G | GACATATA others(29): Show |
4 | a0001c0001t0001g0133a0001c0001t0002g0234a0001c0001t0003g0034others(1): Show | 4 | HG00438.hp2 HG01433.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+21634_-20+2163 others(40): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
G | GACATATA others(31): Show |
3 | a0001c0001t0001g0159a0001c0001t0001g0170a0001c0001t0003g0157 | 3 | HG01433.hp1 HG02004.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.-20+21634_-20+2163 others(42): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
G | GACATATA others(33): Show |
1 | a0001c0001t0001g0160 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-20+21634_-20+2163 others(44): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
G | GACATATA others(35): Show |
1 | a0001c0001t0010g0184 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-20+21634_-20+2163 others(46): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
G | GAT | 10 | a0001c0001t0001g0311a0001c0001t0003g0052a0001c0001t0004g0103others(7): Show | 10 | HG00738.hp1 HG01081.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.-20+21659_-20+2166 others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
G | GATATAT | 3 | a0001c0001t0002g0035a0001c0001t0018g0119a0001c0001t0028g0037 | 3 | HG01074.hp1 HG01934.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-20+21655_-20+2166 others(10): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
G | GATATATA others(3): Show |
4 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0004g0319others(1): Show | 4 | HG00099.hp1 HG01981.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+21651_-20+2166 others(14): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
G | GATATATA others(5): Show |
11 | a0001c0001t0001g0015a0001c0001t0001g0054a0001c0001t0001g0102others(8): Show | 11 | HG00558.hp1 HG01517.hp1 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.-20+21649_-20+2166 others(16): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
G | GATATATA others(7): Show |
8 | a0001c0001t0001g0026a0001c0001t0001g0079a0001c0001t0001g0229others(5): Show | 8 | HG01081.hp1 HG02109.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+21647_-20+2166 others(18): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
G | GATATATA others(9): Show |
12 | a0001c0001t0001g0030a0001c0001t0001g0076a0001c0001t0001g0100others(9): Show | 12 | HG01346.hp2 HG01934.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20+21645_-20+2166 others(20): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
G | GATATATA others(11): Show |
15 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0028others(12): Show | 15 | HG00438.hp1 HG00735.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+21643_-20+2166 others(22): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
G | GATATATA others(13): Show |
5 | a0001c0001t0001g0127a0001c0001t0001g0177a0001c0001t0001g0212others(2): Show | 5 | HG02683.hp1 HG03239.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20+21641_-20+2166 others(24): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
G | GATATATA others(15): Show |
10 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0001t0001g0217others(7): Show | 10 | HG01261.hp2 HG01346.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.-20+21639_-20+2166 others(26): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
G | GATATATA others(17): Show |
1 | a0001c0001t0006g0083 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-20+21637_-20+2166 others(28): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
G | GATATATA others(19): Show |
3 | a0001c0001t0001g0024a0001c0001t0001g0077a0001c0001t0001g0286 | 3 | HG02602.hp2 NA18959.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-20+21635_-20+2166 others(30): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
G | GATATATA others(23): Show |
2 | a0001c0001t0001g0164a0001c0001t0013g0093 | 2 | HG03491.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.-20+21660_-20+2166 others(34): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
G | GATATATA others(27): Show |
1 | a0001c0001t0001g0059 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-20+21660_-20+2166 others(38): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
G | T | 2 | a0001c0001t0006g0041a0001c0001t0006g0042 | 2 | HG01109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-20+21633G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850333 | ||||||
| chr18:54850333
|
GAT | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(99): Show | 108 | HG00609.hp1 HG00621.hp1 HG00621.hp2 others(105): Show |
intron_variant | MODIFIER | c.-20+21659_-20+2166 others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
GATATAT | G | 4 | a0001c0001t0008g0060a0001c0001t0008g0066a0001c0001t0030g0104others(1): Show | 4 | HG00738.hp2 HG02145.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+21655_-20+2166 others(10): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
GATATATA others(1): Show |
G | 13 | a0001c0001t0001g0117a0001c0001t0002g0114a0001c0001t0004g0118others(10): Show | 13 | HG02055.hp1 HG02486.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.-20+21653_-20+2166 others(12): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850333
|
GATATATA others(7): Show |
G | 2 | a0001c0001t0004g0013a0001c0001t0008g0014 | 2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-20+21647_-20+2166 others(18): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850333 | |||||
| chr18:54850335
|
T | C | 1 | a0001c0001t0001g0161 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-20+21635T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850335 | ||||||
| chr18:54850337
|
T | TATATATA others(147): Show |
1 | a0001c0001t0001g0297 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-20+21660_-20+2166 others(158): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850337 | |||||
| chr18:54850337
|
T | TATATATA others(147): Show |
1 | a0001c0001t0007g0296 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-20+21660_-20+2166 others(158): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850337 | |||||
| chr18:54850337
|
T | TATATATA others(151): Show |
1 | a0001c0001t0004g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-20+21660_-20+2166 others(162): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850337 | |||||
| chr18:54850338
|
A | G | 1 | a0001c0001t0001g0270 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-20+21638A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850338 | ||||||
| chr18:54850339
|
T | C | 2 | a0001c0001t0001g0162a0001c0001t0001g0216 | 2 | HG00099.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.-20+21639T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850339 | ||||||
| chr18:54850341
|
T | C | 1 | a0001c0001t0030g0104 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-20+21641T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850341 | ||||||
| chr18:54850353
|
T | C | 13 | a0001c0001t0001g0117a0001c0001t0002g0114a0001c0001t0004g0118others(10): Show | 13 | HG02055.hp1 HG02486.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.-20+21653T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850353 | ||||||
| chr18:54850356
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0161 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-20+21660_-20+2166 others(27): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850356 | |||||
| chr18:54850356
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0010g0190 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-20+21660_-20+2166 others(26): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850356 | |||||
| chr18:54850356
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0020g0091 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-20+21660_-20+2166 others(20): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850356 | |||||
| chr18:54850357
|
T | C | 17 | a0001c0001t0001g0117a0001c0001t0001g0179a0001c0001t0002g0114others(14): Show | 17 | HG01433.hp1 HG01496.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.-20+21657T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850357 | ||||||
| chr18:54850357
|
T | TATATATA others(27): Show |
1 | a0001c0001t0042g0109 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-20+21660_-20+2166 others(38): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850357 | |||||
| chr18:54850357
|
T | TATATATA others(41): Show |
1 | a0001c0001t0033g0178 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-20+21660_-20+2166 others(52): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850357 | |||||
| chr18:54850359
|
T | TATATATA others(7): Show |
1 | a0001c0001t0004g0111 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-20+21660_-20+2166 others(18): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850359 | |||||
| chr18:54850359
|
T | TATATATA others(151): Show |
1 | a0001c0001t0001g0295 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-20+21660_-20+2166 others(162): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850359 | |||||
| chr18:54850359
|
T | TATATATA others(7): Show |
1 | a0001c0001t0016g0107 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-20+21660_-20+2166 others(18): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850359 | |||||
| chr18:54850359
|
T | TATATATA others(15): Show |
1 | a0001c0001t0001g0113 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-20+21660_-20+2166 others(26): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850359 | |||||
| chr18:54850359
|
T | TATATATA others(13): Show |
1 | a0001c0001t0003g0002 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-20+21660_-20+2166 others(24): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850359 | |||||
| chr18:54850359
|
T | TATATATA others(19): Show |
1 | a0001c0001t0001g0031 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-20+21660_-20+2166 others(30): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850359 | |||||
| chr18:54850361
|
C | T | 11 | a0001c0001t0006g0011a0001c0001t0006g0081a0001c0001t0006g0083others(8): Show | 11 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-20+21661C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850361 | ||||||
| chr18:54850435
|
A | G | 5 | a0001c0001t0001g0065a0001c0001t0004g0013a0001c0001t0008g0004others(2): Show | 6 | HG02257.hp1 HG02976.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+21735A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850435 | ||||||
| chr18:54850559
|
G | A | 1 | a0001c0001t0008g0116 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-20+21859G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850559 | ||||||
| chr18:54850593
|
C | G | 1 | a0001c0001t0001g0025 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-20+21893C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850593 | ||||||
| chr18:54850646
|
G | A | 2 | a0001c0001t0008g0060a0001c0001t0008g0066 | 2 | HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-20+21946G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850646 | ||||||
| chr18:54850675
|
A | G | 110 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0024others(107): Show | 112 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.-20+21975A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850675 | ||||||
| chr18:54850675
|
A | T | 1 | a0001c0001t0010g0123 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-20+21975A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850675 | ||||||
| chr18:54850736
|
CT | C | 3 | a0001c0001t0018g0119a0001c0001t0040g0194a0003c0003t0031g0108 | 3 | HG02145.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-20+22040delT | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54850736 | |||||
| chr18:54850765
|
A | G | 1 | a0001c0001t0010g0190 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-20+22065A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850765 | ||||||
| chr18:54850865
|
T | C | 3 | a0001c0001t0001g0230a0001c0001t0017g0151a0001c0001t0017g0173 | 3 | NA18961.hp2 NA18974.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-20+22165T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850865 | ||||||
| chr18:54850874
|
G | T | 3 | a0001c0001t0018g0119a0001c0001t0040g0194a0003c0003t0031g0108 | 3 | HG02145.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-20+22174G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850874 | ||||||
| chr18:54850886
|
A | G | 1 | a0001c0001t0043g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-20+22186A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850886 | ||||||
| chr18:54850925
|
G | T | 6 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(3): Show | 6 | HG00438.hp1 HG03831.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+22225G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54850925 | ||||||
| chr18:54851013
|
T | C | 1 | a0001c0001t0002g0226 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-20+22313T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54851013 | ||||||
| chr18:54851134
|
A | G | 2 | a0001c0001t0004g0110a0001c0001t0029g0074 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-20+22434A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54851134 | ||||||
| chr18:54851216
|
A | G | 1 | a0001c0001t0010g0190 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-20+22516A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54851216 | ||||||
| chr18:54851275
|
C | T | 2 | a0001c0001t0004g0013a0001c0001t0008g0014 | 2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-20+22575C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54851275 | ||||||
| chr18:54851426
|
T | G | 1 | a0001c0001t0018g0134 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-20+22726T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54851426 | ||||||
| chr18:54851652
|
C | A | 2 | a0001c0001t0014g0050a0001c0001t0014g0281 | 2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-20+22952C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54851652 | ||||||
| chr18:54851748
|
C | A | 5 | a0001c0001t0001g0224a0001c0001t0001g0253a0001c0001t0001g0254others(2): Show | 5 | NA18942.hp2 NA18990.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20+23048C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54851748 | ||||||
| chr18:54851831
|
A | C | 3 | a0001c0001t0018g0119a0001c0001t0040g0194a0003c0003t0031g0108 | 3 | HG02145.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-20+23131A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54851831 | ||||||
| chr18:54852020
|
C | T | 2 | a0001c0001t0001g0113a0001c0001t0002g0114 | 2 | HG02818.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-20+23320C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54852020 | ||||||
| chr18:54852152
|
C | T | 1 | a0001c0001t0008g0004 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-20+23452C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54852152 | ||||||
| chr18:54852380
|
T | G | 1 | a0001c0001t0003g0078 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-20+23680T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54852380 | ||||||
| chr18:54852554
|
C | A | 2 | a0001c0001t0004g0067a0001c0001t0004g0103 | 2 | HG02622.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-20+23854C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54852554 | ||||||
| chr18:54852620
|
A | G | 1 | a0001c0001t0002g0226 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-20+23920A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54852620 | ||||||
| chr18:54852743
|
A | G | 1 | a0001c0001t0002g0223 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-20+24043A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54852743 | ||||||
| chr18:54852854
|
G | T | 1 | a0001c0001t0019g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-20+24154G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54852854 | ||||||
| chr18:54852918
|
C | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(179): Show | 188 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(185): Show |
intron_variant | MODIFIER | c.-20+24218C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54852918 | ||||||
| chr18:54852945
|
T | G | 4 | a0001c0001t0004g0067a0001c0001t0004g0103a0001c0001t0018g0134others(1): Show | 4 | HG00738.hp2 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+24245T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54852945 | ||||||
| chr18:54853053
|
A | G | 2 | a0001c0001t0001g0065a0001c0001t0001g0072 | 2 | HG00735.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-20+24353A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54853053 | ||||||
| chr18:54853153
|
G | A | 1 | a0001c0001t0043g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19-24414G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54853153 | ||||||
| chr18:54853185
|
G | A | 94 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0069others(91): Show | 96 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.-19-24382G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54853185 | ||||||
| chr18:54853449
|
A | C | 288 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(285): Show | 295 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(292): Show |
intron_variant | MODIFIER | c.-19-24118A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54853449 | ||||||
| chr18:54853784
|
G | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(67): Show | 74 | HG00099.hp1 HG00609.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.-19-23783G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54853784 | ||||||
| chr18:54853856
|
C | T | 4 | a0001c0001t0002g0195a0001c0001t0002g0222a0001c0001t0002g0251others(1): Show | 4 | HG00642.hp2 HG01358.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-23711C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54853856 | ||||||
| chr18:54854138
|
T | G | 2 | a0001c0001t0008g0060a0001c0001t0008g0066 | 2 | HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-19-23429T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54854138 | ||||||
| chr18:54854303
|
G | A | 24 | a0001c0001t0001g0055a0001c0001t0001g0167a0001c0001t0001g0168others(21): Show | 25 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-19-23264G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54854303 | ||||||
| chr18:54854492
|
G | T | 1 | a0001c0001t0038g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-19-23075G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54854492 | ||||||
| chr18:54854567
|
A | G | 2 | a0001c0001t0002g0075a0001c0001t0002g0250 | 2 | HG01099.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-19-23000A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54854567 | ||||||
| chr18:54854577
|
G | A | 1 | a0001c0001t0015g0016 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-19-22990G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54854577 | ||||||
| chr18:54854609
|
A | G | 1 | a0001c0001t0008g0082 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-19-22958A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54854609 | ||||||
| chr18:54854743
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-19-22824A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54854743 | ||||||
| chr18:54854912
|
G | C | 2 | a0001c0001t0004g0110a0001c0001t0029g0074 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-22655G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54854912 | ||||||
| chr18:54854929
|
C | T | 2 | a0001c0001t0004g0110a0001c0001t0029g0074 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-22638C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54854929 | ||||||
| chr18:54854951
|
A | G | 2 | a0001c0001t0008g0014a0001c0001t0019g0040 | 2 | HG01891.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-19-22616A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54854951 | ||||||
| chr18:54855058
|
C | T | 16 | a0001c0001t0001g0009a0001c0001t0001g0295a0001c0001t0001g0307others(13): Show | 17 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-19-22509C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855058 | ||||||
| chr18:54855094
|
C | T | 16 | a0001c0001t0001g0009a0001c0001t0001g0295a0001c0001t0001g0307others(13): Show | 17 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-19-22473C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855094 | ||||||
| chr18:54855133
|
G | A | 15 | a0001c0001t0001g0009a0001c0001t0001g0295a0001c0001t0001g0307others(12): Show | 16 | HG01243.hp2 HG02145.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-19-22434G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855133 | ||||||
| chr18:54855170
|
G | T | 2 | a0001c0001t0008g0014a0001c0001t0019g0040 | 2 | HG01891.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-19-22397G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855170 | ||||||
| chr18:54855220
|
T | C | 307 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(304): Show | 315 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(312): Show |
intron_variant | MODIFIER | c.-19-22347T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855220 | ||||||
| chr18:54855221
|
G | A | 2 | a0001c0001t0004g0110a0001c0001t0029g0074 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-22346G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855221 | ||||||
| chr18:54855232
|
G | A | 1 | a0001c0001t0008g0014 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-19-22335G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855232 | ||||||
| chr18:54855305
|
C | T | 2 | a0001c0001t0014g0050a0001c0001t0014g0281 | 2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-19-22262C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855305 | ||||||
| chr18:54855332
|
C | T | 1 | a0001c0001t0001g0161 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-19-22235C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855332 | ||||||
| chr18:54855429
|
A | G | 1 | a0001c0001t0022g0095 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-19-22138A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855429 | ||||||
| chr18:54855444
|
T | G | 1 | a0001c0001t0043g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19-22123T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855444 | ||||||
| chr18:54855495
|
A | G | 1 | a0001c0001t0002g0186 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-19-22072A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855495 | ||||||
| chr18:54855502
|
A | G | 306 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(303): Show | 314 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(311): Show |
intron_variant | MODIFIER | c.-19-22065A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855502 | ||||||
| chr18:54855512
|
G | A | 2 | a0001c0001t0002g0235a0001c0001t0002g0236 | 2 | NA18985.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.-19-22055G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855512 | ||||||
| chr18:54855516
|
T | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(73): Show | 80 | HG00099.hp1 HG00609.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.-19-22051T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855516 | ||||||
| chr18:54855587
|
G | A | 2 | a0001c0001t0001g0212a0001c0001t0001g0217 | 2 | NA18966.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-19-21980G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855587 | ||||||
| chr18:54855610
|
C | T | 82 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0069others(79): Show | 84 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.-19-21957C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855610 | ||||||
| chr18:54855802
|
C | G | 1 | a0001c0001t0002g0249 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-19-21765C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855802 | ||||||
| chr18:54855850
|
G | T | 2 | a0001c0001t0008g0014a0001c0001t0019g0040 | 2 | HG01891.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-19-21717G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855850 | ||||||
| chr18:54855899
|
T | C | 1 | a0001c0001t0018g0134 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-19-21668T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855899 | ||||||
| chr18:54855900
|
C | T | 2 | a0001c0001t0004g0110a0001c0001t0029g0074 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-21667C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54855900 | ||||||
| chr18:54856147
|
G | T | 1 | a0001c0001t0034g0310 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-19-21420G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54856147 | ||||||
| chr18:54856206
|
T | C | 103 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0024others(100): Show | 104 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.-19-21361T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54856206 | ||||||
| chr18:54856230
|
T | G | 8 | a0001c0001t0001g0045a0001c0001t0001g0054a0001c0001t0001g0076others(5): Show | 8 | HG02602.hp2 HG02683.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19-21337T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54856230 | ||||||
| chr18:54856246
|
G | A | 82 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0069others(79): Show | 84 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.-19-21321G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54856246 | ||||||
| chr18:54856541
|
G | A | 3 | a0001c0001t0018g0119a0001c0001t0040g0194a0003c0003t0031g0108 | 3 | HG02145.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-19-21026G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54856541 | ||||||
| chr18:54856759
|
A | G | 1 | a0001c0001t0030g0104 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-19-20808A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54856759 | ||||||
| chr18:54857005
|
C | T | 5 | a0001c0001t0003g0053a0001c0001t0003g0058a0001c0001t0003g0078others(2): Show | 5 | HG00639.hp1 HG02602.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-20562C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54857005 | ||||||
| chr18:54857077
|
A | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(74): Show | 81 | HG00099.hp1 HG00609.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.-19-20490A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54857077 | ||||||
| chr18:54857253
|
C | A | 3 | a0001c0001t0002g0007a0001c0001t0002g0223a0001c0001t0002g0268 | 4 | HG00673.hp1 HG02129.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-20314C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54857253 | ||||||
| chr18:54857348
|
A | G | 12 | a0001c0001t0001g0009a0001c0001t0001g0295a0001c0001t0001g0307others(9): Show | 13 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-20219A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54857348 | ||||||
| chr18:54857453
|
C | T | 1 | a0003c0003t0031g0108 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-19-20114C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54857453 | ||||||
| chr18:54857520
|
C | T | 1 | a0001c0001t0002g0287 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-19-20047C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54857520 | ||||||
| chr18:54857601
|
A | G | 2 | a0001c0001t0014g0050a0001c0001t0014g0281 | 2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-19-19966A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54857601 | ||||||
| chr18:54857623
|
C | G | 2 | a0001c0001t0004g0067a0001c0001t0004g0103 | 2 | HG02622.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-19-19944C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54857623 | ||||||
| chr18:54857683
|
C | T | 1 | a0001c0001t0026g0322 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-19-19884C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54857683 | ||||||
| chr18:54857729
|
CA | C | 16 | a0001c0001t0001g0009a0001c0001t0001g0295a0001c0001t0001g0307others(13): Show | 17 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-19-19836delA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54857729 | |||||
| chr18:54857787
|
A | G | 1 | a0001c0001t0042g0109 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-19-19780A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54857787 | ||||||
| chr18:54857864
|
C | A | 2 | a0001c0001t0004g0110a0001c0001t0029g0074 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-19703C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54857864 | ||||||
| chr18:54857967
|
T | C | 1 | a0001c0001t0009g0094 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-19-19600T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54857967 | ||||||
| chr18:54858016
|
T | G | 82 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0030others(79): Show | 83 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.-19-19551T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858016 | ||||||
| chr18:54858126
|
C | T | 3 | a0001c0001t0018g0119a0001c0001t0040g0194a0003c0003t0031g0108 | 3 | HG02145.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-19-19441C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858126 | ||||||
| chr18:54858347
|
A | G | 1 | a0001c0001t0043g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19-19220A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858347 | ||||||
| chr18:54858354
|
G | T | 1 | a0001c0001t0043g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19-19213G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858354 | ||||||
| chr18:54858357
|
C | T | 1 | a0001c0001t0018g0134 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-19-19210C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858357 | ||||||
| chr18:54858377
|
GT | G | 111 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(108): Show | 113 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.-19-19165delT | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54858377 | |||||
| chr18:54858377
|
GTT | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 187 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(184): Show |
intron_variant | MODIFIER | c.-19-19166_-19-1916 others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54858377 | |||||
| chr18:54858377
|
GTTTTTTT others(5): Show |
G | 2 | a0001c0001t0004g0067a0001c0001t0004g0103 | 2 | HG02622.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-19-19176_-19-1916 others(16): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54858377 | |||||
| chr18:54858385
|
T | G | 13 | a0001c0001t0001g0022a0001c0001t0001g0031a0001c0001t0002g0165others(10): Show | 13 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19-19182T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858385 | ||||||
| chr18:54858386
|
T | G | 107 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(104): Show | 109 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.-19-19181T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858386 | ||||||
| chr18:54858387
|
T | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 187 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(184): Show |
intron_variant | MODIFIER | c.-19-19180T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858387 | ||||||
| chr18:54858390
|
T | G | 1 | a0001c0001t0030g0104 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-19-19177T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858390 | ||||||
| chr18:54858477
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0009g0098 | 2 | HG03704.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-19-19090C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858477 | ||||||
| chr18:54858517
|
GGGACTA | G | 4 | a0001c0001t0005g0048a0001c0001t0005g0049a0001c0001t0005g0051others(1): Show | 4 | HG00738.hp1 HG01081.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-19049_-19-1904 others(10): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858517 | ||||||
| chr18:54858524
|
C | T | 4 | a0001c0001t0005g0048a0001c0001t0005g0049a0001c0001t0005g0051others(1): Show | 4 | HG00738.hp1 HG01081.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-19043C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858524 | ||||||
| chr18:54858527
|
G | T | 4 | a0001c0001t0005g0048a0001c0001t0005g0049a0001c0001t0005g0051others(1): Show | 4 | HG00738.hp1 HG01081.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-19040G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858527 | ||||||
| chr18:54858528
|
T | C | 4 | a0001c0001t0005g0048a0001c0001t0005g0049a0001c0001t0005g0051others(1): Show | 4 | HG00738.hp1 HG01081.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-19039T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858528 | ||||||
| chr18:54858544
|
C | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(74): Show | 81 | HG00099.hp1 HG00609.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.-19-19023C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858544 | ||||||
| chr18:54858581
|
G | A | 2 | a0001c0001t0004g0110a0001c0001t0029g0074 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-18986G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858581 | ||||||
| chr18:54858622
|
G | A | 1 | a0001c0001t0043g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19-18945G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858622 | ||||||
| chr18:54858817
|
A | G | 3 | a0001c0001t0002g0248a0001c0001t0002g0280a0001c0001t0002g0287 | 3 | HG01257.hp1 HG01258.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-19-18750A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858817 | ||||||
| chr18:54858832
|
A | G | 2 | a0001c0001t0004g0110a0001c0001t0029g0074 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-18735A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858832 | ||||||
| chr18:54858857
|
G | A | 1 | a0001c0001t0001g0026 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-19-18710G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858857 | ||||||
| chr18:54858894
|
A | G | 1 | a0001c0001t0030g0104 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-19-18673A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858894 | ||||||
| chr18:54858940
|
T | C | 1 | a0001c0001t0003g0038 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-19-18627T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54858940 | ||||||
| chr18:54859098
|
C | T | 2 | a0001c0001t0004g0110a0001c0001t0029g0074 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-18469C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54859098 | ||||||
| chr18:54859203
|
A | C | 1 | a0001c0001t0001g0117 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-19-18364A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54859203 | ||||||
| chr18:54859207
|
G | A | 1 | a0001c0001t0045g0039 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-19-18360G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54859207 | ||||||
| chr18:54859406
|
C | T | 1 | a0001c0001t0003g0002 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-19-18161C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54859406 | ||||||
| chr18:54859486
|
C | CA | 18 | a0001c0001t0001g0056a0001c0001t0001g0059a0001c0001t0001g0079others(15): Show | 18 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.-19-18066dupA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54859486 | |||||
| chr18:54859486
|
CA | C | 38 | a0001c0001t0001g0071a0001c0001t0001g0100a0001c0001t0001g0102others(35): Show | 38 | HG00738.hp1 HG01070.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-19-18066delA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54859486 | |||||
| chr18:54859486
|
CAA | C | 67 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0030others(64): Show | 68 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.-19-18067_-19-1806 others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54859486 | |||||
| chr18:54859511
|
C | T | 1 | a0001c0001t0002g0246 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-19-18056C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54859511 | ||||||
| chr18:54859740
|
A | T | 2 | a0001c0001t0008g0116a0001c0001t0033g0178 | 2 | HG02486.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-19-17827A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54859740 | ||||||
| chr18:54859753
|
G | A | 1 | a0001c0001t0002g0191 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-19-17814G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54859753 | ||||||
| chr18:54859839
|
C | T | 269 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(266): Show | 274 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(271): Show |
intron_variant | MODIFIER | c.-19-17728C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54859839 | ||||||
| chr18:54859990
|
A | T | 1 | a0001c0001t0019g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-19-17577A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54859990 | ||||||
| chr18:54860068
|
T | G | 104 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0024others(101): Show | 105 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.-19-17499T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54860068 | ||||||
| chr18:54860075
|
A | T | 1 | a0001c0001t0018g0134 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-19-17492A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54860075 | ||||||
| chr18:54860085
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-19-17482T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54860085 | ||||||
| chr18:54860234
|
T | C | 84 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0030others(81): Show | 85 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.-19-17333T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54860234 | ||||||
| chr18:54860655
|
T | C | 1 | a0004c0002t0001g0315 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-19-16912T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54860655 | ||||||
| chr18:54860760
|
A | T | 2 | a0001c0001t0002g0228a0001c0001t0002g0262 | 2 | NA18959.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-19-16807A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54860760 | ||||||
| chr18:54860903
|
T | C | 3 | a0001c0001t0001g0142a0001c0001t0002g0008a0001c0001t0002g0237 | 4 | HG01358.hp1 HG01978.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-16664T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54860903 | ||||||
| chr18:54860906
|
C | A | 1 | a0001c0001t0043g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19-16661C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54860906 | ||||||
| chr18:54861110
|
T | C | 1 | a0001c0001t0002g0258 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-19-16457T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54861110 | ||||||
| chr18:54861142
|
T | C | 1 | a0001c0001t0002g0271 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-19-16425T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54861142 | ||||||
| chr18:54861304
|
T | C | 1 | a0001c0001t0040g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-19-16263T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54861304 | ||||||
| chr18:54861304
|
T | G | 1 | a0001c0001t0001g0230 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-19-16263T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54861304 | ||||||
| chr18:54861313
|
A | T | 2 | a0001c0001t0004g0110a0001c0001t0029g0074 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-16254A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54861313 | ||||||
| chr18:54861457
|
G | A | 81 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0018others(78): Show | 82 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.-19-16110G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54861457 | ||||||
| chr18:54861494
|
C | T | 2 | a0001c0001t0004g0067a0001c0001t0004g0103 | 2 | HG02622.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-19-16073C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54861494 | ||||||
| chr18:54861548
|
A | G | 1 | a0001c0001t0043g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19-16019A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54861548 | ||||||
| chr18:54861618
|
G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0015others(73): Show | 80 | HG00099.hp1 HG00609.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.-19-15949G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54861618 | ||||||
| chr18:54861704
|
C | T | 1 | a0001c0001t0002g0075 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-19-15863C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54861704 | ||||||
| chr18:54861731
|
G | T | 1 | a0001c0001t0012g0017 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-19-15836G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54861731 | ||||||
| chr18:54861739
|
A | G | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0216 | 3 | HG00099.hp2 HG01106.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-19-15828A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54861739 | ||||||
| chr18:54861847
|
A | G | 8 | a0001c0001t0001g0009a0001c0001t0001g0295a0001c0001t0001g0307others(5): Show | 9 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19-15720A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54861847 | ||||||
| chr18:54861897
|
T | C | 1 | a0001c0001t0043g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19-15670T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54861897 | ||||||
| chr18:54861920
|
A | G | 1 | a0001c0001t0043g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19-15647A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54861920 | ||||||
| chr18:54862005
|
T | C | 1 | a0001c0001t0008g0014 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-19-15562T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54862005 | ||||||
| chr18:54862059
|
GA | G | 279 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 286 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(283): Show |
intron_variant | MODIFIER | c.-19-15496delA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54862059 | |||||
| chr18:54862059
|
GAA | G | 8 | a0001c0001t0004g0110a0001c0001t0008g0004a0001c0001t0008g0014others(5): Show | 9 | HG01891.hp1 HG02258.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-15497_-19-1549 others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54862059 | |||||
| chr18:54862237
|
T | C | 1 | a0001c0001t0008g0014 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-19-15330T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54862237 | ||||||
| chr18:54862398
|
A | C | 2 | a0001c0001t0001g0113a0001c0001t0002g0114 | 2 | HG02818.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-19-15169A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54862398 | ||||||
| chr18:54862401
|
G | A | 8 | a0001c0001t0004g0110a0001c0001t0008g0004a0001c0001t0008g0014others(5): Show | 9 | HG01891.hp1 HG02258.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-15166G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54862401 | ||||||
| chr18:54862491
|
G | T | 1 | a0001c0001t0001g0171 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-19-15076G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54862491 | ||||||
| chr18:54862787
|
G | A | 91 | a0001c0001t0001g0031a0001c0001t0001g0062a0001c0001t0001g0069others(88): Show | 93 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.-19-14780G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54862787 | ||||||
| chr18:54862910
|
T | A | 1 | a0001c0001t0043g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19-14657T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54862910 | ||||||
| chr18:54862915
|
G | T | 1 | a0001c0001t0010g0313 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-19-14652G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54862915 | ||||||
| chr18:54862928
|
T | G | 2 | a0001c0001t0006g0041a0001c0001t0006g0042 | 2 | HG01109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-19-14639T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54862928 | ||||||
| chr18:54863154
|
G | C | 94 | a0001c0001t0001g0031a0001c0001t0001g0054a0001c0001t0001g0062others(91): Show | 96 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.-19-14413G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54863154 | ||||||
| chr18:54863174
|
A | G | 75 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0015others(72): Show | 79 | HG00099.hp1 HG00609.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.-19-14393A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54863174 | ||||||
| chr18:54863182
|
T | C | 1 | a0001c0001t0043g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19-14385T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54863182 | ||||||
| chr18:54863183
|
G | A | 311 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(308): Show | 320 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(317): Show |
intron_variant | MODIFIER | c.-19-14384G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54863183 | ||||||
| chr18:54863208
|
G | T | 1 | a0001c0001t0002g0272 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-19-14359G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54863208 | ||||||
| chr18:54863453
|
A | G | 2 | a0001c0001t0002g0244a0001c0001t0002g0276 | 2 | HG02083.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.-19-14114A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54863453 | ||||||
| chr18:54863570
|
T | A | 2 | a0001c0001t0006g0041a0001c0001t0006g0042 | 2 | HG01109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-19-13997T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54863570 | ||||||
| chr18:54863583
|
C | A | 1 | a0001c0001t0003g0053 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-19-13984C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54863583 | ||||||
| chr18:54863647
|
G | A | 311 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(308): Show | 320 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(317): Show |
intron_variant | MODIFIER | c.-19-13920G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54863647 | ||||||
| chr18:54863766
|
A | T | 311 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(308): Show | 320 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(317): Show |
intron_variant | MODIFIER | c.-19-13801A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54863766 | ||||||
| chr18:54863967
|
T | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0015others(169): Show | 178 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(175): Show |
intron_variant | MODIFIER | c.-19-13600T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54863967 | ||||||
| chr18:54863977
|
T | C | 6 | a0001c0001t0008g0004a0001c0001t0008g0014a0001c0001t0008g0060others(3): Show | 7 | HG01891.hp1 HG02622.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-13590T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54863977 | ||||||
| chr18:54864136
|
A | AGGAG | 13 | a0001c0001t0001g0009a0001c0001t0001g0295a0001c0001t0001g0307others(10): Show | 14 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-19-13428_-19-1342 others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54864136 | |||||
| chr18:54864280
|
C | T | 1 | a0001c0001t0002g0234 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-19-13287C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54864280 | ||||||
| chr18:54864496
|
A | T | 1 | a0001c0001t0001g0210 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-19-13071A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54864496 | ||||||
| chr18:54864496
|
AT | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0015others(70): Show | 77 | HG00099.hp1 HG00609.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.-19-13062delT | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54864496 | |||||
| chr18:54864931
|
G | T | 8 | a0001c0001t0004g0110a0001c0001t0008g0004a0001c0001t0008g0014others(5): Show | 9 | HG01891.hp1 HG02258.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-12636G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54864931 | ||||||
| chr18:54864943
|
G | C | 20 | a0001c0001t0001g0009a0001c0001t0001g0295a0001c0001t0001g0307others(17): Show | 22 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19-12624G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54864943 | ||||||
| chr18:54864976
|
G | C | 1 | a0001c0001t0003g0058 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-19-12591G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54864976 | ||||||
| chr18:54865031
|
A | T | 2 | a0001c0001t0004g0067a0001c0001t0004g0103 | 2 | HG02622.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-19-12536A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865031 | ||||||
| chr18:54865089
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-19-12478A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865089 | ||||||
| chr18:54865184
|
C | T | 1 | a0001c0001t0018g0134 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-19-12383C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865184 | ||||||
| chr18:54865200
|
T | A | 1 | a0001c0001t0002g0204 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-19-12367T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865200 | ||||||
| chr18:54865232
|
G | T | 1 | a0001c0001t0019g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-19-12335G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865232 | ||||||
| chr18:54865237
|
T | TTG | 75 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0018others(72): Show | 76 | HG00099.hp2 HG00558.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.-19-12294_-19-1229 others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54865237 | |||||
| chr18:54865237
|
T | TTGTG | 43 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(40): Show | 43 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.-19-12296_-19-1229 others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54865237 | |||||
| chr18:54865237
|
T | TTGTGTG | 27 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0036others(24): Show | 30 | HG00673.hp2 HG01081.hp1 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.-19-12298_-19-1229 others(10): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54865237 | |||||
| chr18:54865237
|
T | TTGTGTGT others(1): Show |
30 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(27): Show | 31 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.-19-12300_-19-1229 others(12): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54865237 | |||||
| chr18:54865237
|
T | TTGTGTGT others(3): Show |
7 | a0001c0001t0001g0100a0001c0001t0001g0125a0001c0001t0003g0053others(4): Show | 7 | HG00099.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-12302_-19-1229 others(14): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54865237 | |||||
| chr18:54865237
|
T | TTGTGTGT others(5): Show |
4 | a0001c0001t0003g0058a0001c0001t0003g0154a0001c0001t0003g0157others(1): Show | 4 | HG01433.hp1 HG01496.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-12304_-19-1229 others(16): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54865237 | |||||
| chr18:54865237
|
TTG | T | 13 | a0001c0001t0001g0138a0001c0001t0001g0153a0001c0001t0001g0175others(10): Show | 13 | HG00621.hp1 HG01109.hp2 HG02965.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-12294_-19-1229 others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54865237 | |||||
| chr18:54865237
|
TTGTG | T | 95 | a0001c0001t0001g0009a0001c0001t0001g0031a0001c0001t0001g0054others(92): Show | 99 | HG00558.hp1 HG00639.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.-19-12296_-19-1229 others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54865237 | |||||
| chr18:54865237
|
TTGTGTG | T | 5 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0002g0191others(2): Show | 5 | HG01069.hp1 HG01074.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19-12298_-19-1229 others(10): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54865237 | |||||
| chr18:54865355
|
C | A | 311 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(308): Show | 320 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(317): Show |
intron_variant | MODIFIER | c.-19-12212C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865355 | ||||||
| chr18:54865379
|
TC | T | 8 | a0001c0001t0004g0110a0001c0001t0008g0004a0001c0001t0008g0014others(5): Show | 9 | HG01891.hp1 HG02258.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-12187delC | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865379 | ||||||
| chr18:54865403
|
T | C | 98 | a0001c0001t0001g0031a0001c0001t0001g0054a0001c0001t0001g0062others(95): Show | 100 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.-19-12164T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865403 | ||||||
| chr18:54865427
|
A | T | 1 | a0001c0001t0001g0324 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-19-12140A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865427 | ||||||
| chr18:54865529
|
T | C | 1 | a0001c0001t0008g0004 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-19-12038T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865529 | ||||||
| chr18:54865672
|
C | T | 8 | a0001c0001t0004g0110a0001c0001t0008g0004a0001c0001t0008g0014others(5): Show | 9 | HG01891.hp1 HG02258.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-11895C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865672 | ||||||
| chr18:54865737
|
A | G | 8 | a0001c0001t0004g0110a0001c0001t0008g0004a0001c0001t0008g0014others(5): Show | 9 | HG01891.hp1 HG02258.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-11830A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865737 | ||||||
| chr18:54865739
|
T | A | 8 | a0001c0001t0004g0110a0001c0001t0008g0004a0001c0001t0008g0014others(5): Show | 9 | HG01891.hp1 HG02258.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-11828T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865739 | ||||||
| chr18:54865779
|
A | G | 46 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0015others(43): Show | 50 | HG00609.hp1 HG00673.hp2 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.-19-11788A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865779 | ||||||
| chr18:54865807
|
C | T | 90 | a0001c0001t0001g0031a0001c0001t0001g0062a0001c0001t0001g0069others(87): Show | 92 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.-19-11760C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865807 | ||||||
| chr18:54865845
|
T | G | 310 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(307): Show | 319 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(316): Show |
intron_variant | MODIFIER | c.-19-11722T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865845 | ||||||
| chr18:54865860
|
A | G | 1 | a0001c0001t0002g0236 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-19-11707A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865860 | ||||||
| chr18:54865946
|
A | C | 37 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0015others(34): Show | 40 | HG00609.hp1 HG00673.hp2 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.-19-11621A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865946 | ||||||
| chr18:54865959
|
G | T | 1 | a0001c0001t0008g0014 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-19-11608G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54865959 | ||||||
| chr18:54866095
|
CA | C | 12 | a0001c0001t0001g0009a0001c0001t0001g0295a0001c0001t0001g0307others(9): Show | 13 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-11462delA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54866095 | |||||
| chr18:54866105
|
AC | A | 8 | a0001c0001t0004g0110a0001c0001t0008g0004a0001c0001t0008g0014others(5): Show | 9 | HG01891.hp1 HG02258.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-11461delC | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54866105 | ||||||
| chr18:54866108
|
G | C | 8 | a0001c0001t0004g0110a0001c0001t0008g0004a0001c0001t0008g0014others(5): Show | 9 | HG01891.hp1 HG02258.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-11459G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54866108 | ||||||
| chr18:54866149
|
G | A | 1 | a0001c0001t0018g0134 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-19-11418G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54866149 | ||||||
| chr18:54866221
|
T | A | 96 | a0001c0001t0001g0031a0001c0001t0001g0054a0001c0001t0001g0062others(93): Show | 98 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.-19-11346T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54866221 | ||||||
| chr18:54866263
|
TCCTCCCC others(1): Show |
T | 75 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0015others(72): Show | 79 | HG00099.hp1 HG00609.hp1 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.-19-11285_-19-1127 others(12): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54866263 | |||||
| chr18:54866299
|
C | T | 2 | a0001c0001t0014g0050a0001c0001t0014g0281 | 2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-19-11268C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54866299 | ||||||
| chr18:54866306
|
T | C | 12 | a0001c0001t0001g0009a0001c0001t0001g0295a0001c0001t0001g0307others(9): Show | 13 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-11261T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54866306 | ||||||
| chr18:54866372
|
C | T | 19 | a0001c0001t0001g0009a0001c0001t0001g0295a0001c0001t0001g0308others(16): Show | 21 | HG01891.hp1 HG02258.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.-19-11195C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54866372 | ||||||
| chr18:54866381
|
C | T | 3 | a0001c0001t0007g0046a0001c0001t0013g0092a0001c0001t0013g0093 | 3 | HG01261.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-19-11186C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54866381 | ||||||
| chr18:54866457
|
G | A | 12 | a0001c0001t0001g0009a0001c0001t0001g0295a0001c0001t0001g0307others(9): Show | 13 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-11110G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54866457 | ||||||
| chr18:54866532
|
A | G | 1 | a0001c0001t0001g0293 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-19-11035A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54866532 | ||||||
| chr18:54866645
|
C | A | 1 | a0001c0001t0004g0110 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-19-10922C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54866645 | ||||||
| chr18:54866850
|
G | A | 6 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(3): Show | 6 | HG00438.hp1 HG03831.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19-10717G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54866850 | ||||||
| chr18:54866985
|
C | A | 1 | a0001c0001t0018g0134 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-19-10582C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54866985 | ||||||
| chr18:54867018
|
C | G | 1 | a0001c0001t0042g0109 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-19-10549C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867018 | ||||||
| chr18:54867038
|
G | T | 12 | a0001c0001t0001g0009a0001c0001t0001g0295a0001c0001t0001g0307others(9): Show | 13 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-10529G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867038 | ||||||
| chr18:54867063
|
G | T | 1 | a0001c0001t0002g0241 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-19-10504G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867063 | ||||||
| chr18:54867231
|
G | C | 12 | a0001c0001t0001g0009a0001c0001t0001g0295a0001c0001t0001g0307others(9): Show | 13 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-10336G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867231 | ||||||
| chr18:54867256
|
C | T | 1 | a0001c0001t0002g0195 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-19-10311C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867256 | ||||||
| chr18:54867438
|
T | A | 1 | a0001c0001t0001g0117 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-19-10129T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867438 | ||||||
| chr18:54867442
|
C | CT | 100 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0054others(97): Show | 102 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.-19-10105dupT | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54867442 | |||||
| chr18:54867442
|
C | CTT | 8 | a0001c0001t0001g0323a0001c0001t0002g0213a0001c0001t0002g0241others(5): Show | 8 | HG00642.hp1 HG00738.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19-10106_-19-1010 others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54867442 | |||||
| chr18:54867442
|
C | CTTTTCT | 69 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0015others(66): Show | 73 | HG00099.hp1 HG00609.hp1 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.-19-10121_-19-1012 others(10): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54867442 | |||||
| chr18:54867442
|
C | CTTTTCTT others(4): Show |
1 | a0001c0001t0003g0078 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-19-10121_-19-1012 others(15): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54867442 | |||||
| chr18:54867445
|
T | TTC | 74 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0018others(71): Show | 75 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.-19-10121_-19-1012 others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54867445 | |||||
| chr18:54867446
|
T | TC | 8 | a0001c0001t0001g0293a0001c0001t0008g0004a0001c0001t0008g0014others(5): Show | 9 | HG01891.hp1 HG02622.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-10121_-19-1012 others(5): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867446 | ||||||
| chr18:54867446
|
T | TCTTTTCT others(19): Show |
2 | a0001c0001t0004g0110a0001c0001t0029g0074 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-10121_-19-1012 others(30): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867446 | ||||||
| chr18:54867447
|
T | C | 12 | a0001c0001t0001g0009a0001c0001t0001g0295a0001c0001t0001g0307others(9): Show | 13 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-10120T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867447 | ||||||
| chr18:54867456
|
T | G | 12 | a0001c0001t0001g0009a0001c0001t0001g0295a0001c0001t0001g0307others(9): Show | 13 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-10111T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867456 | ||||||
| chr18:54867549
|
C | T | 1 | a0001c0001t0043g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19-10018C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867549 | ||||||
| chr18:54867718
|
T | C | 1 | a0001c0001t0016g0107 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-19-9849T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867718 | ||||||
| chr18:54867725
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0002g0114 | 2 | HG02818.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-19-9842G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867725 | ||||||
| chr18:54867740
|
C | T | 1 | a0001c0001t0030g0104 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-19-9827C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867740 | ||||||
| chr18:54867792
|
G | T | 1 | a0001c0001t0042g0109 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-19-9775G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867792 | ||||||
| chr18:54867834
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-19-9733A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867834 | ||||||
| chr18:54867966
|
G | A | 72 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0015others(69): Show | 76 | HG00099.hp1 HG00609.hp1 HG00673.hp2 others(73): Show |
intron_variant | MODIFIER | c.-19-9601G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867966 | ||||||
| chr18:54867973
|
T | G | 12 | a0001c0001t0001g0009a0001c0001t0001g0295a0001c0001t0001g0307others(9): Show | 13 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-9594T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54867973 | ||||||
| chr18:54868066
|
T | C | 1 | a0001c0001t0020g0091 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-19-9501T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54868066 | ||||||
| chr18:54868138
|
G | C | 2 | a0001c0001t0014g0050a0001c0001t0014g0281 | 2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-19-9429G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54868138 | ||||||
| chr18:54868210
|
A | G | 20 | a0001c0001t0001g0009a0001c0001t0001g0295a0001c0001t0001g0307others(17): Show | 22 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19-9357A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54868210 | ||||||
| chr18:54868257
|
A | G | 1 | a0001c0001t0033g0178 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-19-9310A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54868257 | ||||||
| chr18:54868425
|
C | T | 12 | a0001c0001t0001g0009a0001c0001t0001g0295a0001c0001t0001g0307others(9): Show | 13 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-9142C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54868425 | ||||||
| chr18:54868439
|
A | C | 1 | a0001c0001t0001g0247 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-19-9128A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54868439 | ||||||
| chr18:54868442
|
T | G | 1 | a0001c0001t0001g0077 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-19-9125T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54868442 | ||||||
| chr18:54868522
|
T | G | 1 | a0001c0001t0020g0091 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-19-9045T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54868522 | ||||||
| chr18:54868541
|
G | A | 1 | a0001c0001t0002g0261 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-19-9026G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54868541 | ||||||
| chr18:54868554
|
T | C | 95 | a0001c0001t0001g0031a0001c0001t0001g0054a0001c0001t0001g0062others(92): Show | 97 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.-19-9013T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54868554 | ||||||
| chr18:54868603
|
C | CGTT | 95 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0018others(92): Show | 97 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.-19-8945_-19-8943d others(5): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54868603 | |||||
| chr18:54868603
|
C | CGTTGTT | 126 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(123): Show | 128 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(125): Show |
intron_variant | MODIFIER | c.-19-8948_-19-8943d others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54868603 | |||||
| chr18:54868603
|
C | CGTTGTTG others(2): Show |
67 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0015others(64): Show | 71 | HG00099.hp1 HG00609.hp1 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.-19-8951_-19-8943d others(11): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54868603 | |||||
| chr18:54868603
|
C | CGTTGTTG others(5): Show |
6 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0059others(3): Show | 6 | HG02109.hp1 HG02602.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-8954_-19-8943d others(14): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54868603 | |||||
| chr18:54868603
|
C | CGTTGTTG others(8): Show |
1 | a0001c0001t0001g0088 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-19-8957_-19-8943d others(17): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54868603 | |||||
| chr18:54868641
|
G | T | 12 | a0001c0001t0001g0009a0001c0001t0001g0295a0001c0001t0001g0307others(9): Show | 13 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-8926G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54868641 | ||||||
| chr18:54868694
|
A | T | 308 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(305): Show | 317 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(314): Show |
intron_variant | MODIFIER | c.-19-8873A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54868694 | ||||||
| chr18:54868751
|
C | A | 3 | a0001c0001t0018g0134a0001c0001t0042g0109a0001c0001t0043g0112 | 3 | HG02965.hp1 HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-19-8816C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54868751 | ||||||
| chr18:54868776
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-19-8791G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54868776 | ||||||
| chr18:54868961
|
G | C | 1 | a0001c0001t0001g0175 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-19-8606G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54868961 | ||||||
| chr18:54869054
|
T | G | 1 | a0001c0001t0042g0109 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-19-8513T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54869054 | ||||||
| chr18:54869063
|
G | A | 1 | a0001c0001t0018g0134 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-19-8504G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54869063 | ||||||
| chr18:54869097
|
T | C | 1 | a0001c0001t0034g0310 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-19-8470T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54869097 | ||||||
| chr18:54869268
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-19-8299T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54869268 | ||||||
| chr18:54869268
|
T | G | 1 | a0001c0001t0006g0081 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-19-8299T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54869268 | ||||||
| chr18:54869378
|
C | A | 2 | a0001c0001t0008g0116a0001c0001t0033g0178 | 2 | HG02486.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-19-8189C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54869378 | ||||||
| chr18:54869471
|
G | A | 288 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(285): Show | 295 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(292): Show |
intron_variant | MODIFIER | c.-19-8096G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54869471 | ||||||
| chr18:54869493
|
A | G | 91 | a0001c0001t0001g0031a0001c0001t0001g0062a0001c0001t0001g0069others(88): Show | 93 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.-19-8074A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54869493 | ||||||
| chr18:54869669
|
A | C | 1 | a0001c0001t0004g0080 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-19-7898A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54869669 | ||||||
| chr18:54869715
|
A | G | 2 | a0001c0001t0014g0050a0001c0001t0014g0281 | 2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-19-7852A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54869715 | ||||||
| chr18:54869773
|
G | C | 1 | a0001c0001t0002g0035 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-19-7794G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54869773 | ||||||
| chr18:54869944
|
C | A | 1 | a0001c0001t0030g0104 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-19-7623C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54869944 | ||||||
| chr18:54869945
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-19-7622A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54869945 | ||||||
| chr18:54869962
|
G | A | 2 | a0001c0001t0004g0110a0001c0001t0029g0074 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-7605G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54869962 | ||||||
| chr18:54869999
|
A | G | 3 | a0001c0001t0001g0142a0001c0001t0002g0008a0001c0001t0002g0237 | 4 | HG01358.hp1 HG01978.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-7568A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54869999 | ||||||
| chr18:54870032
|
A | G | 288 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(285): Show | 295 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(292): Show |
intron_variant | MODIFIER | c.-19-7535A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54870032 | ||||||
| chr18:54870093
|
G | A | 88 | a0001c0001t0001g0031a0001c0001t0001g0062a0001c0001t0001g0069others(85): Show | 90 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.-19-7474G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54870093 | ||||||
| chr18:54870399
|
C | A | 91 | a0001c0001t0001g0031a0001c0001t0001g0062a0001c0001t0001g0069others(88): Show | 93 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.-19-7168C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54870399 | ||||||
| chr18:54870518
|
G | C | 12 | a0001c0001t0001g0009a0001c0001t0001g0295a0001c0001t0001g0307others(9): Show | 13 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-7049G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54870518 | ||||||
| chr18:54870544
|
A | T | 1 | a0001c0001t0004g0111 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-19-7023A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54870544 | ||||||
| chr18:54870578
|
G | A | 308 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(305): Show | 317 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(314): Show |
intron_variant | MODIFIER | c.-19-6989G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54870578 | ||||||
| chr18:54870840
|
C | T | 1 | a0001c0001t0004g0080 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-19-6727C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54870840 | ||||||
| chr18:54870847
|
G | A | 4 | a0001c0001t0012g0012a0001c0001t0012g0017a0001c0001t0012g0023others(1): Show | 4 | NA18941.hp1 NA19075.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-6720G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54870847 | ||||||
| chr18:54870895
|
A | T | 1 | a0001c0001t0008g0116 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-19-6672A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54870895 | ||||||
| chr18:54871003
|
A | G | 7 | a0001c0001t0005g0064a0001c0001t0005g0115a0001c0001t0005g0197others(4): Show | 7 | HG01168.hp1 HG01169.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-6564A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54871003 | ||||||
| chr18:54871152
|
A | T | 2 | a0001c0001t0004g0110a0001c0001t0029g0074 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-6415A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54871152 | ||||||
| chr18:54871233
|
C | T | 1 | a0001c0001t0004g0111 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-19-6334C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54871233 | ||||||
| chr18:54871632
|
C | T | 1 | a0001c0001t0010g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-19-5935C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54871632 | ||||||
| chr18:54871682
|
C | G | 1 | a0001c0001t0034g0310 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-19-5885C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54871682 | ||||||
| chr18:54871707
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-19-5860G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54871707 | ||||||
| chr18:54871724
|
C | G | 1 | a0001c0001t0014g0050 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-19-5843C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54871724 | ||||||
| chr18:54871849
|
C | CA | 89 | a0001c0001t0001g0031a0001c0001t0001g0062a0001c0001t0001g0069others(86): Show | 91 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.-19-5698dupA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54871849 | |||||
| chr18:54871849
|
C | CAA | 13 | a0001c0001t0001g0045a0001c0001t0001g0054a0001c0001t0001g0076others(10): Show | 13 | HG00642.hp2 HG02258.hp2 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-5699_-19-5698d others(4): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54871849 | |||||
| chr18:54871849
|
CA | C | 25 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028others(22): Show | 26 | HG00438.hp1 HG00735.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.-19-5698delA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54871849 | |||||
| chr18:54871849
|
CAAA | C | 11 | a0001c0001t0001g0009a0001c0001t0001g0295a0001c0001t0001g0307others(8): Show | 12 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-19-5700_-19-5698d others(5): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54871849 | |||||
| chr18:54871865
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-19-5702A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54871865 | ||||||
| chr18:54871903
|
G | A | 111 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0018others(108): Show | 112 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.-19-5664G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54871903 | ||||||
| chr18:54872087
|
A | T | 2 | a0001c0001t0002g0213a0001c0001t0045g0039 | 2 | HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-19-5480A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54872087 | ||||||
| chr18:54872100
|
G | C | 1 | a0001c0001t0002g0195 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-19-5467G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54872100 | ||||||
| chr18:54872114
|
A | G | 1 | a0001c0001t0043g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19-5453A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54872114 | ||||||
| chr18:54872374
|
C | T | 1 | a0001c0001t0002g0272 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-19-5193C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54872374 | ||||||
| chr18:54872397
|
G | A | 2 | a0001c0001t0008g0116a0001c0001t0033g0178 | 2 | HG02486.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-19-5170G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54872397 | ||||||
| chr18:54872438
|
C | A | 1 | a0001c0001t0010g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-19-5129C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54872438 | ||||||
| chr18:54872530
|
CAGG | C | 12 | a0001c0001t0001g0009a0001c0001t0001g0295a0001c0001t0001g0307others(9): Show | 13 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-5034_-19-5032d others(5): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54872530 | |||||
| chr18:54872565
|
C | T | 1 | a0001c0001t0002g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-19-5002C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54872565 | ||||||
| chr18:54872625
|
T | TA | 76 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0015others(73): Show | 80 | HG00099.hp1 HG00609.hp1 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.-19-4927dupA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54872625 | |||||
| chr18:54872625
|
TA | T | 113 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0018others(110): Show | 114 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.-19-4927delA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54872625 | |||||
| chr18:54873058
|
A | C | 1 | a0001c0001t0002g0199 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-19-4509A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54873058 | ||||||
| chr18:54873069
|
C | G | 1 | a0001c0001t0001g0088 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-19-4498C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54873069 | ||||||
| chr18:54873094
|
T | TCCTACTT others(309): Show |
2 | a0001c0001t0004g0110a0001c0001t0029g0074 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-4461_-19-4460i others(318): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873094 | |||||
| chr18:54873189
|
G | A | 209 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0018others(206): Show | 212 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(209): Show |
intron_variant | MODIFIER | c.-19-4378G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54873189 | ||||||
| chr18:54873496
|
T | C | 2 | a0001c0001t0004g0110a0001c0001t0029g0074 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-4071T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54873496 | ||||||
| chr18:54873510
|
C | T | 72 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0015others(69): Show | 76 | HG00099.hp1 HG00609.hp1 HG00673.hp2 others(73): Show |
intron_variant | MODIFIER | c.-19-4057C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54873510 | ||||||
| chr18:54873642
|
C | CAAAAAAA others(308): Show |
3 | a0001c0001t0001g0323a0001c0001t0018g0119a0003c0003t0031g0108 | 3 | HG00642.hp1 HG02145.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-19-3911_-19-3910i others(317): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873642 | |||||
| chr18:54873642
|
C | CAAAAAAA others(309): Show |
1 | a0001c0001t0040g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-19-3911_-19-3910i others(318): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873642 | |||||
| chr18:54873685
|
C | CTG | 62 | a0001c0001t0001g0018a0001c0001t0001g0062a0001c0001t0001g0070others(59): Show | 63 | HG00642.hp2 HG00735.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.-19-3839_-19-3838d others(4): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873685 | |||||
| chr18:54873685
|
C | CTGTG | 29 | a0001c0001t0001g0030a0001c0001t0001g0054a0001c0001t0001g0136others(26): Show | 29 | HG00639.hp1 HG01106.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.-19-3841_-19-3838d others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873685 | |||||
| chr18:54873685
|
C | CTGTGTG | 17 | a0001c0001t0001g0139a0001c0001t0001g0142a0001c0001t0001g0156others(14): Show | 17 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.-19-3843_-19-3838d others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873685 | |||||
| chr18:54873685
|
C | CTGTGTGT others(1): Show |
6 | a0001c0001t0001g0175a0001c0001t0001g0185a0001c0001t0001g0207others(3): Show | 6 | HG02129.hp1 HG04115.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19-3845_-19-3838d others(10): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873685 | |||||
| chr18:54873685
|
C | CTGTGTGT others(3): Show |
3 | a0001c0001t0001g0162a0001c0001t0002g0191a0001c0001t0033g0178 | 3 | HG00099.hp2 HG02486.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-19-3847_-19-3838d others(12): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873685 | |||||
| chr18:54873685
|
CTG | C | 35 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0031others(32): Show | 37 | HG01099.hp2 HG01243.hp2 HG01257.hp1 others(34): Show |
intron_variant | MODIFIER | c.-19-3839_-19-3838d others(4): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873685 | |||||
| chr18:54873685
|
CTGTG | C | 30 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028others(27): Show | 30 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.-19-3841_-19-3838d others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873685 | |||||
| chr18:54873685
|
CTGTGTG | C | 15 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0076others(12): Show | 15 | HG01175.hp2 HG02723.hp2 HG02818.hp1 others(12): Show |
intron_variant | MODIFIER | c.-19-3843_-19-3838d others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873685 | |||||
| chr18:54873685
|
CTGTGTGT others(1): Show |
C | 52 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(49): Show | 55 | HG00609.hp1 HG00673.hp2 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.-19-3845_-19-3838d others(10): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873685 | |||||
| chr18:54873685
|
CTGTGTGT others(3): Show |
C | 14 | a0001c0001t0001g0055a0001c0001t0003g0002a0001c0001t0003g0052others(11): Show | 15 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.-19-3847_-19-3838d others(12): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873685 | |||||
| chr18:54873685
|
CTGTGTGT others(5): Show |
C | 1 | a0002c0004t0007g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-19-3849_-19-3838d others(14): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873685 | |||||
| chr18:54873685
|
CTGTGTGT others(7): Show |
C | 2 | a0001c0001t0002g0234a0001c0001t0008g0004 | 3 | HG01433.hp2 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-19-3851_-19-3838d others(16): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873685 | |||||
| chr18:54873685
|
CTGTGTGT others(9): Show |
C | 3 | a0001c0001t0008g0060a0001c0001t0008g0066a0001c0001t0008g0082 | 3 | HG02622.hp1 HG02896.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-19-3853_-19-3838d others(18): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873685 | |||||
| chr18:54873685
|
CTGTGTGT others(13): Show |
C | 1 | a0001c0001t0002g0008 | 2 | HG03492.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-19-3857_-19-3838d others(22): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873685 | |||||
| chr18:54873730
|
A | T | 1 | a0001c0001t0004g0110 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-19-3837A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54873730 | ||||||
| chr18:54873752
|
TAGAC | T | 4 | a0001c0001t0001g0169a0001c0001t0004g0110a0001c0001t0028g0037others(1): Show | 4 | HG01934.hp1 HG01975.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-3811_-19-3808d others(6): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54873752 | |||||
| chr18:54873836
|
G | A | 287 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(284): Show | 294 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(291): Show |
intron_variant | MODIFIER | c.-19-3731G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54873836 | ||||||
| chr18:54873872
|
G | A | 7 | a0001c0001t0001g0015a0001c0001t0001g0125a0001c0001t0001g0126others(4): Show | 7 | NA18941.hp2 NA18948.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-3695G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54873872 | ||||||
| chr18:54873880
|
G | A | 287 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(284): Show | 294 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(291): Show |
intron_variant | MODIFIER | c.-19-3687G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54873880 | ||||||
| chr18:54873899
|
C | A | 7 | a0001c0001t0001g0015a0001c0001t0001g0125a0001c0001t0001g0126others(4): Show | 7 | NA18941.hp2 NA18948.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-3668C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54873899 | ||||||
| chr18:54874133
|
G | A | 2 | a0001c0001t0014g0050a0001c0001t0014g0281 | 2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-19-3434G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54874133 | ||||||
| chr18:54874174
|
A | G | 1 | a0001c0001t0043g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19-3393A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54874174 | ||||||
| chr18:54874268
|
A | C | 287 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(284): Show | 294 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(291): Show |
intron_variant | MODIFIER | c.-19-3299A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54874268 | ||||||
| chr18:54874519
|
A | G | 1 | a0001c0001t0018g0134 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-19-3048A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54874519 | ||||||
| chr18:54874540
|
G | A | 1 | a0001c0001t0043g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19-3027G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54874540 | ||||||
| chr18:54874547
|
T | C | 1 | a0001c0001t0018g0134 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-19-3020T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54874547 | ||||||
| chr18:54874557
|
T | C | 113 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0018others(110): Show | 114 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.-19-3010T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54874557 | ||||||
| chr18:54874562
|
T | TA | 11 | a0001c0001t0001g0009a0001c0001t0001g0295a0001c0001t0001g0307others(8): Show | 12 | HG01243.hp2 HG02055.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-19-2988dupA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54874562 | |||||
| chr18:54874562
|
TA | T | 204 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0018others(201): Show | 207 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(204): Show |
intron_variant | MODIFIER | c.-19-2988delA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54874562 | |||||
| chr18:54874562
|
TAA | T | 7 | a0001c0001t0001g0176a0001c0001t0001g0264a0001c0001t0001g0323others(4): Show | 7 | HG00642.hp1 HG01070.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-2989_-19-2988d others(4): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54874562 | |||||
| chr18:54874656
|
C | T | 1 | a0001c0001t0001g0174 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-19-2911C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54874656 | ||||||
| chr18:54874665
|
A | G | 8 | a0001c0001t0001g0009a0001c0001t0001g0295a0001c0001t0001g0307others(5): Show | 9 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19-2902A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54874665 | ||||||
| chr18:54874708
|
A | T | 3 | a0001c0001t0001g0020a0001c0001t0001g0122a0001c0001t0001g0124 | 3 | HG00609.hp1 HG02074.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.-19-2859A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54874708 | ||||||
| chr18:54874755
|
G | T | 307 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(304): Show | 316 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(313): Show |
intron_variant | MODIFIER | c.-19-2812G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54874755 | ||||||
| chr18:54874757
|
A | G | 287 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(284): Show | 294 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(291): Show |
intron_variant | MODIFIER | c.-19-2810A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54874757 | ||||||
| chr18:54874776
|
T | C | 7 | a0001c0001t0006g0011a0001c0001t0006g0081a0001c0001t0006g0083others(4): Show | 7 | HG01891.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-2791T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54874776 | ||||||
| chr18:54874930
|
T | C | 9 | a0001c0001t0001g0009a0001c0001t0001g0295a0001c0001t0001g0307others(6): Show | 10 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19-2637T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54874930 | ||||||
| chr18:54875081
|
C | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0232 | 2 | NA18954.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.-19-2486C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54875081 | ||||||
| chr18:54875194
|
C | T | 113 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0018others(110): Show | 114 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.-19-2373C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54875194 | ||||||
| chr18:54875341
|
T | A | 288 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(285): Show | 295 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(292): Show |
intron_variant | MODIFIER | c.-19-2226T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54875341 | ||||||
| chr18:54875539
|
AG | A | 208 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0018others(205): Show | 211 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(208): Show |
intron_variant | MODIFIER | c.-19-2026delG | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54875539 | |||||
| chr18:54875540
|
GGT | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0015others(76): Show | 83 | HG00099.hp1 HG00438.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.-19-2026_-19-2025d others(4): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54875540 | ||||||
| chr18:54875541
|
GT | G | 18 | a0001c0001t0001g0009a0001c0001t0001g0295a0001c0001t0001g0307others(15): Show | 20 | HG01243.hp2 HG01891.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.-19-2012delT | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54875541 | |||||
| chr18:54875542
|
T | A | 208 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0018others(205): Show | 211 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(208): Show |
intron_variant | MODIFIER | c.-19-2025T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54875542 | ||||||
| chr18:54875543
|
T | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0015others(76): Show | 83 | HG00099.hp1 HG00438.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.-19-2024T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54875543 | ||||||
| chr18:54875583
|
A | G | 1 | a0001c0001t0001g0323 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-19-1984A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54875583 | ||||||
| chr18:54875727
|
G | A | 6 | a0001c0001t0008g0004a0001c0001t0008g0014a0001c0001t0008g0060others(3): Show | 7 | HG01891.hp1 HG02622.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-1840G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54875727 | ||||||
| chr18:54875917
|
C | T | 1 | a0001c0001t0015g0016 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-19-1650C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54875917 | ||||||
| chr18:54875960
|
T | G | 4 | a0001c0001t0001g0323a0001c0001t0018g0119a0001c0001t0040g0194others(1): Show | 4 | HG00642.hp1 HG02145.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-1607T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54875960 | ||||||
| chr18:54876030
|
T | C | 2 | a0001c0001t0004g0110a0001c0001t0029g0074 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-1537T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54876030 | ||||||
| chr18:54876031
|
A | C | 1 | a0001c0001t0010g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-19-1536A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54876031 | ||||||
| chr18:54876053
|
G | A | 1 | a0001c0001t0020g0091 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-19-1514G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54876053 | ||||||
| chr18:54876086
|
T | C | 288 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(285): Show | 295 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(292): Show |
intron_variant | MODIFIER | c.-19-1481T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54876086 | ||||||
| chr18:54876098
|
G | A | 288 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(285): Show | 295 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(292): Show |
intron_variant | MODIFIER | c.-19-1469G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54876098 | ||||||
| chr18:54876130
|
G | A | 88 | a0001c0001t0001g0031a0001c0001t0001g0062a0001c0001t0001g0069others(85): Show | 90 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.-19-1437G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54876130 | ||||||
| chr18:54876387
|
G | C | 15 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(12): Show | 15 | HG00438.hp1 HG00735.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19-1180G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54876387 | ||||||
| chr18:54876419
|
GAGGTGGA others(22): Show |
G | 1 | a0001c0001t0001g0144 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-19-1146_-19-1118d others(31): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54876419 | |||||
| chr18:54876439
|
C | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0015others(70): Show | 77 | HG00099.hp1 HG00609.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.-19-1128C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54876439 | ||||||
| chr18:54876620
|
C | T | 1 | a0001c0001t0020g0091 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-19-947C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54876620 | ||||||
| chr18:54876655
|
T | C | 288 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(285): Show | 295 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(292): Show |
intron_variant | MODIFIER | c.-19-912T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54876655 | ||||||
| chr18:54876904
|
C | G | 18 | a0001c0001t0001g0009a0001c0001t0001g0295a0001c0001t0001g0307others(15): Show | 20 | HG01243.hp2 HG01891.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.-19-663C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54876904 | ||||||
| chr18:54876941
|
A | G | 2 | a0001c0001t0004g0110a0001c0001t0029g0074 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-626A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54876941 | ||||||
| chr18:54876985
|
C | A | 12 | a0001c0001t0001g0138a0001c0001t0001g0141a0001c0001t0001g0148others(9): Show | 12 | HG01109.hp2 HG01255.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-19-582C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54876985 | ||||||
| chr18:54877023
|
GT | G | 90 | a0001c0001t0001g0031a0001c0001t0001g0062a0001c0001t0001g0069others(87): Show | 92 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.-19-541delT | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 54877023 | |||||
| chr18:54877211
|
G | A | 1 | a0001c0001t0001g0006 | 2 | NA18970.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-19-356G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 1/5 | chr18 | 54877211 | ||||||
| chr18:54877776
|
C | T | 5 | a0001c0001t0010g0043a0001c0001t0018g0134a0001c0001t0030g0104others(2): Show | 5 | HG00738.hp2 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+38C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54877776 | ||||||
| chr18:54877782
|
A | G | 1 | a0001c0001t0010g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.153+44A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54877782 | ||||||
| chr18:54877841
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.153+103G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54877841 | ||||||
| chr18:54877983
|
A | T | 1 | a0001c0001t0024g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.153+245A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54877983 | ||||||
| chr18:54878017
|
A | G | 1 | a0001c0001t0002g0186 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.153+279A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54878017 | ||||||
| chr18:54878067
|
A | T | 1 | a0001c0001t0002g0218 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.153+329A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54878067 | ||||||
| chr18:54878074
|
T | C | 1 | a0001c0001t0043g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.153+336T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54878074 | ||||||
| chr18:54878218
|
C | T | 1 | a0001c0001t0019g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.153+480C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54878218 | ||||||
| chr18:54878580
|
T | A | 1 | a0001c0001t0002g0186 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.154-789T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54878580 | ||||||
| chr18:54878635
|
A | G | 1 | a0001c0001t0042g0109 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154-734A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54878635 | ||||||
| chr18:54878658
|
A | G | 96 | a0001c0001t0001g0031a0001c0001t0001g0062a0001c0001t0001g0069others(93): Show | 98 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.154-711A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54878658 | ||||||
| chr18:54878673
|
C | T | 3 | a0001c0001t0001g0101a0001c0001t0004g0118a0001c0001t0004g0317 | 3 | HG02647.hp1 HG02809.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.154-696C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54878673 | ||||||
| chr18:54878753
|
A | AT | 86 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0015others(83): Show | 90 | HG00099.hp1 HG00609.hp1 HG00673.hp2 others(87): Show |
intron_variant | MODIFIER | c.154-609dupT | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr18 | 54878753 | |||||
| chr18:54878760
|
T | A | 1 | a0001c0001t0002g0205 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.154-609T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54878760 | ||||||
| chr18:54878760
|
T | TA | 197 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0018others(194): Show | 200 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.154-602dupA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr18 | 54878760 | |||||
| chr18:54878781
|
A | C | 1 | a0001c0001t0001g0219 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.154-588A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54878781 | ||||||
| chr18:54879115
|
T | C | 71 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0069others(68): Show | 73 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.154-254T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54879115 | ||||||
| chr18:54879314
|
T | A | 1 | a0001c0001t0003g0002 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.154-55T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 2/5 | chr18 | 54879314 | ||||||
| chr18:54879482
|
T | C | 1 | a0001c0001t0041g0305 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.239+28T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54879482 | ||||||
| chr18:54879507
|
T | C | 1 | a0001c0001t0003g0002 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.239+53T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54879507 | ||||||
| chr18:54879639
|
G | C | 1 | a0001c0001t0008g0014 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.239+185G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54879639 | ||||||
| chr18:54879698
|
A | G | 1 | a0001c0001t0043g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.239+244A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54879698 | ||||||
| chr18:54879793
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.239+339G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54879793 | ||||||
| chr18:54879826
|
G | A | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0015others(189): Show | 198 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(195): Show |
intron_variant | MODIFIER | c.239+372G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54879826 | ||||||
| chr18:54879911
|
T | C | 24 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0072others(21): Show | 24 | HG00735.hp1 HG01168.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.239+457T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54879911 | ||||||
| chr18:54879949
|
C | T | 305 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(302): Show | 314 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(311): Show |
intron_variant | MODIFIER | c.239+495C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54879949 | ||||||
| chr18:54880059
|
C | A | 1 | a0001c0001t0001g0297 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.239+605C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54880059 | ||||||
| chr18:54880107
|
CA | C | 256 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(253): Show | 263 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(260): Show |
intron_variant | MODIFIER | c.239+654delA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54880107 | ||||||
| chr18:54880258
|
G | T | 2 | a0001c0001t0001g0113a0001c0001t0002g0114 | 2 | HG02818.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.239+804G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54880258 | ||||||
| chr18:54880310
|
A | G | 3 | a0001c0001t0010g0043a0001c0001t0010g0313a0001c0001t0040g0194 | 3 | HG03041.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.239+856A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54880310 | ||||||
| chr18:54880510
|
G | A | 7 | a0001c0001t0003g0003a0001c0001t0003g0032a0001c0001t0003g0034others(4): Show | 7 | HG01123.hp1 HG01256.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.239+1056G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54880510 | ||||||
| chr18:54880525
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0015others(74): Show | 81 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.239+1071G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54880525 | ||||||
| chr18:54880844
|
G | C | 309 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(306): Show | 318 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(315): Show |
intron_variant | MODIFIER | c.239+1390G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54880844 | ||||||
| chr18:54880878
|
A | T | 1 | a0001c0001t0008g0014 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.239+1424A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54880878 | ||||||
| chr18:54880892
|
G | A | 199 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(196): Show | 206 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(203): Show |
intron_variant | MODIFIER | c.239+1438G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54880892 | ||||||
| chr18:54881014
|
G | A | 76 | a0001c0001t0001g0031a0001c0001t0001g0113a0001c0001t0001g0247others(73): Show | 78 | HG00558.hp1 HG00621.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.239+1560G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54881014 | ||||||
| chr18:54881130
|
T | A | 107 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0018others(104): Show | 109 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.239+1676T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54881130 | ||||||
| chr18:54881169
|
C | T | 161 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0015others(158): Show | 167 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(164): Show |
intron_variant | MODIFIER | c.239+1715C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54881169 | ||||||
| chr18:54881315
|
G | A | 1 | a0001c0001t0001g0161 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.239+1861G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54881315 | ||||||
| chr18:54881333
|
A | G | 4 | a0001c0001t0001g0201a0001c0001t0001g0252a0001c0001t0001g0263others(1): Show | 4 | HG01081.hp1 HG01346.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.239+1879A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54881333 | ||||||
| chr18:54881339
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.239+1885G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54881339 | ||||||
| chr18:54881374
|
T | C | 306 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(303): Show | 315 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(312): Show |
intron_variant | MODIFIER | c.239+1920T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54881374 | ||||||
| chr18:54881395
|
C | T | 6 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(3): Show | 6 | HG00438.hp1 HG03831.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.239+1941C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54881395 | ||||||
| chr18:54881445
|
G | C | 1 | a0001c0001t0002g0258 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.239+1991G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54881445 | ||||||
| chr18:54881503
|
C | T | 2 | a0001c0001t0009g0089a0001c0001t0021g0090 | 2 | HG02055.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.239+2049C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54881503 | ||||||
| chr18:54881702
|
T | C | 306 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(303): Show | 315 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(312): Show |
intron_variant | MODIFIER | c.239+2248T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54881702 | ||||||
| chr18:54881720
|
G | A | 3 | a0001c0001t0008g0014a0001c0001t0014g0050a0001c0001t0014g0281 | 3 | HG03471.hp1 HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.239+2266G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54881720 | ||||||
| chr18:54881764
|
A | C | 100 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0018others(97): Show | 101 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.239+2310A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54881764 | ||||||
| chr18:54881793
|
G | A | 1 | a0001c0001t0002g0199 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.239+2339G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54881793 | ||||||
| chr18:54882033
|
G | T | 2 | a0001c0001t0009g0089a0001c0001t0021g0090 | 2 | HG02055.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.240-2300G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54882033 | ||||||
| chr18:54882165
|
G | A | 305 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(302): Show | 314 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(311): Show |
intron_variant | MODIFIER | c.240-2168G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54882165 | ||||||
| chr18:54882368
|
G | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0015others(70): Show | 77 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.240-1965G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54882368 | ||||||
| chr18:54882501
|
G | A | 2 | a0001c0001t0014g0050a0001c0001t0014g0281 | 2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.240-1832G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54882501 | ||||||
| chr18:54882518
|
T | C | 1 | a0001c0001t0042g0109 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.240-1815T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54882518 | ||||||
| chr18:54882541
|
G | A | 1 | a0001c0001t0010g0190 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.240-1792G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54882541 | ||||||
| chr18:54882597
|
T | G | 1 | a0001c0001t0030g0104 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.240-1736T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54882597 | ||||||
| chr18:54882690
|
G | C | 76 | a0001c0001t0001g0031a0001c0001t0001g0113a0001c0001t0001g0247others(73): Show | 78 | HG00558.hp1 HG00621.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.240-1643G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54882690 | ||||||
| chr18:54882830
|
C | T | 86 | a0001c0001t0001g0031a0001c0001t0001g0113a0001c0001t0001g0247others(83): Show | 88 | HG00558.hp1 HG00621.hp1 HG00642.hp2 others(85): Show |
intron_variant | MODIFIER | c.240-1503C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54882830 | ||||||
| chr18:54882920
|
A | T | 1 | a0001c0001t0004g0067 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.240-1413A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54882920 | ||||||
| chr18:54883055
|
A | G | 1 | a0001c0001t0006g0081 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.240-1278A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54883055 | ||||||
| chr18:54883370
|
T | A | 3 | a0001c0001t0010g0190a0001c0001t0014g0050a0001c0001t0014g0281 | 3 | HG03195.hp1 HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.240-963T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54883370 | ||||||
| chr18:54883387
|
A | G | 163 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0015others(160): Show | 169 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(166): Show |
intron_variant | MODIFIER | c.240-946A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54883387 | ||||||
| chr18:54883390
|
G | A | 1 | a0001c0001t0002g0206 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.240-943G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54883390 | ||||||
| chr18:54883646
|
G | A | 1 | a0001c0001t0034g0310 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.240-687G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54883646 | ||||||
| chr18:54883839
|
A | G | 1 | a0001c0001t0003g0002 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.240-494A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54883839 | ||||||
| chr18:54884093
|
CTG | C | 22 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0072others(19): Show | 22 | HG00735.hp1 HG01168.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.240-234_240-233del others(2): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr18 | 54884093 | |||||
| chr18:54884094
|
T | A | 2 | a0001c0001t0014g0050a0001c0001t0014g0281 | 2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.240-239T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54884094 | ||||||
| chr18:54884139
|
T | TA | 14 | a0001c0001t0001g0054a0001c0001t0001g0176a0001c0001t0001g0270others(11): Show | 14 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.240-183dupA | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr18 | 54884139 | |||||
| chr18:54884224
|
T | C | 2 | a0001c0001t0002g0248a0001c0001t0002g0280 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.240-109T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54884224 | ||||||
| chr18:54884310
|
T | C | 2 | a0001c0001t0014g0050a0001c0001t0014g0281 | 2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.240-23T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 3/5 | chr18 | 54884310 | ||||||
| chr18:54884466
|
C | T | 1 | a0001c0001t0042g0109 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.343+30C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54884466 | ||||||
| chr18:54884485
|
C | T | 97 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0018others(94): Show | 98 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.343+49C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54884485 | ||||||
| chr18:54884575
|
TGTGTCAC others(1): Show |
T | 3 | a0001c0001t0010g0190a0001c0001t0014g0050a0001c0001t0014g0281 | 3 | HG03195.hp1 HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.343+140_343+147del others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54884575 | ||||||
| chr18:54884596
|
G | A | 2 | a0001c0001t0005g0289a0001c0001t0005g0290 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.343+160G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54884596 | ||||||
| chr18:54884610
|
C | A | 1 | a0001c0001t0042g0109 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.343+174C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54884610 | ||||||
| chr18:54884621
|
G | C | 85 | a0001c0001t0001g0031a0001c0001t0001g0113a0001c0001t0001g0247others(82): Show | 87 | HG00558.hp1 HG00621.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.343+185G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54884621 | ||||||
| chr18:54884678
|
T | C | 2 | a0001c0001t0014g0050a0001c0001t0014g0281 | 2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.343+242T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54884678 | ||||||
| chr18:54884800
|
G | A | 311 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(308): Show | 320 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(317): Show |
intron_variant | MODIFIER | c.343+364G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54884800 | ||||||
| chr18:54884905
|
G | A | 1 | a0001c0001t0007g0296 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.343+469G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54884905 | ||||||
| chr18:54884936
|
T | C | 1 | a0001c0001t0002g0243 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.343+500T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54884936 | ||||||
| chr18:54884953
|
G | A | 1 | a0001c0001t0010g0190 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.343+517G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54884953 | ||||||
| chr18:54885623
|
CATCACTC others(3): Show |
C | 8 | a0001c0001t0001g0009a0001c0001t0001g0295a0001c0001t0001g0307others(5): Show | 9 | HG01243.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.343+1191_343+1200d others(12): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr18 | 54885623 | |||||
| chr18:54885630
|
C | G | 298 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(295): Show | 306 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(303): Show |
intron_variant | MODIFIER | c.343+1194C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54885630 | ||||||
| chr18:54885641
|
C | T | 1 | a0001c0001t0040g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.343+1205C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54885641 | ||||||
| chr18:54885648
|
C | T | 5 | a0001c0001t0010g0043a0001c0001t0010g0313a0001c0001t0018g0119others(2): Show | 5 | HG02965.hp1 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.343+1212C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54885648 | ||||||
| chr18:54885655
|
G | A | 9 | a0001c0001t0004g0110a0001c0001t0008g0004a0001c0001t0008g0014others(6): Show | 10 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.343+1219G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54885655 | ||||||
| chr18:54885671
|
T | A | 1 | a0001c0001t0003g0034 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.343+1235T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54885671 | ||||||
| chr18:54885815
|
G | T | 306 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(303): Show | 315 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(312): Show |
intron_variant | MODIFIER | c.343+1379G>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54885815 | ||||||
| chr18:54885864
|
T | C | 2 | a0001c0001t0001g0015a0001c0001t0023g0140 | 2 | NA18963.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.343+1428T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54885864 | ||||||
| chr18:54885973
|
A | G | 1 | a0001c0001t0004g0321 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.343+1537A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54885973 | ||||||
| chr18:54886121
|
C | A | 9 | a0001c0001t0004g0110a0001c0001t0008g0004a0001c0001t0008g0014others(6): Show | 10 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.343+1685C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54886121 | ||||||
| chr18:54886121
|
C | G | 1 | a0001c0001t0019g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.343+1685C>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54886121 | ||||||
| chr18:54886241
|
T | A | 2 | a0001c0001t0014g0050a0001c0001t0014g0281 | 2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.344-1754T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54886241 | ||||||
| chr18:54886313
|
G | A | 84 | a0001c0001t0001g0031a0001c0001t0001g0247a0001c0001t0002g0007others(81): Show | 86 | HG00558.hp1 HG00621.hp1 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.344-1682G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54886313 | ||||||
| chr18:54886397
|
A | T | 39 | a0001c0001t0001g0009a0001c0001t0001g0057a0001c0001t0001g0065others(36): Show | 40 | HG00735.hp1 HG00738.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.344-1598A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54886397 | ||||||
| chr18:54886416
|
A | G | 1 | a0001c0001t0020g0091 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.344-1579A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54886416 | ||||||
| chr18:54886423
|
G | A | 297 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(294): Show | 305 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(302): Show |
intron_variant | MODIFIER | c.344-1572G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54886423 | ||||||
| chr18:54886513
|
A | C | 1 | a0001c0001t0010g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.344-1482A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54886513 | ||||||
| chr18:54886640
|
C | A | 1 | a0001c0001t0042g0109 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.344-1355C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54886640 | ||||||
| chr18:54886697
|
T | C | 2 | a0001c0001t0014g0050a0001c0001t0014g0281 | 2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.344-1298T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54886697 | ||||||
| chr18:54886798
|
A | C | 4 | a0001c0001t0001g0188a0001c0001t0001g0207a0001c0001t0001g0230others(1): Show | 4 | NA18961.hp2 NA19004.hp1 NA19075.hp2 others(1): Show |
intron_variant | MODIFIER | c.344-1197A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54886798 | ||||||
| chr18:54886830
|
A | G | 309 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(306): Show | 318 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(315): Show |
intron_variant | MODIFIER | c.344-1165A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54886830 | ||||||
| chr18:54886929
|
A | G | 2 | a0001c0001t0008g0060a0001c0001t0008g0066 | 2 | HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.344-1066A>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54886929 | ||||||
| chr18:54887021
|
T | TCCTC | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0015others(70): Show | 77 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.344-954_344-951dup others(4): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr18 | 54887021 | |||||
| chr18:54887021
|
T | TCCTCCCT others(1): Show |
3 | a0001c0001t0001g0045a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | HG02602.hp2 HG03704.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.344-958_344-951dup others(8): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr18 | 54887021 | |||||
| chr18:54887021
|
TCCTC | T | 10 | a0001c0001t0001g0156a0001c0001t0001g0160a0001c0001t0004g0110others(7): Show | 11 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.344-954_344-951del others(4): Show |
RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr18 | 54887021 | |||||
| chr18:54887050
|
A | C | 324 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(321): Show | 333 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(330): Show |
intron_variant | MODIFIER | c.344-945A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54887050 | ||||||
| chr18:54887094
|
C | T | 1 | a0001c0001t0043g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.344-901C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54887094 | ||||||
| chr18:54887110
|
G | C | 1 | a0001c0001t0043g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.344-885G>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54887110 | ||||||
| chr18:54887327
|
A | C | 1 | a0001c0001t0023g0140 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.344-668A>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54887327 | ||||||
| chr18:54887425
|
G | A | 311 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(308): Show | 320 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(317): Show |
intron_variant | MODIFIER | c.344-570G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54887425 | ||||||
| chr18:54887429
|
T | A | 1 | a0001c0001t0010g0190 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.344-566T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54887429 | ||||||
| chr18:54887463
|
G | A | 1 | a0001c0001t0024g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.344-532G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54887463 | ||||||
| chr18:54887535
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.344-460G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54887535 | ||||||
| chr18:54887605
|
G | A | 306 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(303): Show | 315 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(312): Show |
intron_variant | MODIFIER | c.344-390G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54887605 | ||||||
| chr18:54887661
|
C | T | 1 | a0001c0001t0008g0014 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.344-334C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54887661 | ||||||
| chr18:54887704
|
T | G | 1 | a0003c0003t0031g0108 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.344-291T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54887704 | ||||||
| chr18:54887866
|
T | A | 1 | a0001c0001t0025g0318 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.344-129T>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 4/5 | chr18 | 54887866 | ||||||
| chr18:54888149
|
C | A | 1 | a0003c0003t0031g0108 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.467+31C>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 5/5 | chr18 | 54888149 | ||||||
| chr18:54888167
|
G | A | 306 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(303): Show | 315 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(312): Show |
intron_variant | MODIFIER | c.467+49G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 5/5 | chr18 | 54888167 | ||||||
| chr18:54888261
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.467+143T>C | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 5/5 | chr18 | 54888261 | ||||||
| chr18:54888354
|
T | G | 2 | a0001c0001t0002g0213a0001c0001t0045g0039 | 2 | HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.467+236T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 5/5 | chr18 | 54888354 | ||||||
| chr18:54888373
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.467+255G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 5/5 | chr18 | 54888373 | ||||||
| chr18:54888431
|
G | A | 4 | a0001c0001t0005g0048a0001c0001t0005g0049a0001c0001t0005g0051others(1): Show | 4 | HG00738.hp1 HG01081.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.467+313G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 5/5 | chr18 | 54888431 | ||||||
| chr18:54888584
|
G | A | 2 | a0001c0001t0014g0050a0001c0001t0014g0281 | 2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.467+466G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 5/5 | chr18 | 54888584 | ||||||
| chr18:54888663
|
C | T | 1 | a0001c0001t0002g0246 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.467+545C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 5/5 | chr18 | 54888663 | ||||||
| chr18:54888751
|
G | A | 1 | a0001c0001t0010g0190 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.468-473G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 5/5 | chr18 | 54888751 | ||||||
| chr18:54888972
|
T | G | 2 | a0001c0001t0014g0050a0001c0001t0014g0281 | 2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.468-252T>G | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 5/5 | chr18 | 54888972 | ||||||
| chr18:54889017
|
A | T | 1 | a0001c0001t0001g0161 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.468-207A>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 5/5 | chr18 | 54889017 | ||||||
| chr18:54889135
|
G | A | 1 | a0001c0001t0033g0178 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.468-89G>A | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 5/5 | chr18 | 54889135 | ||||||
| chr18:54889174
|
C | T | 1 | a0001c0001t0010g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.468-50C>T | RAB27B | ENSG00000041353.10 | transcript | ENST00000262094.10 | protein_coding | 5/5 | chr18 | 54889174 |