Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 57148 |
|---|---|
| ensemblid | ENSG00000170471.15 |
| hgncid | 29221 |
| symbol | RALGAPB |
| name | Ral GTPase activating protein non-catalytic subunit beta |
| refseq_nuc | NM_020336.4 |
| refseq_prot | NP_065069.1 |
| ensembl_nuc | ENST00000262879.11 |
| ensembl_prot | ENSP00000262879.6 |
| mane_status | MANE Select |
| chr | chr20 |
| start | 38472843 |
| end | 38578858 |
| strand | + |
| ver | v1.2 |
| region | chr20:38472843-38578858 |
| region5000 | chr20:38467843-38583858 |
| regionname0 | RALGAPB_chr20_38472843_38578858 |
| regionname5000 | RALGAPB_chr20_38467843_38583858 |
| 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 | 1494 | 210 | 80 | 40 | 61 | 6 | 21 | 51 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0002 | 0/0 | 1494 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0003 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0004 | 0/0 | 1494 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0005 | 0/0 | 1494 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| 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 | 4485 | 175 | 55 | 35 | 56 | 6 | 21 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| c0002 | 0/0 | 4485 | 15 | 12 | 3 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| c0003 | 0/0 | 4485 | 14 | 13 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| c0004 | 0/0 | 4485 | 3 | 3 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| c0005 | 0/0 | 4485 | 2 | 0 | 0 | 2 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| c0006 | 0/0 | 4485 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| c0007 | 0/0 | 4485 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| c0008 | 0/0 | 4485 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| c0009 | 0/0 | 4485 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| c0010 | 0/0 | 4485 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| c0011 | 0/0 | 4485 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| c0012 | 0/0 | 4485 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| 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 | 4151 | 85 | 13 | 14 | 44 | 1 | 12 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| t0002 | 0/0 | 4149 | 40 | 15 | 9 | 8 | 3 | 5 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| t0003 | 0/0 | 4153 | 28 | 7 | 6 | 9 | 2 | 4 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| t0004 | 0/0 | 4143 | 11 | 10 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| t0005 | 0/0 | 4154 | 9 | 9 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| t0006 | 0/0 | 4147 | 7 | 7 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| t0007 | 0/0 | 4147 | 4 | 1 | 3 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| t0008 | 0/0 | 4149 | 3 | 3 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| t0009 | 0/0 | 4157 | 3 | 3 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| t0010 | 0/0 | 4152 | 3 | 3 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| t0011 | 0/0 | 4159 | 2 | 1 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| t0012 | 0/0 | 4156 | 2 | 1 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| t0013 | 1/0 | 4149 | 1 | 0 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| t0014 | 0/0 | 4151 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| t0015 | 0/0 | 4153 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| t0016 | 0/0 | 4151 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| t0017 | 0/0 | 4149 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| t0018 | 0/0 | 4149 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| t0019 | 0/0 | 4149 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| t0020 | 0/0 | 4155 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| t0021 | 0/0 | 4159 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| t0022 | 0/0 | 4157 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| t0023 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| t0024 | 0/0 | 4155 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| t0025 | 0/0 | 4151 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| t0026 | 0/0 | 4151 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| t0027 | 0/0 | 4155 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| t0028 | 0/0 | 4151 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| t0029 | 0/0 | 4155 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| t0030 | 0/0 | 4153 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| t0031 | 0/0 | 4149 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0046 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0157 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| 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 | 4485 | 175 | 55 | 35 | 56 | 6 | 21 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0002 | 0/0 | 4485 | 15 | 12 | 3 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0003 | 0/0 | 4485 | 14 | 13 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0005 | 0/0 | 4485 | 2 | 0 | 0 | 2 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0007 | 0/0 | 4485 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0008 | 0/0 | 4485 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0009 | 0/0 | 4485 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0012 | 0/0 | 4485 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0002c0004 | 0/0 | 4485 | 3 | 3 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0003c0006 | 0/0 | 4485 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0004c0010 | 0/0 | 4485 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0005c0011 | 0/0 | 4485 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 8635 | 79 | 13 | 13 | 39 | 1 | 12 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0001t0002 | 0/0 | 8633 | 27 | 4 | 8 | 8 | 3 | 4 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0001t0003 | 0/0 | 8637 | 26 | 6 | 6 | 8 | 2 | 4 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0001t0004 | 0/0 | 8627 | 11 | 10 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0001t0006 | 0/0 | 8631 | 7 | 7 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0001t0007 | 0/0 | 8631 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0001t0008 | 0/0 | 8633 | 3 | 3 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0001t0009 | 0/0 | 8641 | 3 | 3 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0001t0011 | 0/0 | 8643 | 2 | 1 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0001t0013 | 1/0 | 8633 | 1 | 0 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0001t0014 | 0/0 | 8635 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0001t0015 | 0/0 | 8637 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0001t0016 | 0/0 | 8635 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0001t0017 | 0/0 | 8633 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0001t0018 | 0/0 | 8633 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0001t0019 | 0/0 | 8633 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0001t0020 | 0/0 | 8639 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0001t0021 | 0/0 | 8643 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0001t0022 | 0/0 | 8641 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0001t0023 | 0/0 | 8627 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0001t0024 | 0/0 | 8639 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0001t0025 | 0/0 | 8635 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0001t0026 | 0/0 | 8635 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0001t0027 | 0/0 | 8639 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0001t0028 | 0/0 | 8635 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0002t0002 | 0/0 | 8633 | 12 | 11 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0002t0007 | 0/0 | 8631 | 3 | 1 | 2 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0003t0005 | 0/0 | 8638 | 9 | 9 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0003t0010 | 0/0 | 8636 | 3 | 3 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0003t0012 | 0/0 | 8640 | 2 | 1 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0005t0001 | 0/0 | 8635 | 2 | 0 | 0 | 2 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0007t0003 | 0/0 | 8637 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0008t0001 | 0/0 | 8635 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0009t0001 | 0/0 | 8635 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0001c0012t0001 | 0/0 | 8635 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0002c0004t0029 | 0/0 | 8639 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0002c0004t0030 | 0/0 | 8637 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0002c0004t0031 | 0/0 | 8633 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0003c0006t0003 | 0/0 | 8637 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0004c0010t0001 | 0/0 | 8635 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| a0005c0011t0002 | 0/0 | 8633 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | copy fasta | chr20 | 38467843 | 38583858 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0046 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0004g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0006g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0007g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0008g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0008g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0008g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0009g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0009g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0009g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0011g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0011g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0013g0157 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0014g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0015g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0016g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0017g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0018g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0019g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0020g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0021g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0022g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0023g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0024g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0025g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0026g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0027g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0001t0028g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0002t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0002t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0002t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0002t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0002t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0002t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0002t0007g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0002t0007g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0003t0005g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0003t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0003t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0003t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0003t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0003t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0003t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0003t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0003t0010g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0003t0010g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0003t0010g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0003t0012g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0005t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0005t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0007t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0008t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0009t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0001c0012t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0002c0004t0029g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0002c0004t0030g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0002c0004t0031g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0003c0006t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0004c0010t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| a0005c0011t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0059 | EUR | FIN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0143 | EUR | FIN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG00642 | hp2 | a0001 | c0002 | t0007 | g0004 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0152 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0078 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG00738 | hp2 | a0001 | c0001 | t0007 | g0163 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0035 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01081 | hp1 | a0001 | c0001 | t0015 | g0050 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01106 | hp1 | a0001 | c0008 | t0001 | g0049 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01106 | hp2 | a0001 | c0001 | t0028 | g0066 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01109 | hp1 | a0001 | c0003 | t0012 | g0006 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01243 | hp1 | a0001 | c0001 | t0025 | g0097 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0133 | AMR | PUR | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0058 | AMR | CLM | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | CLM | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | CLM | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01361 | hp1 | a0001 | c0001 | t0011 | g0013 | AMR | CLM | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0092 | AMR | CLM | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01433 | hp2 | a0001 | c0002 | t0007 | g0004 | AMR | CLM | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0145 | EUR | IBS | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0036 | EUR | IBS | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0149 | EUR | IBS | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01884 | hp1 | a0001 | c0001 | t0023 | g0026 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0030 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | PEL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0061 | AMR | PEL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG01993 | hp2 | a0001 | c0001 | t0018 | g0151 | AMR | PEL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | PEL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02027 | hp1 | a0001 | c0009 | t0001 | g0088 | EAS | KHV | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | KHV | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02055 | hp1 | a0001 | c0001 | t0021 | g0023 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | KHV | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02145 | hp1 | a0001 | c0001 | t0011 | g0014 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0128 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0122 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02258 | hp2 | a0002 | c0004 | t0029 | g0008 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02293 | hp1 | a0001 | c0001 | t0016 | g0043 | AMR | PEL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | PEL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02451 | hp1 | a0001 | c0003 | t0005 | g0005 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02451 | hp2 | a0001 | c0001 | t0017 | g0175 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0021 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0068 | SAS | PJL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02622 | hp1 | a0001 | c0003 | t0010 | g0201 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02622 | hp2 | a0001 | c0001 | t0027 | g0121 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0126 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0002 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0129 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02723 | hp1 | a0001 | c0003 | t0010 | g0202 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0104 | SAS | PJL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0130 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0197 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02886 | hp1 | a0001 | c0001 | t0020 | g0039 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0108 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0032 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02896 | hp1 | a0001 | c0001 | t0008 | g0171 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02896 | hp2 | a0001 | c0003 | t0005 | g0210 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0110 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02897 | hp2 | a0001 | c0001 | t0008 | g0172 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02922 | hp1 | a0001 | c0001 | t0009 | g0011 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02922 | hp2 | a0001 | c0003 | t0005 | g0206 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0109 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0127 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02970 | hp1 | a0001 | c0001 | t0024 | g0015 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02970 | hp2 | a0001 | c0003 | t0005 | g0204 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0124 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | GWD | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0179 | AFR | MSL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | MSL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0031 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03130 | hp2 | a0001 | c0001 | t0009 | g0012 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0027 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03139 | hp2 | a0001 | c0003 | t0005 | g0207 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03195 | hp1 | a0001 | c0003 | t0005 | g0208 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0123 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | MSL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0107 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03516 | hp2 | a0001 | c0001 | t0009 | g0010 | AFR | ESN | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0016 | AFR | MSL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03579 | hp2 | a0001 | c0003 | t0012 | g0006 | AFR | MSL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0079 | SAS | PJL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03669 | hp2 | a0005 | c0011 | t0002 | g0160 | SAS | PJL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03688 | hp2 | a0001 | c0001 | t0026 | g0113 | SAS | STU | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0147 | SAS | BEB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0082 | SAS | BEB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0155 | SAS | BEB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | BEB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0168 | SAS | STU | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | STU | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0132 | AFR | YRI | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18522 | hp2 | a0001 | c0003 | t0005 | g0005 | AFR | YRI | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | YRI | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0173 | AFR | YRI | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18954 | hp1 | a0001 | c0001 | t0014 | g0087 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18979 | hp1 | a0004 | c0010 | t0001 | g0111 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18999 | hp1 | a0001 | c0012 | t0001 | g0075 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19001 | hp1 | a0001 | c0007 | t0003 | g0067 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19030 | hp1 | a0001 | c0001 | t0019 | g0194 | AFR | LWK | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19030 | hp2 | a0001 | c0003 | t0010 | g0209 | AFR | LWK | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0125 | AFR | LWK | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19043 | hp2 | a0002 | c0004 | t0031 | g0009 | AFR | LWK | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19059 | hp1 | a0001 | c0005 | t0001 | g0118 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19059 | hp2 | a0001 | c0005 | t0001 | g0117 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0131 | AFR | YRI | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA19240 | hp2 | a0001 | c0003 | t0005 | g0205 | AFR | YRI | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02109 | hp1 | a0001 | c0002 | t0007 | g0134 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02109 | hp2 | a0001 | c0001 | t0022 | g0022 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02486 | hp1 | a0002 | c0004 | t0030 | g0007 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02486 | hp2 | a0003 | c0006 | t0003 | g0033 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | ACB | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0002 | AFR | MSL | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | USA | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | USA | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0029 | AFR | USA | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | USA | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0182 | AFR | LWK | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| NA21309 | hp2 | a0001 | c0003 | t0005 | g0203 | AFR | LWK | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0046 | REF | REF | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0013 | g0157 | REF | REF | RALGAPB_chr20_38467843_38583858 | RALGAPB | chr20 | 38467843 | 38583858 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:38521596
|
C | G | 1 | a0005 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.1517C>G | p.Pro506Arg | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/30 | 1774/8633 | 1517/4485 | 506/1494 | chr20 | 38521596 | ||
| chr20:38532803
|
C | T | 1 | a0002 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
missense_variant | MODERATE | c.2189C>T | p.Thr730Met | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/30 | 2446/8633 | 2189/4485 | 730/1494 | chr20 | 38532803 | ||
| chr20:38539810
|
G | A | 1 | a0005 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.2414G>A | p.Arg805Gln | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 17/30 | 2671/8633 | 2414/4485 | 805/1494 | chr20 | 38539810 | ||
| chr20:38551125
|
T | G | 1 | a0003 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.3064T>G | p.Ser1022Ala | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/30 | 3321/8633 | 3064/4485 | 1022/1494 | chr20 | 38551125 | ||
| chr20:38574894
|
G | A | 1 | a0004 | 1 | NA18979.hp1 | missense_variant | MODERATE | c.4412G>A | p.Arg1471Gln | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 4669/8633 | 4412/4485 | 1471/1494 | chr20 | 38574894 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:38517867
|
A | G | 1 | a0002c0004 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
synonymous_variant | LOW | c.1284A>G | p.Glu428Glu | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/30 | 1541/8633 | 1284/4485 | 428/1494 | chr20 | 38517867 | ||
| chr20:38517921
|
C | G | 1 | a0001c0012 | 1 | NA18999.hp1 | synonymous_variant | LOW | c.1338C>G | p.Leu446Leu | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/30 | 1595/8633 | 1338/4485 | 446/1494 | chr20 | 38517921 | ||
| chr20:38539826
|
G | T | 1 | a0001c0003 | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
synonymous_variant | LOW | c.2430G>T | p.Val810Val | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 17/30 | 2687/8633 | 2430/4485 | 810/1494 | chr20 | 38539826 | ||
| chr20:38539877
|
G | A | 1 | a0001c0005 | 2 | NA19059.hp1 NA19059.hp2 |
synonymous_variant | LOW | c.2481G>A | p.Arg827Arg | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 17/30 | 2738/8633 | 2481/4485 | 827/1494 | chr20 | 38539877 | ||
| chr20:38548780
|
A | G | 1 | a0001c0002 | 15 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(12): Show |
synonymous_variant | LOW | c.2994A>G | p.Ala998Ala | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/30 | 3251/8633 | 2994/4485 | 998/1494 | chr20 | 38548780 | ||
| chr20:38567130
|
T | C | 1 | a0001c0007 | 1 | NA19001.hp1 | synonymous_variant | LOW | c.3852T>C | p.Asp1284Asp | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/30 | 4109/8633 | 3852/4485 | 1284/1494 | chr20 | 38567130 | ||
| chr20:38570800
|
G | A | 1 | a0001c0008 | 1 | HG01106.hp1 | synonymous_variant | LOW | c.4095G>A | p.Glu1365Glu | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/30 | 4352/8633 | 4095/4485 | 1365/1494 | chr20 | 38570800 | ||
| chr20:38574841
|
T | C | 1 | a0001c0009 | 1 | HG02027.hp1 | synonymous_variant | LOW | c.4359T>C | p.Ser1453Ser | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 4616/8633 | 4359/4485 | 1453/1494 | chr20 | 38574841 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:38575064
|
C | T | 3 | a0002c0004t0029a0002c0004t0030a0002c0004t0031 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*97C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 97 | chr20 | 38575064 | |||||
| chr20:38575170
|
C | T | 40 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(37): Show | 215 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*203C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 203 | chr20 | 38575170 | |||||
| chr20:38575177
|
G | T | 1 | a0001c0001t0028 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*210G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 210 | chr20 | 38575177 | |||||
| chr20:38575389
|
A | G | 1 | a0001c0001t0027 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*422A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 422 | chr20 | 38575389 | |||||
| chr20:38575527
|
TAAG | T | 3 | a0001c0003t0005a0001c0003t0010a0001c0003t0012 | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*564_*566delAAG | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 564 | INFO_REALIGN_3_PRIME | chr20 | 38575527 | ||||
| chr20:38575800
|
A | G | 1 | a0001c0001t0026 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*833A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 833 | chr20 | 38575800 | |||||
| chr20:38576096
|
T | G | 1 | a0001c0001t0014 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1129T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 1129 | chr20 | 38576096 | |||||
| chr20:38576188
|
T | C | 1 | a0001c0001t0015 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1221T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 1221 | chr20 | 38576188 | |||||
| chr20:38576199
|
C | T | 1 | a0001c0001t0025 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1232C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 1232 | chr20 | 38576199 | |||||
| chr20:38576864
|
C | T | 8 | a0001c0001t0004a0001c0001t0009a0001c0001t0011others(5): Show | 32 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1897C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 1897 | chr20 | 38576864 | |||||
| chr20:38576919
|
T | G | 1 | a0001c0001t0023 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1952T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 1952 | chr20 | 38576919 | |||||
| chr20:38577017
|
T | C | 1 | a0001c0001t0016 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2050T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2050 | chr20 | 38577017 | |||||
| chr20:38577185
|
C | T | 2 | a0001c0001t0021a0001c0001t0022 | 2 | HG02055.hp1 HG02109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2218C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2218 | chr20 | 38577185 | |||||
| chr20:38577249
|
T | C | 10 | a0001c0001t0004a0001c0001t0009a0001c0001t0011others(7): Show | 34 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2282T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2282 | chr20 | 38577249 | |||||
| chr20:38577391
|
T | G | 2 | a0001c0001t0021a0001c0001t0022 | 2 | HG02055.hp1 HG02109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2424T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2424 | chr20 | 38577391 | |||||
| chr20:38577452
|
G | T | 1 | a0001c0001t0020 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2485G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2485 | chr20 | 38577452 | |||||
| chr20:38577484
|
G | A | 1 | a0001c0001t0017 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2517G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2517 | chr20 | 38577484 | |||||
| chr20:38577513
|
C | T | 1 | a0001c0001t0019 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2546C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2546 | chr20 | 38577513 | |||||
| chr20:38577698
|
G | GAC | 12 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(9): Show | 97 | HG00558.hp1 HG00558.hp2 HG00639.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*2764_*2765dupAC | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2766 | INFO_REALIGN_3_PRIME | chr20 | 38577698 | ||||
| chr20:38577698
|
G | GACAC | 5 | a0001c0001t0003a0001c0001t0015a0001c0007t0003others(2): Show | 30 | HG00280.hp1 HG00738.hp1 HG01071.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2762_*2765dupACAC | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2766 | INFO_REALIGN_3_PRIME | chr20 | 38577698 | ||||
| chr20:38577698
|
G | GACACAC | 5 | a0001c0001t0020a0001c0001t0024a0001c0001t0027others(2): Show | 7 | HG02258.hp2 HG02622.hp1 HG02622.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2760_*2765dupACAC others(2): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2766 | INFO_REALIGN_3_PRIME | chr20 | 38577698 | ||||
| chr20:38577698
|
G | GACACACA others(1): Show |
3 | a0001c0001t0009a0001c0001t0022a0001c0003t0005 | 13 | HG02109.hp2 HG02451.hp1 HG02896.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2758_*2765dupACAC others(4): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2766 | INFO_REALIGN_3_PRIME | chr20 | 38577698 | ||||
| chr20:38577698
|
G | GACACACA others(3): Show |
3 | a0001c0001t0011a0001c0001t0021a0001c0003t0012 | 5 | HG01109.hp1 HG01361.hp1 HG02055.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2756_*2765dupACAC others(6): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2766 | INFO_REALIGN_3_PRIME | chr20 | 38577698 | ||||
| chr20:38577698
|
GAC | G | 2 | a0001c0001t0007a0001c0002t0007 | 4 | HG00642.hp2 HG00738.hp2 HG01433.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2764_*2765delAC | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2764 | INFO_REALIGN_3_PRIME | chr20 | 38577698 | ||||
| chr20:38577698
|
GACACAC | G | 2 | a0001c0001t0004a0001c0001t0023 | 12 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2760_*2765delACAC others(2): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2760 | INFO_REALIGN_3_PRIME | chr20 | 38577698 | ||||
| chr20:38577726
|
C | A | 1 | a0001c0001t0008 | 3 | HG02896.hp1 HG02897.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2759C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2759 | chr20 | 38577726 | |||||
| chr20:38577776
|
T | A | 7 | a0001c0001t0004a0001c0001t0009a0001c0001t0011others(4): Show | 20 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2809T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 2809 | chr20 | 38577776 | |||||
| chr20:38578046
|
AAAAT | A | 1 | a0001c0001t0006 | 7 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3098_*3101delATAA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 3098 | INFO_REALIGN_3_PRIME | chr20 | 38578046 | ||||
| chr20:38578341
|
G | T | 1 | a0001c0001t0019 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3374G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 3374 | chr20 | 38578341 | |||||
| chr20:38578601
|
T | G | 1 | a0001c0001t0018 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3634T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 3634 | chr20 | 38578601 | |||||
| chr20:38578738
|
G | C | 1 | a0001c0001t0017 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3771G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 30/30 | 3771 | chr20 | 38578738 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:38473165
|
C | T | 12 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(9): Show | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.-31+96C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38473165 | ||||||
| chr20:38473182
|
G | C | 3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-31+113G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38473182 | ||||||
| chr20:38473277
|
G | T | 1 | a0001c0001t0003g0200 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-31+208G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38473277 | ||||||
| chr20:38473325
|
C | T | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0003g0197 | 3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-31+256C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38473325 | ||||||
| chr20:38473368
|
T | G | 44 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0003g0197others(41): Show | 48 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(45): Show |
intron_variant | MODIFIER | c.-31+299T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38473368 | ||||||
| chr20:38473950
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-31+881G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38473950 | ||||||
| chr20:38474014
|
G | C | 40 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(37): Show | 44 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(41): Show |
intron_variant | MODIFIER | c.-31+945G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38474014 | ||||||
| chr20:38474057
|
C | A | 4 | a0001c0001t0001g0037a0001c0001t0003g0035a0001c0001t0003g0036others(1): Show | 4 | HG01071.hp2 HG01081.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.-31+988C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38474057 | ||||||
| chr20:38474081
|
G | C | 1 | a0001c0001t0020g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-31+1012G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38474081 | ||||||
| chr20:38474164
|
G | C | 152 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(149): Show | 158 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.-31+1095G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38474164 | ||||||
| chr20:38474243
|
G | A | 1 | a0001c0001t0001g0040 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-31+1174G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38474243 | ||||||
| chr20:38474269
|
G | A | 40 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(37): Show | 44 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(41): Show |
intron_variant | MODIFIER | c.-31+1200G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38474269 | ||||||
| chr20:38474435
|
C | G | 1 | a0001c0001t0001g0139 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-31+1366C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38474435 | ||||||
| chr20:38474681
|
C | A | 7 | a0001c0001t0006g0016a0001c0001t0009g0010a0001c0001t0009g0011others(4): Show | 7 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-31+1612C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38474681 | ||||||
| chr20:38474769
|
C | A | 1 | a0001c0001t0001g0140 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-31+1700C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38474769 | ||||||
| chr20:38474786
|
T | G | 6 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(3): Show | 7 | HG00642.hp1 HG02572.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-31+1717T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38474786 | ||||||
| chr20:38474885
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-31+1816C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38474885 | ||||||
| chr20:38474955
|
C | G | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137 | 3 | HG00741.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-31+1886C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38474955 | ||||||
| chr20:38475079
|
G | A | 4 | a0001c0001t0001g0041a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 4 | HG00741.hp2 HG02280.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+2010G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38475079 | ||||||
| chr20:38475089
|
G | A | 2 | a0001c0001t0021g0023a0001c0001t0022g0022 | 2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-31+2020G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38475089 | ||||||
| chr20:38475108
|
G | A | 40 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(37): Show | 44 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(41): Show |
intron_variant | MODIFIER | c.-31+2039G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38475108 | ||||||
| chr20:38475429
|
A | G | 14 | a0001c0002t0002g0122a0001c0002t0002g0123a0001c0002t0002g0124others(11): Show | 15 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.-31+2360A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38475429 | ||||||
| chr20:38475642
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-31+2573T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38475642 | ||||||
| chr20:38475717
|
C | T | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG03239.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-31+2648C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38475717 | ||||||
| chr20:38475813
|
C | T | 1 | a0001c0001t0019g0194 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-31+2744C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38475813 | ||||||
| chr20:38475928
|
C | A | 1 | a0001c0001t0003g0141 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-31+2859C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38475928 | ||||||
| chr20:38476073
|
G | T | 12 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(9): Show | 12 | NA18941.hp1 NA18949.hp1 NA18956.hp1 others(9): Show |
intron_variant | MODIFIER | c.-31+3004G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38476073 | ||||||
| chr20:38476156
|
G | A | 3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-31+3087G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38476156 | ||||||
| chr20:38476243
|
G | C | 1 | a0001c0001t0016g0043 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-31+3174G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38476243 | ||||||
| chr20:38476385
|
T | G | 2 | a0001c0001t0021g0023a0001c0001t0022g0022 | 2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-31+3316T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38476385 | ||||||
| chr20:38476461
|
C | G | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-31+3392C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38476461 | ||||||
| chr20:38476472
|
C | T | 1 | a0001c0001t0027g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-31+3403C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38476472 | ||||||
| chr20:38476586
|
T | C | 1 | a0001c0001t0027g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-31+3517T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38476586 | ||||||
| chr20:38476765
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-31+3696G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38476765 | ||||||
| chr20:38476783
|
G | T | 1 | a0001c0001t0002g0120 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-31+3714G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38476783 | ||||||
| chr20:38477514
|
C | A | 127 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(124): Show | 132 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.-31+4445C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38477514 | ||||||
| chr20:38477713
|
T | C | 6 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0012others(3): Show | 6 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31+4644T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38477713 | ||||||
| chr20:38477984
|
G | A | 1 | a0001c0003t0010g0201 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-31+4915G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38477984 | ||||||
| chr20:38478113
|
C | T | 1 | a0001c0001t0003g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-31+5044C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38478113 | ||||||
| chr20:38478200
|
C | T | 3 | a0001c0001t0001g0116a0001c0005t0001g0117a0001c0005t0001g0118 | 3 | NA19006.hp2 NA19059.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.-31+5131C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38478200 | ||||||
| chr20:38478295
|
G | A | 4 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(1): Show | 4 | HG00639.hp1 HG00741.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+5226G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38478295 | ||||||
| chr20:38478397
|
A | G | 1 | a0001c0001t0004g0021 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-31+5328A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38478397 | ||||||
| chr20:38478398
|
A | T | 150 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(147): Show | 156 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(153): Show |
intron_variant | MODIFIER | c.-31+5329A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38478398 | ||||||
| chr20:38478429
|
C | CT | 4 | a0001c0001t0001g0003a0001c0001t0001g0114a0001c0001t0001g0115others(1): Show | 5 | HG00735.hp2 HG01517.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.-31+5369dupT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 38478429 | |||||
| chr20:38478444
|
G | A | 1 | a0001c0001t0001g0184 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-31+5375G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38478444 | ||||||
| chr20:38478513
|
C | A | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0003g0197 | 3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-31+5444C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38478513 | ||||||
| chr20:38478531
|
C | G | 1 | a0001c0001t0002g0181 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-31+5462C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38478531 | ||||||
| chr20:38478582
|
G | A | 85 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(82): Show | 86 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.-31+5513G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38478582 | ||||||
| chr20:38478640
|
G | A | 20 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(17): Show | 21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-31+5571G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38478640 | ||||||
| chr20:38478678
|
G | A | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0003g0197 | 3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-31+5609G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38478678 | ||||||
| chr20:38478683
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-31+5614C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38478683 | ||||||
| chr20:38478773
|
C | T | 5 | a0001c0001t0006g0002a0001c0001t0006g0029a0001c0001t0006g0030others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-31+5704C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38478773 | ||||||
| chr20:38478786
|
T | C | 90 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(87): Show | 91 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.-31+5717T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38478786 | ||||||
| chr20:38478843
|
C | T | 7 | a0001c0001t0001g0041a0001c0001t0001g0135a0001c0001t0001g0136others(4): Show | 7 | HG00741.hp2 HG02280.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-31+5774C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38478843 | ||||||
| chr20:38479003
|
G | A | 1 | a0001c0001t0004g0024 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-31+5934G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38479003 | ||||||
| chr20:38479103
|
A | G | 87 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(84): Show | 88 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.-31+6034A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38479103 | ||||||
| chr20:38479113
|
C | CTACT | 2 | a0001c0001t0001g0112a0004c0010t0001g0111 | 2 | HG02004.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.-31+6045_-31+6048d others(6): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 38479113 | |||||
| chr20:38479737
|
G | A | 1 | a0001c0001t0003g0048 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-31+6668G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38479737 | ||||||
| chr20:38479738
|
A | T | 1 | a0001c0001t0003g0048 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-31+6669A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38479738 | ||||||
| chr20:38479739
|
T | C | 1 | a0001c0001t0003g0048 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-31+6670T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38479739 | ||||||
| chr20:38479935
|
A | G | 11 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(8): Show | 13 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-31+6866A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38479935 | ||||||
| chr20:38479994
|
T | G | 1 | a0001c0001t0003g0048 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-31+6925T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38479994 | ||||||
| chr20:38479996
|
G | T | 1 | a0001c0001t0003g0048 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-31+6927G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38479996 | ||||||
| chr20:38479998
|
T | G | 1 | a0001c0001t0003g0048 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-31+6929T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38479998 | ||||||
| chr20:38480011
|
T | G | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG03239.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-31+6942T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480011 | ||||||
| chr20:38480050
|
T | G | 1 | a0001c0001t0003g0048 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-31+6981T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480050 | ||||||
| chr20:38480262
|
C | T | 5 | a0001c0001t0006g0002a0001c0001t0006g0029a0001c0001t0006g0030others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-31+7193C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480262 | ||||||
| chr20:38480277
|
A | G | 20 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(17): Show | 21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-31+7208A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480277 | ||||||
| chr20:38480321
|
C | CT | 6 | a0001c0001t0001g0041a0001c0001t0001g0135a0001c0001t0001g0136others(3): Show | 7 | HG00642.hp2 HG00741.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.-31+7265dupT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 38480321 | |||||
| chr20:38480321
|
C | G | 1 | a0001c0001t0003g0048 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-31+7252C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480321 | ||||||
| chr20:38480321
|
CT | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(122): Show | 130 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.-31+7265delT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 38480321 | |||||
| chr20:38480322
|
T | C | 1 | a0001c0001t0003g0048 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-31+7253T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480322 | ||||||
| chr20:38480385
|
CTTTTTTT others(2): Show |
C | 87 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(84): Show | 88 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.-31+7327_-31+7335d others(11): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 38480385 | |||||
| chr20:38480389
|
T | C | 1 | a0001c0003t0005g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-31+7320T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480389 | ||||||
| chr20:38480426
|
A | C | 1 | a0001c0001t0003g0048 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-31+7357A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480426 | ||||||
| chr20:38480427
|
C | A | 1 | a0001c0001t0003g0048 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-31+7358C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480427 | ||||||
| chr20:38480539
|
A | C | 6 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0012others(3): Show | 6 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31+7470A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480539 | ||||||
| chr20:38480636
|
C | T | 12 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(9): Show | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.-31+7567C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480636 | ||||||
| chr20:38480735
|
G | C | 1 | a0001c0001t0002g0142 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-31+7666G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480735 | ||||||
| chr20:38480735
|
G | GC | 30 | a0001c0001t0001g0041a0001c0001t0001g0051a0001c0001t0001g0054others(27): Show | 30 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.-30-7660dupC | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 38480735 | |||||
| chr20:38480744
|
T | C | 3 | a0001c0001t0001g0119a0001c0001t0015g0050a0001c0008t0001g0049 | 3 | HG01081.hp1 HG01106.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.-30-7659T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480744 | ||||||
| chr20:38480760
|
C | T | 89 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(86): Show | 90 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.-30-7643C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480760 | ||||||
| chr20:38480761
|
G | A | 14 | a0001c0002t0002g0122a0001c0002t0002g0123a0001c0002t0002g0124others(11): Show | 15 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.-30-7642G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480761 | ||||||
| chr20:38480783
|
G | A | 14 | a0001c0002t0002g0122a0001c0002t0002g0123a0001c0002t0002g0124others(11): Show | 15 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.-30-7620G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480783 | ||||||
| chr20:38480841
|
C | T | 86 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(83): Show | 87 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.-30-7562C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480841 | ||||||
| chr20:38480878
|
C | T | 20 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(17): Show | 21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-30-7525C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480878 | ||||||
| chr20:38480882
|
C | T | 1 | a0001c0001t0024g0015 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-30-7521C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480882 | ||||||
| chr20:38480884
|
T | C | 151 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(148): Show | 157 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.-30-7519T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480884 | ||||||
| chr20:38480885
|
G | A | 5 | a0001c0001t0006g0002a0001c0001t0006g0029a0001c0001t0006g0030others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30-7518G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480885 | ||||||
| chr20:38480941
|
C | T | 3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-30-7462C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38480941 | ||||||
| chr20:38481159
|
G | T | 6 | a0001c0001t0001g0063a0001c0001t0001g0106a0001c0001t0003g0107others(3): Show | 6 | HG00639.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-30-7244G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38481159 | ||||||
| chr20:38481279
|
G | C | 1 | a0001c0001t0001g0051 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-30-7124G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38481279 | ||||||
| chr20:38481431
|
A | G | 12 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(9): Show | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.-30-6972A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38481431 | ||||||
| chr20:38481459
|
C | T | 20 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(17): Show | 21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-30-6944C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38481459 | ||||||
| chr20:38481974
|
T | A | 5 | a0001c0001t0006g0002a0001c0001t0006g0029a0001c0001t0006g0030others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30-6429T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38481974 | ||||||
| chr20:38482014
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-30-6389A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38482014 | ||||||
| chr20:38482019
|
T | TTCAAGTA others(308): Show |
3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-30-6371_-30-6370i others(317): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 38482019 | |||||
| chr20:38482158
|
T | C | 127 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(124): Show | 132 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.-30-6245T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38482158 | ||||||
| chr20:38482426
|
C | CT | 11 | a0001c0001t0001g0041a0001c0001t0001g0044a0001c0001t0001g0135others(8): Show | 11 | HG00639.hp1 HG00741.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.-30-5958dupT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 38482426 | |||||
| chr20:38482426
|
C | CTT | 94 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0042others(91): Show | 97 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.-30-5959_-30-5958d others(4): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 38482426 | |||||
| chr20:38482426
|
CT | C | 17 | a0001c0001t0001g0146a0001c0001t0002g0145a0001c0001t0004g0024others(14): Show | 18 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.-30-5958delT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 38482426 | |||||
| chr20:38482745
|
T | C | 4 | a0001c0001t0001g0041a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 4 | HG00741.hp2 HG02280.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30-5658T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38482745 | ||||||
| chr20:38483006
|
C | G | 4 | a0001c0001t0001g0041a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 4 | HG00741.hp2 HG02280.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30-5397C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38483006 | ||||||
| chr20:38483032
|
G | A | 1 | a0001c0001t0002g0147 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-30-5371G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38483032 | ||||||
| chr20:38483153
|
T | A | 20 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(17): Show | 21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-30-5250T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38483153 | ||||||
| chr20:38483159
|
G | T | 1 | a0001c0001t0026g0113 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-30-5244G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38483159 | ||||||
| chr20:38483316
|
C | G | 2 | a0001c0003t0005g0210a0001c0003t0012g0006 | 3 | HG01109.hp1 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-30-5087C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38483316 | ||||||
| chr20:38483413
|
A | G | 3 | a0001c0001t0004g0025a0001c0001t0004g0027a0001c0001t0004g0028 | 3 | HG02055.hp2 HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-30-4990A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38483413 | ||||||
| chr20:38483440
|
T | C | 20 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(17): Show | 21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-30-4963T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38483440 | ||||||
| chr20:38483471
|
T | C | 99 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(96): Show | 102 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.-30-4932T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38483471 | ||||||
| chr20:38483575
|
A | C | 14 | a0001c0002t0002g0122a0001c0002t0002g0123a0001c0002t0002g0124others(11): Show | 15 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.-30-4828A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38483575 | ||||||
| chr20:38483814
|
G | A | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-30-4589G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38483814 | ||||||
| chr20:38483975
|
G | A | 8 | a0001c0001t0001g0065a0001c0001t0001g0116a0001c0001t0001g0138others(5): Show | 8 | HG01106.hp2 HG02056.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-30-4428G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38483975 | ||||||
| chr20:38484052
|
G | A | 20 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(17): Show | 21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-30-4351G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38484052 | ||||||
| chr20:38484116
|
C | G | 22 | a0001c0001t0001g0041a0001c0001t0001g0135a0001c0001t0001g0136others(19): Show | 23 | HG00642.hp2 HG00741.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.-30-4287C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38484116 | ||||||
| chr20:38484135
|
G | A | 1 | a0001c0001t0027g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-30-4268G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38484135 | ||||||
| chr20:38484292
|
A | G | 99 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(96): Show | 102 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.-30-4111A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38484292 | ||||||
| chr20:38484319
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-30-4084G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38484319 | ||||||
| chr20:38484604
|
G | A | 2 | a0001c0003t0005g0210a0001c0003t0012g0006 | 3 | HG01109.hp1 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-30-3799G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38484604 | ||||||
| chr20:38485119
|
A | G | 1 | a0001c0001t0026g0113 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-30-3284A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38485119 | ||||||
| chr20:38485211
|
T | G | 1 | a0001c0007t0003g0067 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-30-3192T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38485211 | ||||||
| chr20:38485243
|
G | T | 90 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(87): Show | 91 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.-30-3160G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38485243 | ||||||
| chr20:38485320
|
A | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0103 | 2 | HG03492.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-30-3083A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38485320 | ||||||
| chr20:38485320
|
A | T | 1 | a0001c0001t0003g0104 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-30-3083A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38485320 | ||||||
| chr20:38485544
|
G | A | 6 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0069others(3): Show | 6 | HG01361.hp2 HG02602.hp2 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30-2859G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38485544 | ||||||
| chr20:38485761
|
G | A | 1 | a0001c0001t0020g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-30-2642G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38485761 | ||||||
| chr20:38485966
|
C | CT | 178 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0037others(175): Show | 184 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(181): Show |
intron_variant | MODIFIER | c.-30-2417dupT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 38485966 | |||||
| chr20:38485966
|
C | CTT | 7 | a0001c0001t0001g0047a0001c0001t0003g0110a0001c0001t0003g0192others(4): Show | 7 | HG00741.hp1 HG01243.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30-2418_-30-2417d others(4): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 38485966 | |||||
| chr20:38486008
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-30-2395C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38486008 | ||||||
| chr20:38486026
|
A | G | 2 | a0001c0001t0001g0074a0001c0001t0003g0182 | 2 | NA18986.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-30-2377A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38486026 | ||||||
| chr20:38486070
|
C | T | 2 | a0001c0003t0005g0210a0001c0003t0012g0006 | 3 | HG01109.hp1 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-30-2333C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38486070 | ||||||
| chr20:38486264
|
C | T | 1 | a0001c0001t0003g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-30-2139C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38486264 | ||||||
| chr20:38486792
|
C | G | 1 | a0001c0001t0001g0102 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-30-1611C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38486792 | ||||||
| chr20:38486889
|
A | G | 32 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(29): Show | 35 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(32): Show |
intron_variant | MODIFIER | c.-30-1514A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38486889 | ||||||
| chr20:38487242
|
T | C | 3 | a0001c0001t0001g0077a0001c0001t0003g0076a0001c0012t0001g0075 | 3 | NA18977.hp1 NA18999.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-30-1161T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38487242 | ||||||
| chr20:38487248
|
G | A | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-30-1155G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38487248 | ||||||
| chr20:38487334
|
A | AT | 128 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(125): Show | 133 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.-30-1060dupT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 38487334 | |||||
| chr20:38487430
|
C | T | 2 | a0001c0001t0001g0139a0001c0001t0028g0066 | 2 | HG01106.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.-30-973C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38487430 | ||||||
| chr20:38487512
|
G | A | 1 | a0001c0001t0020g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-30-891G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38487512 | ||||||
| chr20:38487522
|
T | C | 1 | a0001c0001t0003g0048 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-30-881T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38487522 | ||||||
| chr20:38487705
|
A | C | 12 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(9): Show | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.-30-698A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38487705 | ||||||
| chr20:38487755
|
A | T | 1 | a0001c0001t0003g0061 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-30-648A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38487755 | ||||||
| chr20:38487837
|
C | T | 5 | a0001c0001t0006g0002a0001c0001t0006g0029a0001c0001t0006g0030others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30-566C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38487837 | ||||||
| chr20:38487921
|
T | C | 150 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(147): Show | 156 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(153): Show |
intron_variant | MODIFIER | c.-30-482T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38487921 | ||||||
| chr20:38487930
|
G | A | 87 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(84): Show | 88 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.-30-473G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38487930 | ||||||
| chr20:38488067
|
G | GA | 7 | a0001c0001t0006g0016a0001c0001t0009g0010a0001c0001t0009g0011others(4): Show | 7 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30-328dupA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 38488067 | |||||
| chr20:38488148
|
C | T | 1 | a0001c0001t0003g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-30-255C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38488148 | ||||||
| chr20:38488211
|
C | G | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0003g0197 | 3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-30-192C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38488211 | ||||||
| chr20:38488279
|
C | T | 12 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(9): Show | 13 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-30-124C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 1/29 | chr20 | 38488279 | ||||||
| chr20:38488758
|
C | G | 1 | a0001c0001t0001g0055 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.186+140C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38488758 | ||||||
| chr20:38488928
|
A | G | 1 | a0001c0001t0004g0021 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.186+310A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38488928 | ||||||
| chr20:38489651
|
A | G | 1 | a0001c0001t0004g0019 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.186+1033A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38489651 | ||||||
| chr20:38489815
|
A | G | 5 | a0001c0001t0006g0002a0001c0001t0006g0029a0001c0001t0006g0030others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.186+1197A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38489815 | ||||||
| chr20:38489837
|
G | A | 14 | a0001c0002t0002g0122a0001c0002t0002g0123a0001c0002t0002g0124others(11): Show | 15 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.186+1219G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38489837 | ||||||
| chr20:38490011
|
CT | C | 5 | a0001c0001t0001g0055a0001c0001t0002g0161a0001c0001t0002g0162others(2): Show | 5 | HG02809.hp2 NA18974.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.186+1409delT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr20 | 38490011 | |||||
| chr20:38490033
|
G | A | 12 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(9): Show | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.186+1415G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38490033 | ||||||
| chr20:38490080
|
G | A | 1 | a0001c0001t0007g0163 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.186+1462G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38490080 | ||||||
| chr20:38490100
|
C | T | 5 | a0001c0001t0006g0002a0001c0001t0006g0029a0001c0001t0006g0030others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.186+1482C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38490100 | ||||||
| chr20:38490301
|
C | T | 1 | a0001c0001t0020g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.186+1683C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38490301 | ||||||
| chr20:38490334
|
G | A | 1 | a0001c0001t0003g0035 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.186+1716G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38490334 | ||||||
| chr20:38490507
|
C | G | 1 | a0001c0001t0001g0065 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.186+1889C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38490507 | ||||||
| chr20:38490511
|
T | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0047 | 2 | HG00741.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.186+1893T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38490511 | ||||||
| chr20:38490650
|
GCATGCAC others(69): Show |
G | 5 | a0001c0001t0006g0002a0001c0001t0006g0029a0001c0001t0006g0030others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.186+2034_186+2109d others(78): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr20 | 38490650 | |||||
| chr20:38490803
|
C | T | 3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.187-2127C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38490803 | ||||||
| chr20:38491013
|
A | G | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.187-1917A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38491013 | ||||||
| chr20:38491032
|
C | G | 1 | a0005c0011t0002g0160 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.187-1898C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38491032 | ||||||
| chr20:38491044
|
C | G | 6 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0012others(3): Show | 6 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.187-1886C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38491044 | ||||||
| chr20:38491324
|
A | T | 3 | a0001c0001t0002g0177a0001c0001t0002g0178a0001c0001t0002g0179 | 3 | HG02257.hp1 HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.187-1606A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38491324 | ||||||
| chr20:38491333
|
C | CT | 6 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0012others(3): Show | 6 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.187-1586dupT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr20 | 38491333 | |||||
| chr20:38491333
|
CT | C | 9 | a0001c0001t0002g0142a0001c0001t0002g0143a0001c0001t0002g0145others(6): Show | 9 | HG00280.hp2 HG00735.hp1 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.187-1586delT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr20 | 38491333 | |||||
| chr20:38491539
|
T | C | 1 | a0001c0001t0006g0029 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.187-1391T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38491539 | ||||||
| chr20:38491638
|
G | T | 1 | a0001c0001t0006g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.187-1292G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38491638 | ||||||
| chr20:38491927
|
C | T | 1 | a0001c0001t0002g0147 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.187-1003C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38491927 | ||||||
| chr20:38492839
|
G | T | 1 | a0001c0001t0006g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.187-91G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 2/29 | chr20 | 38492839 | ||||||
| chr20:38493171
|
A | C | 1 | a0001c0001t0001g0140 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.389+39A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38493171 | ||||||
| chr20:38493826
|
G | T | 5 | a0001c0001t0006g0002a0001c0001t0006g0029a0001c0001t0006g0030others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.389+694G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38493826 | ||||||
| chr20:38494144
|
C | T | 1 | a0001c0001t0002g0053 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.389+1012C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38494144 | ||||||
| chr20:38494220
|
C | G | 2 | a0001c0001t0001g0055a0001c0001t0001g0071 | 2 | NA18974.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.389+1088C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38494220 | ||||||
| chr20:38494387
|
T | C | 1 | a0001c0001t0001g0065 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.389+1255T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38494387 | ||||||
| chr20:38494537
|
AG | A | 6 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0012others(3): Show | 6 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.389+1407delG | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr20 | 38494537 | |||||
| chr20:38494580
|
G | A | 6 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0012others(3): Show | 6 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.389+1448G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38494580 | ||||||
| chr20:38494585
|
T | A | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.389+1453T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38494585 | ||||||
| chr20:38494760
|
A | G | 32 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(29): Show | 35 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(32): Show |
intron_variant | MODIFIER | c.389+1628A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38494760 | ||||||
| chr20:38494762
|
G | T | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.389+1630G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38494762 | ||||||
| chr20:38494809
|
T | C | 4 | a0001c0001t0001g0041a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 4 | HG00741.hp2 HG02280.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.389+1677T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38494809 | ||||||
| chr20:38495187
|
A | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0103 | 2 | HG03492.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.389+2055A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38495187 | ||||||
| chr20:38495466
|
T | C | 8 | a0001c0001t0002g0147a0001c0001t0002g0161a0001c0001t0002g0162others(5): Show | 8 | HG01109.hp2 HG01978.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.390-1887T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38495466 | ||||||
| chr20:38495710
|
G | T | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.390-1643G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38495710 | ||||||
| chr20:38495927
|
T | C | 1 | a0001c0001t0006g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.390-1426T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38495927 | ||||||
| chr20:38496038
|
A | G | 1 | a0001c0001t0003g0061 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.390-1315A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38496038 | ||||||
| chr20:38496242
|
G | C | 5 | a0001c0001t0006g0002a0001c0001t0006g0029a0001c0001t0006g0030others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.390-1111G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38496242 | ||||||
| chr20:38496265
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.390-1088C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38496265 | ||||||
| chr20:38496736
|
T | G | 1 | a0001c0001t0003g0058 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.390-617T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38496736 | ||||||
| chr20:38496749
|
A | G | 1 | a0001c0001t0003g0038 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.390-604A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38496749 | ||||||
| chr20:38496897
|
T | G | 2 | a0001c0001t0001g0063a0001c0001t0001g0106 | 2 | HG00639.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.390-456T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38496897 | ||||||
| chr20:38497197
|
T | G | 1 | a0001c0001t0001g0042 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.390-156T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38497197 | ||||||
| chr20:38497214
|
C | T | 87 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(84): Show | 88 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.390-139C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 3/29 | chr20 | 38497214 | ||||||
| chr20:38497802
|
G | A | 5 | a0001c0001t0002g0147a0001c0001t0002g0165a0001c0001t0002g0166others(2): Show | 5 | HG01109.hp2 HG01978.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.553+286G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 4/29 | chr20 | 38497802 | ||||||
| chr20:38497889
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.553+373C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 4/29 | chr20 | 38497889 | ||||||
| chr20:38498069
|
C | CA | 110 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(107): Show | 114 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.553+569dupA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 38498069 | |||||
| chr20:38498069
|
C | CAA | 5 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0109others(2): Show | 5 | HG02572.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.553+568_553+569dup others(2): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 38498069 | |||||
| chr20:38498083
|
AAAG | A | 5 | a0001c0001t0006g0002a0001c0001t0006g0029a0001c0001t0006g0030others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.553+570_553+572del others(3): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 38498083 | |||||
| chr20:38498095
|
CAATT | C | 8 | a0001c0001t0003g0035a0001c0001t0003g0036a0001c0001t0003g0038others(5): Show | 8 | HG00280.hp1 HG00738.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.553+582_553+585del others(4): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 38498095 | |||||
| chr20:38498169
|
G | A | 5 | a0001c0001t0001g0116a0001c0001t0001g0139a0001c0001t0028g0066others(2): Show | 5 | HG01106.hp2 HG02071.hp1 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.553+653G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 4/29 | chr20 | 38498169 | ||||||
| chr20:38498619
|
C | T | 5 | a0001c0001t0006g0002a0001c0001t0006g0029a0001c0001t0006g0030others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.554-828C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 4/29 | chr20 | 38498619 | ||||||
| chr20:38498708
|
C | T | 12 | a0001c0002t0002g0122a0001c0002t0002g0123a0001c0002t0002g0124others(9): Show | 13 | HG00642.hp2 HG01433.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.554-739C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 4/29 | chr20 | 38498708 | ||||||
| chr20:38498794
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.554-653A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 4/29 | chr20 | 38498794 | ||||||
| chr20:38498812
|
A | G | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0003g0197 | 3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.554-635A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 4/29 | chr20 | 38498812 | ||||||
| chr20:38499272
|
G | C | 3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.554-175G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 4/29 | chr20 | 38499272 | ||||||
| chr20:38499437
|
T | C | 17 | a0001c0001t0006g0002a0001c0001t0006g0029a0001c0001t0006g0030others(14): Show | 20 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.554-10T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 4/29 | chr20 | 38499437 | ||||||
| chr20:38499641
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02280.hp1 | splice_region_variant&intron_variant | LOW | c.740+8A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38499641 | ||||||
| chr20:38499686
|
T | A | 1 | a0001c0001t0006g0030 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.740+53T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38499686 | ||||||
| chr20:38499894
|
A | G | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.740+261A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38499894 | ||||||
| chr20:38499922
|
G | C | 2 | a0001c0001t0021g0023a0001c0001t0022g0022 | 2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.740+289G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38499922 | ||||||
| chr20:38499961
|
A | G | 7 | a0001c0001t0001g0065a0001c0001t0001g0116a0001c0001t0001g0139others(4): Show | 7 | HG01106.hp2 HG02056.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.740+328A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38499961 | ||||||
| chr20:38500132
|
T | G | 5 | a0001c0001t0006g0002a0001c0001t0006g0029a0001c0001t0006g0030others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.740+499T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38500132 | ||||||
| chr20:38500173
|
C | A | 1 | a0002c0004t0030g0007 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.740+540C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38500173 | ||||||
| chr20:38500174
|
G | C | 127 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(124): Show | 132 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.740+541G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38500174 | ||||||
| chr20:38500254
|
T | C | 1 | a0001c0003t0010g0202 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.740+621T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38500254 | ||||||
| chr20:38500300
|
G | C | 1 | a0001c0001t0003g0079 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.740+667G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38500300 | ||||||
| chr20:38500598
|
G | T | 122 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(119): Show | 126 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.740+965G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38500598 | ||||||
| chr20:38500961
|
G | C | 2 | a0001c0001t0021g0023a0001c0001t0022g0022 | 2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.740+1328G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38500961 | ||||||
| chr20:38501023
|
C | T | 3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.740+1390C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38501023 | ||||||
| chr20:38501041
|
A | G | 12 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(9): Show | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.740+1408A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38501041 | ||||||
| chr20:38501103
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.740+1470C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38501103 | ||||||
| chr20:38501105
|
A | C | 1 | a0001c0001t0001g0070 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.740+1472A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38501105 | ||||||
| chr20:38501338
|
G | T | 12 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(9): Show | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.740+1705G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38501338 | ||||||
| chr20:38501365
|
A | G | 13 | a0001c0001t0001g0041a0001c0001t0001g0135a0001c0001t0001g0136others(10): Show | 14 | HG00741.hp2 HG01884.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.740+1732A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38501365 | ||||||
| chr20:38501430
|
G | A | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137 | 3 | HG00741.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.740+1797G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38501430 | ||||||
| chr20:38501437
|
G | C | 36 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(33): Show | 39 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(36): Show |
intron_variant | MODIFIER | c.740+1804G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38501437 | ||||||
| chr20:38501488
|
C | T | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137 | 3 | HG00741.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.740+1855C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38501488 | ||||||
| chr20:38501683
|
G | C | 1 | a0001c0001t0026g0113 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.740+2050G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38501683 | ||||||
| chr20:38501703
|
C | T | 12 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(9): Show | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.740+2070C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38501703 | ||||||
| chr20:38501958
|
C | T | 152 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(149): Show | 158 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.740+2325C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38501958 | ||||||
| chr20:38501994
|
A | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0114a0001c0001t0001g0115 | 4 | HG00735.hp2 HG01517.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.740+2361A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38501994 | ||||||
| chr20:38502000
|
T | C | 1 | a0001c0001t0001g0119 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.740+2367T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38502000 | ||||||
| chr20:38502048
|
G | A | 3 | a0001c0001t0001g0077a0001c0001t0003g0076a0001c0012t0001g0075 | 3 | NA18977.hp1 NA18999.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.740+2415G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38502048 | ||||||
| chr20:38502171
|
A | G | 5 | a0001c0001t0006g0002a0001c0001t0006g0029a0001c0001t0006g0030others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.740+2538A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38502171 | ||||||
| chr20:38502205
|
G | A | 2 | a0001c0001t0001g0077a0001c0012t0001g0075 | 2 | NA18977.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.740+2572G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38502205 | ||||||
| chr20:38502208
|
A | C | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.740+2575A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38502208 | ||||||
| chr20:38502542
|
A | G | 1 | a0001c0001t0027g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.740+2909A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38502542 | ||||||
| chr20:38502592
|
A | AT | 12 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(9): Show | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.740+2968dupT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr20 | 38502592 | |||||
| chr20:38502667
|
C | T | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.740+3034C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38502667 | ||||||
| chr20:38502848
|
G | A | 20 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(17): Show | 21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.740+3215G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38502848 | ||||||
| chr20:38502978
|
C | T | 1 | a0001c0001t0002g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.740+3345C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38502978 | ||||||
| chr20:38503019
|
C | T | 5 | a0001c0001t0006g0002a0001c0001t0006g0029a0001c0001t0006g0030others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.740+3386C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38503019 | ||||||
| chr20:38503078
|
A | C | 87 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(84): Show | 88 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.740+3445A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38503078 | ||||||
| chr20:38503239
|
A | C | 3 | a0001c0001t0002g0158a0001c0001t0002g0159a0001c0001t0002g0176 | 3 | NA18973.hp1 NA19012.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.740+3606A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38503239 | ||||||
| chr20:38503409
|
C | G | 2 | a0001c0001t0021g0023a0001c0001t0022g0022 | 2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.740+3776C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38503409 | ||||||
| chr20:38503820
|
A | AT | 5 | a0001c0001t0006g0002a0001c0001t0006g0029a0001c0001t0006g0030others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.740+4192dupT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr20 | 38503820 | |||||
| chr20:38503961
|
A | G | 5 | a0001c0001t0006g0002a0001c0001t0006g0029a0001c0001t0006g0030others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.740+4328A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38503961 | ||||||
| chr20:38504034
|
G | A | 3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.740+4401G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38504034 | ||||||
| chr20:38504194
|
T | C | 1 | a0001c0001t0020g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.740+4561T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38504194 | ||||||
| chr20:38504305
|
CAG | C | 20 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(17): Show | 21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.740+4675_740+4676d others(4): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr20 | 38504305 | |||||
| chr20:38504319
|
A | G | 87 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(84): Show | 88 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.740+4686A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38504319 | ||||||
| chr20:38504340
|
C | G | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0003g0197 | 3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.740+4707C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38504340 | ||||||
| chr20:38504381
|
T | C | 1 | a0001c0001t0001g0080 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.741-4696T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38504381 | ||||||
| chr20:38504476
|
A | G | 87 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(84): Show | 88 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.741-4601A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38504476 | ||||||
| chr20:38504577
|
A | G | 1 | a0001c0001t0006g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.741-4500A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38504577 | ||||||
| chr20:38505049
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.741-4028A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38505049 | ||||||
| chr20:38505185
|
G | A | 1 | a0001c0001t0007g0163 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.741-3892G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38505185 | ||||||
| chr20:38505215
|
G | A | 7 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(4): Show | 8 | HG02451.hp1 HG02922.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.741-3862G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38505215 | ||||||
| chr20:38505228
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.741-3849A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38505228 | ||||||
| chr20:38505505
|
A | G | 1 | a0001c0001t0023g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.741-3572A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38505505 | ||||||
| chr20:38505636
|
AT | A | 20 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(17): Show | 21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.741-3436delT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr20 | 38505636 | |||||
| chr20:38505661
|
A | G | 1 | a0001c0001t0003g0104 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.741-3416A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38505661 | ||||||
| chr20:38505793
|
G | A | 7 | a0001c0001t0001g0041a0001c0001t0001g0135a0001c0001t0001g0136others(4): Show | 7 | HG00741.hp2 HG02280.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.741-3284G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38505793 | ||||||
| chr20:38505942
|
G | A | 20 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(17): Show | 21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.741-3135G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38505942 | ||||||
| chr20:38505995
|
C | A | 1 | a0001c0001t0001g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.741-3082C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38505995 | ||||||
| chr20:38506056
|
ACTGC | A | 149 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(146): Show | 155 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(152): Show |
intron_variant | MODIFIER | c.741-3017_741-3014d others(6): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr20 | 38506056 | |||||
| chr20:38506248
|
A | G | 3 | a0001c0001t0006g0016a0001c0001t0021g0023a0001c0001t0022g0022 | 3 | HG02055.hp1 HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.741-2829A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38506248 | ||||||
| chr20:38506306
|
T | G | 1 | a0001c0001t0001g0188 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.741-2771T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38506306 | ||||||
| chr20:38507294
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.741-1783C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38507294 | ||||||
| chr20:38507614
|
A | G | 7 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(4): Show | 8 | HG00642.hp1 HG01884.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.741-1463A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38507614 | ||||||
| chr20:38507682
|
G | A | 1 | a0001c0001t0003g0079 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.741-1395G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38507682 | ||||||
| chr20:38507700
|
T | G | 87 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(84): Show | 88 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.741-1377T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38507700 | ||||||
| chr20:38507706
|
T | C | 5 | a0001c0001t0006g0002a0001c0001t0006g0029a0001c0001t0006g0030others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.741-1371T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38507706 | ||||||
| chr20:38508082
|
CTT | C | 12 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(9): Show | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.741-992_741-991del others(2): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr20 | 38508082 | |||||
| chr20:38508105
|
A | G | 6 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0012others(3): Show | 6 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.741-972A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38508105 | ||||||
| chr20:38508168
|
C | T | 63 | a0001c0001t0001g0041a0001c0001t0001g0135a0001c0001t0001g0136others(60): Show | 68 | HG00642.hp1 HG00642.hp2 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.741-909C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38508168 | ||||||
| chr20:38508196
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.741-881A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38508196 | ||||||
| chr20:38508242
|
T | C | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0002g0155 | 3 | HG03491.hp1 HG03492.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.741-835T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38508242 | ||||||
| chr20:38508326
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.741-751A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38508326 | ||||||
| chr20:38508552
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.741-525A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38508552 | ||||||
| chr20:38508601
|
T | C | 4 | a0001c0001t0004g0024a0001c0001t0004g0025a0001c0001t0004g0027others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.741-476T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38508601 | ||||||
| chr20:38508847
|
A | T | 3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.741-230A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38508847 | ||||||
| chr20:38509017
|
C | A | 3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.741-60C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 5/29 | chr20 | 38509017 | ||||||
| chr20:38509379
|
C | T | 1 | a0001c0001t0027g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.872+171C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38509379 | ||||||
| chr20:38509456
|
G | A | 1 | a0001c0001t0002g0161 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.872+248G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38509456 | ||||||
| chr20:38509548
|
C | T | 20 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(17): Show | 21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.872+340C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38509548 | ||||||
| chr20:38509748
|
T | C | 5 | a0001c0001t0006g0002a0001c0001t0006g0029a0001c0001t0006g0030others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.872+540T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38509748 | ||||||
| chr20:38509786
|
T | C | 1 | a0001c0001t0001g0081 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.872+578T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38509786 | ||||||
| chr20:38510131
|
T | TAC | 7 | a0001c0001t0001g0034a0001c0001t0001g0055a0001c0001t0001g0140others(4): Show | 7 | HG02015.hp2 HG02071.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.872+957_872+958dup others(2): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38510131 | |||||
| chr20:38510131
|
TAC | T | 54 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(51): Show | 55 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.872+957_872+958del others(2): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38510131 | |||||
| chr20:38510131
|
TACAC | T | 15 | a0001c0001t0001g0041a0001c0001t0001g0060a0001c0001t0001g0073others(12): Show | 15 | HG00741.hp2 HG01255.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.872+955_872+958del others(4): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38510131 | |||||
| chr20:38510131
|
TACACAC | T | 52 | a0001c0001t0001g0119a0001c0001t0002g0095a0001c0001t0002g0168others(49): Show | 56 | HG00642.hp1 HG00642.hp2 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.872+953_872+958del others(6): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38510131 | |||||
| chr20:38510131
|
TACACACA others(7): Show |
T | 1 | a0001c0001t0020g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.872+945_872+958del others(14): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38510131 | |||||
| chr20:38510131
|
TACACACA others(9): Show |
T | 4 | a0001c0001t0006g0002a0001c0001t0006g0029a0001c0001t0006g0030others(1): Show | 5 | HG01884.hp2 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.872+943_872+958del others(16): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38510131 | |||||
| chr20:38510131
|
TACACACA others(11): Show |
T | 1 | a0001c0001t0006g0032 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.872+941_872+958del others(18): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38510131 | |||||
| chr20:38510144
|
A | G | 14 | a0001c0002t0002g0122a0001c0002t0002g0123a0001c0002t0002g0124others(11): Show | 15 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.872+936A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38510144 | ||||||
| chr20:38510165
|
CAG | C | 3 | a0001c0001t0001g0072a0001c0001t0001g0098a0001c0001t0025g0097 | 3 | HG01243.hp1 HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.872+959_872+960del others(2): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38510165 | |||||
| chr20:38510613
|
TGAAAATC others(306): Show |
T | 40 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(37): Show | 44 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(41): Show |
intron_variant | MODIFIER | c.872+1420_872+1732d others(2): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38510613 | |||||
| chr20:38510638
|
C | T | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0003g0197 | 3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.872+1430C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38510638 | ||||||
| chr20:38510925
|
A | C | 4 | a0001c0001t0002g0158a0001c0001t0002g0159a0001c0001t0002g0176others(1): Show | 4 | HG03669.hp2 NA18973.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.872+1717A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38510925 | ||||||
| chr20:38510957
|
C | T | 1 | a0001c0001t0003g0094 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.872+1749C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38510957 | ||||||
| chr20:38511042
|
T | C | 5 | a0001c0001t0002g0147a0001c0001t0002g0165a0001c0001t0002g0166others(2): Show | 5 | HG01109.hp2 HG01978.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.872+1834T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38511042 | ||||||
| chr20:38511082
|
CAG | C | 3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.872+1879_872+1880d others(4): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38511082 | |||||
| chr20:38511321
|
CT | C | 18 | a0001c0001t0001g0056a0001c0001t0001g0153a0001c0001t0006g0030others(15): Show | 19 | HG01069.hp1 HG01884.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.872+2127delT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38511321 | |||||
| chr20:38511385
|
G | C | 3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.872+2177G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38511385 | ||||||
| chr20:38511577
|
A | G | 1 | a0001c0012t0001g0075 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.872+2369A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38511577 | ||||||
| chr20:38511858
|
C | CG | 4 | a0001c0001t0001g0112a0001c0001t0001g0137a0001c0001t0004g0019others(1): Show | 4 | HG00741.hp2 HG02004.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.872+2654dupG | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38511858 | |||||
| chr20:38511867
|
G | A | 12 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(9): Show | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.872+2659G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38511867 | ||||||
| chr20:38511871
|
G | T | 6 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0012others(3): Show | 6 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.872+2663G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38511871 | ||||||
| chr20:38511903
|
C | T | 6 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0012others(3): Show | 6 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.872+2695C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38511903 | ||||||
| chr20:38512256
|
C | T | 2 | a0001c0001t0021g0023a0001c0001t0022g0022 | 2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.872+3048C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38512256 | ||||||
| chr20:38512319
|
T | C | 1 | a0001c0001t0006g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.872+3111T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38512319 | ||||||
| chr20:38512496
|
A | C | 20 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(17): Show | 21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.872+3288A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38512496 | ||||||
| chr20:38512623
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.872+3415G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38512623 | ||||||
| chr20:38512782
|
T | C | 37 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(34): Show | 41 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(38): Show |
intron_variant | MODIFIER | c.873-3410T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38512782 | ||||||
| chr20:38512791
|
G | A | 1 | a0001c0001t0002g0177 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.873-3401G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38512791 | ||||||
| chr20:38512935
|
A | AT | 12 | a0001c0001t0001g0041a0001c0001t0001g0135a0001c0001t0001g0136others(9): Show | 13 | HG00741.hp2 HG01884.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.873-3251dupT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38512935 | |||||
| chr20:38513055
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.873-3137C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513055 | ||||||
| chr20:38513137
|
G | A | 3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.873-3055G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513137 | ||||||
| chr20:38513138
|
C | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 4 | HG00741.hp2 HG02280.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.873-3054C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513138 | ||||||
| chr20:38513157
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.873-3035T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513157 | ||||||
| chr20:38513241
|
C | T | 12 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(9): Show | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.873-2951C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513241 | ||||||
| chr20:38513268
|
C | G | 1 | a0001c0001t0027g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.873-2924C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513268 | ||||||
| chr20:38513283
|
C | T | 4 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167others(1): Show | 4 | HG01109.hp2 HG01978.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.873-2909C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513283 | ||||||
| chr20:38513373
|
A | G | 2 | a0001c0003t0010g0201a0001c0003t0010g0209 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.873-2819A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513373 | ||||||
| chr20:38513453
|
C | T | 1 | a0001c0001t0003g0092 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.873-2739C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513453 | ||||||
| chr20:38513482
|
G | A | 4 | a0001c0001t0002g0147a0001c0001t0002g0165a0001c0001t0002g0166others(1): Show | 4 | HG01109.hp2 HG01978.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.873-2710G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513482 | ||||||
| chr20:38513482
|
G | C | 1 | a0001c0001t0027g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.873-2710G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513482 | ||||||
| chr20:38513503
|
T | C | 4 | a0001c0001t0004g0024a0001c0001t0004g0025a0001c0001t0004g0027others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.873-2689T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513503 | ||||||
| chr20:38513646
|
CA | C | 20 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(17): Show | 21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.873-2530delA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38513646 | |||||
| chr20:38513703
|
C | T | 1 | a0001c0001t0002g0152 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.873-2489C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513703 | ||||||
| chr20:38513799
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.873-2393C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513799 | ||||||
| chr20:38513822
|
T | C | 1 | a0001c0001t0002g0165 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.873-2370T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513822 | ||||||
| chr20:38513878
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.873-2314A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38513878 | ||||||
| chr20:38514010
|
TTAGA | T | 2 | a0001c0001t0021g0023a0001c0001t0022g0022 | 2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.873-2178_873-2175d others(6): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38514010 | |||||
| chr20:38514084
|
A | T | 1 | a0001c0002t0002g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.873-2108A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38514084 | ||||||
| chr20:38514198
|
C | T | 1 | a0001c0001t0002g0052 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.873-1994C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38514198 | ||||||
| chr20:38514432
|
G | A | 1 | a0001c0001t0027g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.873-1760G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38514432 | ||||||
| chr20:38514498
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.873-1694G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38514498 | ||||||
| chr20:38514529
|
C | T | 3 | a0001c0001t0004g0025a0001c0001t0004g0027a0001c0001t0004g0028 | 3 | HG02055.hp2 HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.873-1663C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38514529 | ||||||
| chr20:38514532
|
C | G | 208 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0037others(205): Show | 214 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(211): Show |
intron_variant | MODIFIER | c.873-1660C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38514532 | ||||||
| chr20:38515126
|
C | T | 9 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(6): Show | 10 | HG02451.hp1 HG02622.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.873-1066C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38515126 | ||||||
| chr20:38515164
|
C | T | 3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.873-1028C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38515164 | ||||||
| chr20:38515338
|
T | C | 1 | a0001c0001t0001g0184 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.873-854T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38515338 | ||||||
| chr20:38515507
|
CTGTT | C | 3 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0109 | 3 | HG02895.hp1 HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.873-681_873-678del others(4): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38515507 | |||||
| chr20:38515546
|
G | A | 1 | a0005c0011t0002g0160 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.873-646G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38515546 | ||||||
| chr20:38515648
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.873-544G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38515648 | ||||||
| chr20:38515717
|
CTTTTTCT others(1): Show |
C | 12 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(9): Show | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.873-452_873-445del others(8): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 38515717 | |||||
| chr20:38515758
|
A | G | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.873-434A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38515758 | ||||||
| chr20:38515851
|
A | C | 1 | a0001c0001t0004g0028 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.873-341A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38515851 | ||||||
| chr20:38515877
|
G | T | 1 | a0001c0001t0003g0092 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.873-315G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38515877 | ||||||
| chr20:38515884
|
C | G | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0003g0197 | 3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.873-308C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38515884 | ||||||
| chr20:38515984
|
G | C | 2 | a0001c0001t0001g0077a0001c0012t0001g0075 | 2 | NA18977.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.873-208G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38515984 | ||||||
| chr20:38516053
|
G | A | 12 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(9): Show | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.873-139G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 6/29 | chr20 | 38516053 | ||||||
| chr20:38516445
|
T | C | 1 | a0001c0001t0027g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1051+75T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 7/29 | chr20 | 38516445 | ||||||
| chr20:38516461
|
G | A | 12 | a0001c0002t0002g0122a0001c0002t0002g0123a0001c0002t0002g0124others(9): Show | 12 | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1051+91G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 7/29 | chr20 | 38516461 | ||||||
| chr20:38516495
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1051+125G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 7/29 | chr20 | 38516495 | ||||||
| chr20:38516643
|
T | A | 1 | a0001c0001t0001g0084 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1051+273T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 7/29 | chr20 | 38516643 | ||||||
| chr20:38516677
|
G | A | 1 | a0001c0001t0003g0068 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1051+307G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 7/29 | chr20 | 38516677 | ||||||
| chr20:38516710
|
T | C | 20 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(17): Show | 21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1051+340T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 7/29 | chr20 | 38516710 | ||||||
| chr20:38516871
|
T | C | 1 | a0001c0001t0004g0025 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1051+501T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 7/29 | chr20 | 38516871 | ||||||
| chr20:38516932
|
T | C | 4 | a0001c0001t0001g0034a0001c0001t0001g0144a0001c0001t0001g0170others(1): Show | 4 | HG02015.hp2 NA18981.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.1051+562T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 7/29 | chr20 | 38516932 | ||||||
| chr20:38517013
|
T | C | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1052-493T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 7/29 | chr20 | 38517013 | ||||||
| chr20:38517319
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1052-187C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 7/29 | chr20 | 38517319 | ||||||
| chr20:38517732
|
A | G | 35 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(32): Show | 38 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(35): Show |
intron_variant | MODIFIER | c.1201-52A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 8/29 | chr20 | 38517732 | ||||||
| chr20:38518123
|
A | G | 1 | a0001c0001t0002g0152 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1417+123A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38518123 | ||||||
| chr20:38518375
|
G | A | 14 | a0001c0002t0002g0122a0001c0002t0002g0123a0001c0002t0002g0124others(11): Show | 15 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.1417+375G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38518375 | ||||||
| chr20:38518402
|
A | G | 5 | a0001c0001t0001g0041a0001c0001t0001g0135a0001c0001t0001g0136others(2): Show | 5 | HG00741.hp2 HG02280.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.1417+402A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38518402 | ||||||
| chr20:38518404
|
A | G | 8 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0003g0197others(5): Show | 9 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1417+404A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38518404 | ||||||
| chr20:38518514
|
CTT | C | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0003g0197 | 3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1417+515_1417+516d others(4): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38518514 | ||||||
| chr20:38518750
|
T | G | 1 | a0001c0001t0004g0028 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1417+750T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38518750 | ||||||
| chr20:38518958
|
C | G | 12 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(9): Show | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1417+958C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38518958 | ||||||
| chr20:38519024
|
A | G | 12 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(9): Show | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1417+1024A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38519024 | ||||||
| chr20:38519076
|
A | G | 4 | a0001c0001t0003g0035a0001c0001t0003g0036a0001c0001t0003g0038others(1): Show | 4 | HG01071.hp2 HG01081.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.1417+1076A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38519076 | ||||||
| chr20:38519296
|
C | T | 6 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0012others(3): Show | 6 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1417+1296C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38519296 | ||||||
| chr20:38519452
|
A | T | 1 | a0001c0001t0001g0073 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1417+1452A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38519452 | ||||||
| chr20:38519505
|
T | C | 3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1417+1505T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38519505 | ||||||
| chr20:38519588
|
A | C | 20 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(17): Show | 21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1417+1588A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38519588 | ||||||
| chr20:38520372
|
T | A | 20 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(17): Show | 21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1418-1125T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38520372 | ||||||
| chr20:38520524
|
C | CT | 37 | a0001c0001t0001g0146a0001c0001t0001g0198a0001c0001t0001g0199others(34): Show | 40 | HG01109.hp1 HG01109.hp2 HG01884.hp2 others(37): Show |
intron_variant | MODIFIER | c.1418-951dupT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr20 | 38520524 | |||||
| chr20:38520524
|
C | CTT | 16 | a0001c0001t0001g0041a0001c0001t0001g0135a0001c0001t0001g0136others(13): Show | 17 | HG00642.hp1 HG00741.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1418-952_1418-951d others(4): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr20 | 38520524 | |||||
| chr20:38520524
|
C | CTTT | 12 | a0001c0001t0004g0019a0001c0002t0002g0122a0001c0002t0002g0123others(9): Show | 13 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.1418-953_1418-951d others(5): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr20 | 38520524 | |||||
| chr20:38520524
|
CT | C | 8 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0114others(5): Show | 8 | HG01168.hp2 HG02896.hp1 HG03239.hp2 others(5): Show |
intron_variant | MODIFIER | c.1418-951delT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr20 | 38520524 | |||||
| chr20:38521066
|
A | G | 1 | a0001c0001t0003g0192 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1418-431A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38521066 | ||||||
| chr20:38521396
|
T | C | 1 | a0001c0001t0001g0102 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1418-101T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 9/29 | chr20 | 38521396 | ||||||
| chr20:38521922
|
G | C | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0003g0197 | 3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1619+224G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38521922 | ||||||
| chr20:38521995
|
T | C | 1 | a0001c0001t0001g0100 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1619+297T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38521995 | ||||||
| chr20:38522075
|
G | A | 35 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(32): Show | 38 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(35): Show |
intron_variant | MODIFIER | c.1619+377G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38522075 | ||||||
| chr20:38522166
|
C | T | 1 | a0001c0003t0010g0202 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1619+468C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38522166 | ||||||
| chr20:38522192
|
C | T | 3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1619+494C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38522192 | ||||||
| chr20:38522193
|
A | G | 36 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(33): Show | 39 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(36): Show |
intron_variant | MODIFIER | c.1619+495A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38522193 | ||||||
| chr20:38522198
|
A | G | 1 | a0001c0001t0004g0024 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1619+500A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38522198 | ||||||
| chr20:38522387
|
A | G | 3 | a0001c0002t0002g0130a0001c0002t0002g0131a0001c0002t0002g0132 | 3 | HG02809.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1619+689A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38522387 | ||||||
| chr20:38522531
|
C | T | 1 | a0001c0001t0027g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1619+833C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38522531 | ||||||
| chr20:38522955
|
T | C | 5 | a0001c0001t0002g0147a0001c0001t0002g0165a0001c0001t0002g0166others(2): Show | 5 | HG01109.hp2 HG01978.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1619+1257T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38522955 | ||||||
| chr20:38523153
|
CA | C | 7 | a0001c0001t0006g0002a0001c0001t0006g0029a0001c0001t0006g0030others(4): Show | 8 | HG01884.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1619+1469delA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr20 | 38523153 | |||||
| chr20:38523246
|
G | C | 84 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(81): Show | 85 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.1620-1532G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38523246 | ||||||
| chr20:38523362
|
A | G | 1 | a0001c0001t0002g0152 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1620-1416A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38523362 | ||||||
| chr20:38524277
|
A | C | 20 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(17): Show | 21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1620-501A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38524277 | ||||||
| chr20:38524400
|
G | A | 36 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(33): Show | 39 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(36): Show |
intron_variant | MODIFIER | c.1620-378G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38524400 | ||||||
| chr20:38524491
|
AT | A | 88 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(85): Show | 89 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.1620-276delT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr20 | 38524491 | |||||
| chr20:38524642
|
T | C | 1 | a0001c0001t0001g0074 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1620-136T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38524642 | ||||||
| chr20:38524647
|
A | G | 1 | a0001c0001t0025g0097 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1620-131A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38524647 | ||||||
| chr20:38524745
|
A | T | 20 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(17): Show | 21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1620-33A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 10/29 | chr20 | 38524745 | ||||||
| chr20:38525583
|
C | T | 5 | a0001c0001t0006g0002a0001c0001t0006g0029a0001c0001t0006g0030others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1902+65C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 12/29 | chr20 | 38525583 | ||||||
| chr20:38525656
|
A | C | 1 | a0001c0001t0003g0079 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1902+138A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 12/29 | chr20 | 38525656 | ||||||
| chr20:38525802
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1903-93C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 12/29 | chr20 | 38525802 | ||||||
| chr20:38526247
|
C | A | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2050+205C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38526247 | ||||||
| chr20:38526592
|
T | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0106 | 2 | HG00639.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2050+550T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38526592 | ||||||
| chr20:38526906
|
G | A | 6 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0012others(3): Show | 6 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2050+864G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38526906 | ||||||
| chr20:38527125
|
C | G | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137 | 3 | HG00741.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2050+1083C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38527125 | ||||||
| chr20:38527265
|
G | C | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2050+1223G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38527265 | ||||||
| chr20:38527294
|
A | G | 1 | a0001c0001t0027g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2050+1252A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38527294 | ||||||
| chr20:38527317
|
G | C | 6 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0012others(3): Show | 6 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2050+1275G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38527317 | ||||||
| chr20:38527379
|
T | A | 1 | a0001c0001t0003g0094 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2050+1337T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38527379 | ||||||
| chr20:38527491
|
C | G | 1 | a0001c0001t0027g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2050+1449C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38527491 | ||||||
| chr20:38527502
|
T | A | 1 | a0001c0001t0001g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2050+1460T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38527502 | ||||||
| chr20:38527510
|
T | C | 1 | a0001c0001t0004g0024 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2050+1468T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38527510 | ||||||
| chr20:38527644
|
G | A | 14 | a0001c0002t0002g0122a0001c0002t0002g0123a0001c0002t0002g0124others(11): Show | 15 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.2050+1602G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38527644 | ||||||
| chr20:38527725
|
G | A | 6 | a0001c0001t0001g0063a0001c0001t0001g0106a0001c0001t0003g0107others(3): Show | 6 | HG00639.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2050+1683G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38527725 | ||||||
| chr20:38527855
|
G | A | 3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2050+1813G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38527855 | ||||||
| chr20:38528232
|
A | G | 35 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(32): Show | 38 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(35): Show |
intron_variant | MODIFIER | c.2050+2190A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38528232 | ||||||
| chr20:38528333
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2050+2291C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38528333 | ||||||
| chr20:38528345
|
T | A | 1 | a0001c0002t0002g0126 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2050+2303T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38528345 | ||||||
| chr20:38528345
|
T | TTTTA | 9 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(6): Show | 9 | HG00741.hp2 HG02280.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.2050+2344_2050+234 others(8): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr20 | 38528345 | |||||
| chr20:38528345
|
T | TTTTATTT others(1): Show |
5 | a0001c0001t0001g0199a0001c0002t0002g0124a0001c0002t0002g0125others(2): Show | 5 | HG01243.hp2 HG02145.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2050+2340_2050+234 others(12): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr20 | 38528345 | |||||
| chr20:38528345
|
TTTTA | T | 16 | a0001c0001t0001g0034a0001c0001t0001g0140a0001c0001t0001g0144others(13): Show | 16 | HG01256.hp1 HG01993.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.2050+2344_2050+234 others(8): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr20 | 38528345 | |||||
| chr20:38528345
|
TTTTATTT others(1): Show |
T | 63 | a0001c0001t0001g0169a0001c0001t0001g0183a0001c0001t0001g0184others(60): Show | 65 | HG00280.hp2 HG00642.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.2050+2340_2050+234 others(12): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr20 | 38528345 | |||||
| chr20:38528345
|
TTTTATTT others(5): Show |
T | 98 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(95): Show | 100 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.2050+2336_2050+234 others(16): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr20 | 38528345 | |||||
| chr20:38528345
|
TTTTATTT others(17): Show |
T | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG03239.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.2050+2324_2050+234 others(28): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr20 | 38528345 | |||||
| chr20:38528357
|
A | T | 1 | a0001c0001t0003g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2050+2315A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38528357 | ||||||
| chr20:38528396
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2050+2354A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38528396 | ||||||
| chr20:38528613
|
C | T | 8 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0003g0197others(5): Show | 9 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2051-2554C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38528613 | ||||||
| chr20:38528711
|
C | T | 9 | a0001c0001t0001g0062a0001c0001t0001g0103a0001c0001t0009g0010others(6): Show | 9 | HG01361.hp1 HG02145.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2051-2456C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38528711 | ||||||
| chr20:38528723
|
C | G | 1 | a0001c0001t0002g0120 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2051-2444C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38528723 | ||||||
| chr20:38528740
|
G | A | 1 | a0001c0001t0027g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2051-2427G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38528740 | ||||||
| chr20:38528827
|
C | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 4 | HG00741.hp2 HG02280.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2051-2340C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38528827 | ||||||
| chr20:38528853
|
G | A | 7 | a0001c0001t0006g0016a0001c0001t0009g0010a0001c0001t0009g0011others(4): Show | 7 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2051-2314G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38528853 | ||||||
| chr20:38528912
|
T | C | 20 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(17): Show | 21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.2051-2255T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38528912 | ||||||
| chr20:38528972
|
G | A | 1 | a0001c0008t0001g0049 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2051-2195G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38528972 | ||||||
| chr20:38529170
|
A | G | 1 | a0001c0001t0001g0065 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2051-1997A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38529170 | ||||||
| chr20:38529203
|
A | G | 1 | a0001c0001t0001g0191 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2051-1964A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38529203 | ||||||
| chr20:38529310
|
A | G | 151 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(148): Show | 157 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.2051-1857A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38529310 | ||||||
| chr20:38529517
|
C | CA | 7 | a0001c0001t0001g0065a0001c0001t0001g0116a0001c0001t0001g0139others(4): Show | 7 | HG01106.hp2 HG02071.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.2051-1638dupA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr20 | 38529517 | |||||
| chr20:38529525
|
A | T | 1 | a0001c0001t0003g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2051-1642A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38529525 | ||||||
| chr20:38529530
|
T | A | 1 | a0001c0001t0027g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2051-1637T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38529530 | ||||||
| chr20:38529565
|
G | T | 1 | a0001c0001t0001g0080 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2051-1602G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38529565 | ||||||
| chr20:38529613
|
A | C | 2 | a0001c0001t0021g0023a0001c0001t0022g0022 | 2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2051-1554A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38529613 | ||||||
| chr20:38529645
|
A | T | 1 | a0001c0001t0006g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2051-1522A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38529645 | ||||||
| chr20:38529682
|
A | G | 20 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(17): Show | 21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.2051-1485A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38529682 | ||||||
| chr20:38529701
|
G | A | 6 | a0001c0001t0001g0063a0001c0001t0001g0106a0001c0001t0003g0107others(3): Show | 6 | HG00639.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2051-1466G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38529701 | ||||||
| chr20:38529715
|
C | T | 20 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(17): Show | 21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.2051-1452C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38529715 | ||||||
| chr20:38529743
|
G | A | 5 | a0001c0001t0006g0002a0001c0001t0006g0029a0001c0001t0006g0030others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2051-1424G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38529743 | ||||||
| chr20:38529791
|
A | G | 5 | a0001c0001t0006g0002a0001c0001t0006g0029a0001c0001t0006g0030others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2051-1376A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38529791 | ||||||
| chr20:38530193
|
T | C | 5 | a0001c0001t0006g0002a0001c0001t0006g0029a0001c0001t0006g0030others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2051-974T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38530193 | ||||||
| chr20:38530303
|
A | C | 19 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(16): Show | 20 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.2051-864A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38530303 | ||||||
| chr20:38530339
|
A | G | 5 | a0001c0001t0006g0002a0001c0001t0006g0029a0001c0001t0006g0030others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2051-828A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38530339 | ||||||
| chr20:38530393
|
G | A | 1 | a0001c0001t0027g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2051-774G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | chr20 | 38530393 | ||||||
| chr20:38530891
|
A | AT | 86 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(83): Show | 87 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.2051-261dupT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr20 | 38530891 | |||||
| chr20:38531465
|
A | C | 3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2115+234A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 14/29 | chr20 | 38531465 | ||||||
| chr20:38531506
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2115+275A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 14/29 | chr20 | 38531506 | ||||||
| chr20:38531805
|
A | G | 41 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(38): Show | 45 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(42): Show |
intron_variant | MODIFIER | c.2115+574A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 14/29 | chr20 | 38531805 | ||||||
| chr20:38531843
|
G | A | 1 | a0001c0001t0020g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2115+612G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 14/29 | chr20 | 38531843 | ||||||
| chr20:38531878
|
C | G | 1 | a0001c0001t0001g0086 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2115+647C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 14/29 | chr20 | 38531878 | ||||||
| chr20:38531922
|
T | C | 6 | a0001c0001t0006g0002a0001c0001t0006g0016a0001c0001t0006g0029others(3): Show | 7 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2115+691T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 14/29 | chr20 | 38531922 | ||||||
| chr20:38532117
|
G | A | 11 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(8): Show | 12 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.2116-613G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 14/29 | chr20 | 38532117 | ||||||
| chr20:38532206
|
C | T | 2 | a0001c0002t0007g0004a0001c0002t0007g0134 | 3 | HG00642.hp2 HG01433.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.2116-524C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 14/29 | chr20 | 38532206 | ||||||
| chr20:38532325
|
G | A | 3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2116-405G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 14/29 | chr20 | 38532325 | ||||||
| chr20:38532363
|
A | G | 6 | a0001c0001t0006g0002a0001c0001t0006g0016a0001c0001t0006g0029others(3): Show | 7 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2116-367A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 14/29 | chr20 | 38532363 | ||||||
| chr20:38532486
|
A | G | 1 | a0001c0001t0027g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2116-244A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 14/29 | chr20 | 38532486 | ||||||
| chr20:38532974
|
A | C | 1 | a0001c0001t0017g0175 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2245+115A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38532974 | ||||||
| chr20:38533047
|
A | G | 1 | a0001c0001t0003g0197 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2245+188A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38533047 | ||||||
| chr20:38533067
|
G | A | 1 | a0001c0001t0003g0035 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2245+208G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38533067 | ||||||
| chr20:38533069
|
A | G | 1 | a0001c0001t0028g0066 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2245+210A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38533069 | ||||||
| chr20:38533165
|
C | T | 5 | a0001c0001t0001g0086a0001c0001t0001g0112a0001c0001t0003g0076others(2): Show | 5 | HG02004.hp1 HG02293.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.2245+306C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38533165 | ||||||
| chr20:38533271
|
G | A | 1 | a0001c0001t0017g0175 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2245+412G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38533271 | ||||||
| chr20:38533360
|
G | C | 35 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(32): Show | 38 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(35): Show |
intron_variant | MODIFIER | c.2245+501G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38533360 | ||||||
| chr20:38533612
|
G | A | 4 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0109others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2245+753G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38533612 | ||||||
| chr20:38533777
|
A | G | 1 | a0001c0001t0004g0024 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2245+918A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38533777 | ||||||
| chr20:38533890
|
G | C | 1 | a0004c0010t0001g0111 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2245+1031G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38533890 | ||||||
| chr20:38534138
|
C | CA | 10 | a0001c0001t0001g0040a0001c0001t0001g0060a0001c0001t0001g0080others(7): Show | 10 | HG00735.hp1 HG01255.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.2246-918dupA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr20 | 38534138 | |||||
| chr20:38534417
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2246-657T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38534417 | ||||||
| chr20:38534504
|
C | A | 1 | a0001c0001t0002g0095 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2246-570C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38534504 | ||||||
| chr20:38534724
|
A | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0144 | 2 | HG02015.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.2246-350A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38534724 | ||||||
| chr20:38534729
|
A | G | 12 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(9): Show | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2246-345A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38534729 | ||||||
| chr20:38534794
|
C | T | 7 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0186others(4): Show | 7 | NA18941.hp1 NA18956.hp1 NA18980.hp2 others(4): Show |
intron_variant | MODIFIER | c.2246-280C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38534794 | ||||||
| chr20:38534963
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2246-111C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 15/29 | chr20 | 38534963 | ||||||
| chr20:38535254
|
G | C | 1 | a0001c0001t0001g0070 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2379+47G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38535254 | ||||||
| chr20:38535356
|
C | T | 3 | a0001c0001t0002g0158a0001c0001t0002g0159a0001c0001t0002g0176 | 3 | NA18973.hp1 NA19012.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.2379+149C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38535356 | ||||||
| chr20:38535652
|
G | A | 19 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(16): Show | 20 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.2379+445G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38535652 | ||||||
| chr20:38535910
|
C | T | 3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2379+703C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38535910 | ||||||
| chr20:38536031
|
T | C | 12 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(9): Show | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2379+824T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38536031 | ||||||
| chr20:38536313
|
C | T | 1 | a0001c0001t0003g0094 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2379+1106C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38536313 | ||||||
| chr20:38536437
|
A | T | 20 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(17): Show | 21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.2379+1230A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38536437 | ||||||
| chr20:38536692
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2379+1485C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38536692 | ||||||
| chr20:38536717
|
C | G | 12 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(9): Show | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2379+1510C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38536717 | ||||||
| chr20:38536903
|
T | G | 2 | a0001c0001t0001g0139a0001c0001t0028g0066 | 2 | HG01106.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.2379+1696T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38536903 | ||||||
| chr20:38537034
|
C | T | 5 | a0001c0001t0002g0147a0001c0001t0002g0165a0001c0001t0002g0166others(2): Show | 5 | HG01109.hp2 HG01978.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.2379+1827C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38537034 | ||||||
| chr20:38537175
|
A | G | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0003g0197 | 3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2379+1968A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38537175 | ||||||
| chr20:38537176
|
T | C | 1 | a0001c0001t0001g0080 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2379+1969T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38537176 | ||||||
| chr20:38537180
|
A | G | 13 | a0001c0001t0019g0194a0001c0003t0005g0005a0001c0003t0005g0203others(10): Show | 15 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.2379+1973A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38537180 | ||||||
| chr20:38537282
|
A | G | 36 | a0001c0001t0001g0034a0001c0001t0001g0140a0001c0001t0001g0144others(33): Show | 36 | HG00738.hp2 HG02015.hp2 HG02027.hp2 others(33): Show |
intron_variant | MODIFIER | c.2379+2075A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38537282 | ||||||
| chr20:38537295
|
C | CA | 7 | a0001c0001t0003g0064a0001c0001t0006g0002a0001c0001t0006g0016others(4): Show | 8 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.2379+2096dupA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr20 | 38537295 | |||||
| chr20:38537355
|
C | G | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2379+2148C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38537355 | ||||||
| chr20:38537505
|
CAA | C | 3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2380-2270_2380-226 others(6): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38537505 | ||||||
| chr20:38537565
|
C | T | 6 | a0001c0001t0006g0002a0001c0001t0006g0016a0001c0001t0006g0029others(3): Show | 7 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2380-2211C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38537565 | ||||||
| chr20:38537683
|
A | T | 1 | a0001c0001t0002g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2380-2093A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38537683 | ||||||
| chr20:38537715
|
G | A | 147 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(144): Show | 153 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(150): Show |
intron_variant | MODIFIER | c.2380-2061G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38537715 | ||||||
| chr20:38537918
|
A | G | 1 | a0001c0001t0025g0097 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2380-1858A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38537918 | ||||||
| chr20:38538009
|
T | C | 12 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(9): Show | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2380-1767T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38538009 | ||||||
| chr20:38538288
|
G | A | 4 | a0001c0001t0001g0041a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 4 | HG00741.hp2 HG02280.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2380-1488G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38538288 | ||||||
| chr20:38538331
|
G | C | 1 | a0001c0001t0004g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2380-1445G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38538331 | ||||||
| chr20:38538405
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0114a0001c0001t0001g0115 | 4 | HG00735.hp2 HG01517.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2380-1371G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38538405 | ||||||
| chr20:38538406
|
C | T | 2 | a0001c0001t0001g0198a0001c0001t0003g0197 | 2 | HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2380-1370C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38538406 | ||||||
| chr20:38538440
|
A | G | 6 | a0001c0001t0006g0002a0001c0001t0006g0016a0001c0001t0006g0029others(3): Show | 7 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2380-1336A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38538440 | ||||||
| chr20:38538500
|
G | A | 6 | a0001c0001t0006g0002a0001c0001t0006g0016a0001c0001t0006g0029others(3): Show | 7 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2380-1276G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38538500 | ||||||
| chr20:38538639
|
C | T | 1 | a0001c0001t0002g0053 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2380-1137C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38538639 | ||||||
| chr20:38539024
|
A | G | 1 | a0001c0001t0027g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2380-752A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38539024 | ||||||
| chr20:38539180
|
A | G | 1 | a0001c0001t0001g0065 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2380-596A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38539180 | ||||||
| chr20:38539378
|
T | C | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137 | 3 | HG00741.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2380-398T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38539378 | ||||||
| chr20:38539611
|
C | T | 6 | a0001c0001t0001g0065a0001c0001t0001g0116a0001c0001t0001g0138others(3): Show | 6 | HG01106.hp2 HG02056.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.2380-165C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38539611 | ||||||
| chr20:38539616
|
C | T | 2 | a0001c0001t0002g0161a0001c0001t0002g0162 | 2 | NA18974.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2380-160C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 16/29 | chr20 | 38539616 | ||||||
| chr20:38540291
|
G | C | 14 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(11): Show | 14 | NA18941.hp1 NA18949.hp1 NA18956.hp1 others(11): Show |
intron_variant | MODIFIER | c.2562+333G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 17/29 | chr20 | 38540291 | ||||||
| chr20:38540749
|
A | T | 205 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0037others(202): Show | 211 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(208): Show |
intron_variant | MODIFIER | c.2563-292A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 17/29 | chr20 | 38540749 | ||||||
| chr20:38541011
|
T | C | 54 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(51): Show | 59 | HG00642.hp1 HG00642.hp2 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.2563-30T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 17/29 | chr20 | 38541011 | ||||||
| chr20:38541335
|
G | A | 1 | a0001c0001t0027g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2714+143G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38541335 | ||||||
| chr20:38541349
|
A | G | 1 | a0001c0001t0003g0076 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2714+157A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38541349 | ||||||
| chr20:38542491
|
TA | T | 12 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(9): Show | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2714+1308delA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr20 | 38542491 | |||||
| chr20:38542622
|
A | G | 36 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(33): Show | 39 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(36): Show |
intron_variant | MODIFIER | c.2714+1430A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38542622 | ||||||
| chr20:38542649
|
G | A | 5 | a0001c0001t0006g0002a0001c0001t0006g0029a0001c0001t0006g0030others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2714+1457G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38542649 | ||||||
| chr20:38542704
|
A | G | 36 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(33): Show | 39 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(36): Show |
intron_variant | MODIFIER | c.2714+1512A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38542704 | ||||||
| chr20:38542780
|
C | T | 1 | a0001c0001t0007g0163 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2714+1588C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38542780 | ||||||
| chr20:38542798
|
C | T | 1 | a0001c0001t0027g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2714+1606C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38542798 | ||||||
| chr20:38542814
|
G | T | 1 | a0001c0008t0001g0049 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2714+1622G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38542814 | ||||||
| chr20:38542843
|
A | G | 21 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(18): Show | 22 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.2714+1651A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38542843 | ||||||
| chr20:38542865
|
G | GA | 15 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(12): Show | 17 | HG01109.hp1 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.2714+1683dupA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr20 | 38542865 | |||||
| chr20:38543468
|
C | A | 1 | a0001c0001t0003g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2714+2276C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38543468 | ||||||
| chr20:38543473
|
T | C | 4 | a0001c0001t0004g0024a0001c0001t0004g0025a0001c0001t0004g0027others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2714+2281T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38543473 | ||||||
| chr20:38543765
|
A | G | 2 | a0001c0001t0002g0161a0001c0001t0002g0162 | 2 | NA18974.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2715-2478A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38543765 | ||||||
| chr20:38544014
|
C | T | 1 | a0001c0001t0024g0015 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2715-2229C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38544014 | ||||||
| chr20:38544171
|
C | T | 4 | a0001c0001t0004g0024a0001c0001t0004g0025a0001c0001t0004g0027others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2715-2072C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38544171 | ||||||
| chr20:38544178
|
A | C | 3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2715-2065A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38544178 | ||||||
| chr20:38544232
|
C | T | 1 | a0001c0002t0002g0123 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2715-2011C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38544232 | ||||||
| chr20:38544745
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2715-1498G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38544745 | ||||||
| chr20:38544843
|
G | A | 38 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(35): Show | 39 | HG00558.hp2 HG00639.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.2715-1400G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38544843 | ||||||
| chr20:38545181
|
A | G | 1 | a0001c0001t0020g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2715-1062A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38545181 | ||||||
| chr20:38545245
|
A | T | 1 | a0001c0001t0001g0189 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2715-998A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38545245 | ||||||
| chr20:38545512
|
A | G | 1 | a0001c0001t0003g0048 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2715-731A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38545512 | ||||||
| chr20:38545545
|
A | C | 1 | a0001c0001t0001g0169 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2715-698A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38545545 | ||||||
| chr20:38545551
|
C | T | 1 | a0001c0001t0004g0018 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2715-692C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38545551 | ||||||
| chr20:38545673
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2715-570G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38545673 | ||||||
| chr20:38545761
|
A | G | 4 | a0001c0001t0004g0024a0001c0001t0004g0025a0001c0001t0004g0027others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2715-482A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38545761 | ||||||
| chr20:38545917
|
G | C | 7 | a0001c0001t0003g0035a0001c0001t0003g0036a0001c0001t0003g0038others(4): Show | 7 | HG00280.hp1 HG01071.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.2715-326G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38545917 | ||||||
| chr20:38545944
|
A | G | 2 | a0001c0001t0002g0142a0001c0001t0002g0143 | 2 | HG00280.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.2715-299A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | chr20 | 38545944 | ||||||
| chr20:38546070
|
G | GA | 6 | a0001c0001t0006g0002a0001c0001t0006g0016a0001c0001t0006g0029others(3): Show | 7 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2715-172dupA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr20 | 38546070 | |||||
| chr20:38546526
|
T | A | 1 | a0001c0001t0020g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2902+96T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38546526 | ||||||
| chr20:38546536
|
G | A | 2 | a0001c0001t0008g0171a0001c0001t0008g0172 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2902+106G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38546536 | ||||||
| chr20:38546599
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2902+169T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38546599 | ||||||
| chr20:38546611
|
A | G | 7 | a0001c0001t0006g0002a0001c0001t0006g0016a0001c0001t0006g0029others(4): Show | 8 | HG01884.hp2 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2902+181A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38546611 | ||||||
| chr20:38546708
|
G | T | 13 | a0001c0001t0004g0024a0001c0001t0004g0025a0001c0001t0004g0027others(10): Show | 13 | HG01361.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2902+278G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38546708 | ||||||
| chr20:38546779
|
G | A | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0003g0197 | 3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2902+349G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38546779 | ||||||
| chr20:38546838
|
C | G | 19 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(16): Show | 20 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.2902+408C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38546838 | ||||||
| chr20:38546873
|
A | G | 12 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(9): Show | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2902+443A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38546873 | ||||||
| chr20:38547007
|
C | G | 1 | a0001c0001t0002g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2902+577C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38547007 | ||||||
| chr20:38547847
|
C | T | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2903-842C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38547847 | ||||||
| chr20:38547888
|
A | G | 1 | a0001c0001t0001g0102 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2903-801A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38547888 | ||||||
| chr20:38547916
|
G | C | 1 | a0001c0001t0003g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2903-773G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38547916 | ||||||
| chr20:38548053
|
G | T | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0003g0197 | 3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2903-636G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38548053 | ||||||
| chr20:38548076
|
C | T | 2 | a0001c0003t0005g0005a0001c0003t0005g0208 | 3 | HG02451.hp1 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2903-613C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38548076 | ||||||
| chr20:38548136
|
TCCATCCT others(17): Show |
T | 1 | a0001c0001t0001g0138 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2903-550_2903-527d others(26): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr20 | 38548136 | |||||
| chr20:38548366
|
G | A | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2903-323G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38548366 | ||||||
| chr20:38548384
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2903-305G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38548384 | ||||||
| chr20:38548532
|
T | C | 37 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(34): Show | 41 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(38): Show |
intron_variant | MODIFIER | c.2903-157T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 19/29 | chr20 | 38548532 | ||||||
| chr20:38548984
|
G | C | 39 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(36): Show | 40 | HG00558.hp2 HG00639.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.3009+189G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38548984 | ||||||
| chr20:38549288
|
T | C | 12 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(9): Show | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.3009+493T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38549288 | ||||||
| chr20:38549295
|
A | C | 1 | a0001c0001t0007g0163 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3009+500A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38549295 | ||||||
| chr20:38549533
|
TA | T | 9 | a0001c0001t0001g0056a0001c0001t0001g0065a0001c0001t0001g0099others(6): Show | 9 | HG01069.hp1 HG02622.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.3009+755delA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 38549533 | |||||
| chr20:38549543
|
A | T | 4 | a0001c0001t0006g0002a0001c0002t0002g0124a0001c0002t0007g0004others(1): Show | 6 | HG00642.hp2 HG01433.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.3009+748A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38549543 | ||||||
| chr20:38549545
|
A | T | 25 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(22): Show | 28 | HG00642.hp2 HG00741.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.3009+750A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38549545 | ||||||
| chr20:38549547
|
A | AT | 5 | a0001c0001t0002g0147a0001c0001t0002g0159a0001c0001t0002g0176others(2): Show | 5 | HG01978.hp1 HG02109.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.3009+752_3009+753i others(3): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38549547 | ||||||
| chr20:38549547
|
A | T | 53 | a0001c0001t0001g0041a0001c0001t0001g0063a0001c0001t0001g0089others(50): Show | 57 | HG00639.hp2 HG00642.hp2 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.3009+752A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38549547 | ||||||
| chr20:38549549
|
A | AT | 4 | a0001c0001t0001g0042a0001c0001t0001g0084a0001c0001t0002g0158others(1): Show | 4 | HG03486.hp1 NA18973.hp1 NA19091.hp1 others(1): Show |
intron_variant | MODIFIER | c.3009+754_3009+755i others(3): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38549549 | ||||||
| chr20:38549549
|
A | T | 162 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0041others(159): Show | 168 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(165): Show |
intron_variant | MODIFIER | c.3009+754A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38549549 | ||||||
| chr20:38549551
|
T | A | 1 | a0001c0001t0003g0059 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3009+756T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38549551 | ||||||
| chr20:38549563
|
T | C | 3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3009+768T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38549563 | ||||||
| chr20:38549563
|
T | TATAC | 7 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(4): Show | 8 | HG02451.hp1 HG02922.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.3009+769_3009+770i others(6): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 38549563 | |||||
| chr20:38549575
|
CACAT | C | 10 | a0001c0002t0002g0122a0001c0002t0002g0123a0001c0002t0002g0124others(7): Show | 10 | HG02145.hp2 HG02258.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.3009+786_3009+789d others(6): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 38549575 | |||||
| chr20:38549585
|
T | TAC | 2 | a0001c0001t0027g0121a0003c0006t0003g0033 | 2 | HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.3009+806_3009+807d others(4): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 38549585 | |||||
| chr20:38549585
|
TAC | T | 82 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(79): Show | 83 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.3009+806_3009+807d others(4): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 38549585 | |||||
| chr20:38549585
|
TACAC | T | 4 | a0001c0001t0001g0116a0001c0001t0001g0144a0001c0005t0001g0117others(1): Show | 4 | NA19001.hp1 NA19006.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.3009+804_3009+807d others(6): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 38549585 | |||||
| chr20:38549720
|
A | G | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3009+925A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38549720 | ||||||
| chr20:38549738
|
A | G | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0003g0197 | 3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.3009+943A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38549738 | ||||||
| chr20:38549785
|
C | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0099 | 2 | NA18956.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.3009+990C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38549785 | ||||||
| chr20:38549785
|
CT | C | 12 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(9): Show | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.3009+997delT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 38549785 | |||||
| chr20:38550038
|
G | A | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137 | 3 | HG00741.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3010-1033G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38550038 | ||||||
| chr20:38550142
|
T | G | 20 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(17): Show | 21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.3010-929T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38550142 | ||||||
| chr20:38550147
|
G | T | 1 | a0001c0001t0001g0051 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.3010-924G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38550147 | ||||||
| chr20:38550153
|
G | A | 20 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(17): Show | 21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.3010-918G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38550153 | ||||||
| chr20:38550312
|
A | T | 3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3010-759A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38550312 | ||||||
| chr20:38550323
|
A | T | 1 | a0001c0003t0010g0202 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3010-748A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38550323 | ||||||
| chr20:38550384
|
A | G | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3010-687A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38550384 | ||||||
| chr20:38550612
|
A | G | 3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3010-459A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38550612 | ||||||
| chr20:38550856
|
A | G | 5 | a0001c0001t0002g0148a0001c0001t0002g0150a0001c0001t0002g0152others(2): Show | 5 | HG00735.hp1 HG00738.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.3010-215A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 20/29 | chr20 | 38550856 | ||||||
| chr20:38551336
|
G | C | 2 | a0001c0001t0001g0074a0001c0001t0001g0099 | 2 | NA18956.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.3162+113G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | chr20 | 38551336 | ||||||
| chr20:38551657
|
T | A | 6 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(3): Show | 7 | HG00642.hp1 HG02572.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.3162+434T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | chr20 | 38551657 | ||||||
| chr20:38551708
|
A | T | 1 | a0001c0001t0001g0102 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3162+485A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | chr20 | 38551708 | ||||||
| chr20:38551831
|
C | T | 2 | a0001c0001t0001g0063a0001c0001t0001g0106 | 2 | HG00639.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3162+608C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | chr20 | 38551831 | ||||||
| chr20:38552140
|
A | AT | 83 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(80): Show | 84 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.3162+932dupT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr20 | 38552140 | |||||
| chr20:38552140
|
AT | A | 8 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0003g0197others(5): Show | 9 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.3162+932delT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr20 | 38552140 | |||||
| chr20:38552253
|
A | G | 86 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(83): Show | 87 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.3162+1030A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | chr20 | 38552253 | ||||||
| chr20:38552434
|
C | T | 1 | a0001c0001t0027g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3162+1211C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | chr20 | 38552434 | ||||||
| chr20:38552475
|
C | T | 1 | a0001c0001t0003g0064 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.3162+1252C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | chr20 | 38552475 | ||||||
| chr20:38552775
|
G | A | 85 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(82): Show | 86 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.3163-1092G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | chr20 | 38552775 | ||||||
| chr20:38552798
|
A | G | 8 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0003g0197others(5): Show | 9 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.3163-1069A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | chr20 | 38552798 | ||||||
| chr20:38552824
|
C | T | 1 | a0001c0003t0005g0208 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3163-1043C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | chr20 | 38552824 | ||||||
| chr20:38553264
|
A | G | 1 | a0001c0001t0027g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3163-603A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | chr20 | 38553264 | ||||||
| chr20:38553364
|
C | G | 1 | a0001c0001t0001g0105 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3163-503C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | chr20 | 38553364 | ||||||
| chr20:38553377
|
A | G | 4 | a0001c0001t0001g0041a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 4 | HG00741.hp2 HG02280.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.3163-490A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | chr20 | 38553377 | ||||||
| chr20:38553455
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3163-412A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | chr20 | 38553455 | ||||||
| chr20:38553525
|
A | G | 36 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(33): Show | 39 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(36): Show |
intron_variant | MODIFIER | c.3163-342A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | chr20 | 38553525 | ||||||
| chr20:38553777
|
C | CA | 13 | a0001c0001t0001g0144a0001c0001t0001g0153a0001c0001t0001g0154others(10): Show | 13 | HG02027.hp2 HG02257.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.3163-66dupA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr20 | 38553777 | |||||
| chr20:38553777
|
C | CAA | 69 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(66): Show | 71 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.3163-67_3163-66dup others(2): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr20 | 38553777 | |||||
| chr20:38553777
|
C | CAAA | 32 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0001g0051others(29): Show | 32 | HG00558.hp1 HG00735.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.3163-68_3163-66dup others(3): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr20 | 38553777 | |||||
| chr20:38553777
|
CA | C | 16 | a0001c0001t0001g0186a0001c0001t0002g0179a0001c0001t0004g0025others(13): Show | 17 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.3163-66delA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr20 | 38553777 | |||||
| chr20:38553777
|
CAA | C | 6 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(3): Show | 7 | HG00642.hp1 HG02572.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.3163-67_3163-66del others(2): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr20 | 38553777 | |||||
| chr20:38553777
|
CAAAAAAA others(6): Show |
C | 12 | a0001c0001t0001g0041a0001c0001t0001g0135a0001c0001t0001g0136others(9): Show | 13 | HG00741.hp2 HG01884.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.3163-78_3163-66del others(13): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr20 | 38553777 | |||||
| chr20:38554169
|
T | TA | 26 | a0001c0001t0001g0144a0001c0001t0003g0182a0001c0001t0004g0001others(23): Show | 27 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.3372+107dupA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | INFO_REALIGN_3_PRIME | chr20 | 38554169 | |||||
| chr20:38554169
|
TA | T | 14 | a0001c0002t0002g0122a0001c0002t0002g0123a0001c0002t0002g0124others(11): Show | 15 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.3372+107delA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | INFO_REALIGN_3_PRIME | chr20 | 38554169 | |||||
| chr20:38554181
|
A | G | 1 | a0001c0001t0002g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3372+105A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38554181 | ||||||
| chr20:38554736
|
C | T | 3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3372+660C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38554736 | ||||||
| chr20:38554742
|
A | T | 12 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(9): Show | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.3372+666A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38554742 | ||||||
| chr20:38554961
|
A | G | 1 | a0005c0011t0002g0160 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3372+885A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38554961 | ||||||
| chr20:38555162
|
A | G | 1 | a0001c0001t0002g0156 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.3372+1086A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38555162 | ||||||
| chr20:38555462
|
G | A | 1 | a0001c0001t0027g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3372+1386G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38555462 | ||||||
| chr20:38555489
|
T | C | 2 | a0001c0001t0001g0083a0001c0001t0014g0087 | 2 | HG02056.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.3372+1413T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38555489 | ||||||
| chr20:38555549
|
C | G | 12 | a0001c0001t0001g0041a0001c0001t0001g0135a0001c0001t0001g0136others(9): Show | 13 | HG00741.hp2 HG01884.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.3372+1473C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38555549 | ||||||
| chr20:38556015
|
G | A | 3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3372+1939G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38556015 | ||||||
| chr20:38556125
|
A | T | 1 | a0001c0001t0003g0107 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3372+2049A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38556125 | ||||||
| chr20:38556247
|
T | G | 4 | a0001c0001t0003g0035a0001c0001t0003g0036a0001c0001t0003g0038others(1): Show | 4 | HG01071.hp2 HG01081.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.3373-2048T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38556247 | ||||||
| chr20:38556322
|
C | T | 8 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0003g0197others(5): Show | 9 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.3373-1973C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38556322 | ||||||
| chr20:38556323
|
G | T | 2 | a0001c0001t0001g0116a0001c0005t0001g0117 | 2 | NA19006.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.3373-1972G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38556323 | ||||||
| chr20:38556327
|
A | G | 8 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0003g0197others(5): Show | 9 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.3373-1968A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38556327 | ||||||
| chr20:38556434
|
A | G | 1 | a0001c0001t0027g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3373-1861A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38556434 | ||||||
| chr20:38556783
|
A | G | 14 | a0001c0002t0002g0122a0001c0002t0002g0123a0001c0002t0002g0124others(11): Show | 15 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.3373-1512A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38556783 | ||||||
| chr20:38556965
|
A | T | 8 | a0001c0001t0002g0147a0001c0001t0002g0161a0001c0001t0002g0162others(5): Show | 8 | HG01109.hp2 HG01978.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.3373-1330A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38556965 | ||||||
| chr20:38557155
|
G | T | 1 | a0001c0001t0003g0197 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3373-1140G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38557155 | ||||||
| chr20:38557199
|
T | G | 1 | a0001c0001t0001g0051 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.3373-1096T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38557199 | ||||||
| chr20:38557224
|
A | G | 2 | a0001c0001t0001g0190a0001c0001t0003g0192 | 2 | NA18956.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3373-1071A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38557224 | ||||||
| chr20:38557342
|
A | T | 2 | a0001c0002t0007g0004a0001c0002t0007g0134 | 3 | HG00642.hp2 HG01433.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.3373-953A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38557342 | ||||||
| chr20:38557366
|
C | A | 137 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(134): Show | 143 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.3373-929C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38557366 | ||||||
| chr20:38557508
|
A | T | 12 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(9): Show | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.3373-787A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38557508 | ||||||
| chr20:38557667
|
G | T | 1 | a0001c0003t0005g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3373-628G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38557667 | ||||||
| chr20:38557674
|
C | A | 1 | a0001c0001t0023g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3373-621C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38557674 | ||||||
| chr20:38557809
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.3373-486C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38557809 | ||||||
| chr20:38557887
|
A | G | 2 | a0001c0001t0001g0055a0001c0001t0001g0071 | 2 | NA18974.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.3373-408A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38557887 | ||||||
| chr20:38557991
|
G | T | 19 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(16): Show | 20 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.3373-304G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38557991 | ||||||
| chr20:38558172
|
T | C | 2 | a0001c0001t0001g0112a0004c0010t0001g0111 | 2 | HG02004.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.3373-123T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 22/29 | chr20 | 38558172 | ||||||
| chr20:38558467
|
A | AT | 5 | a0001c0001t0001g0060a0001c0001t0003g0058a0001c0001t0003g0059others(2): Show | 5 | HG00280.hp1 HG00738.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.3531+26dupT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr20 | 38558467 | |||||
| chr20:38558573
|
G | T | 2 | a0001c0001t0001g0112a0004c0010t0001g0111 | 2 | HG02004.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.3531+120G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38558573 | ||||||
| chr20:38558989
|
G | C | 1 | a0001c0001t0001g0041 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3531+536G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38558989 | ||||||
| chr20:38559042
|
T | C | 1 | a0001c0001t0001g0086 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3531+589T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38559042 | ||||||
| chr20:38559460
|
C | T | 1 | a0001c0001t0003g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3531+1007C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38559460 | ||||||
| chr20:38559641
|
C | A | 2 | a0001c0001t0001g0112a0004c0010t0001g0111 | 2 | HG02004.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.3531+1188C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38559641 | ||||||
| chr20:38559672
|
C | T | 12 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(9): Show | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.3531+1219C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38559672 | ||||||
| chr20:38559911
|
G | T | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0003g0197 | 3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.3531+1458G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38559911 | ||||||
| chr20:38560106
|
G | GT | 17 | a0001c0002t0002g0122a0001c0002t0002g0123a0001c0002t0002g0124others(14): Show | 18 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.3531+1665dupT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr20 | 38560106 | |||||
| chr20:38560106
|
GT | G | 19 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(16): Show | 20 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.3531+1665delT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr20 | 38560106 | |||||
| chr20:38560123
|
T | C | 6 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(3): Show | 7 | HG00642.hp1 HG02572.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.3531+1670T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38560123 | ||||||
| chr20:38560235
|
T | C | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3531+1782T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38560235 | ||||||
| chr20:38560270
|
T | C | 7 | a0001c0001t0006g0016a0001c0001t0009g0010a0001c0001t0009g0011others(4): Show | 7 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.3531+1817T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38560270 | ||||||
| chr20:38560484
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.3531+2031G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38560484 | ||||||
| chr20:38560524
|
G | A | 1 | a0001c0001t0003g0192 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3532-2008G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38560524 | ||||||
| chr20:38561257
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3532-1275G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38561257 | ||||||
| chr20:38561569
|
TAGA | T | 2 | a0001c0001t0002g0142a0001c0001t0002g0143 | 2 | HG00280.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.3532-960_3532-958d others(5): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr20 | 38561569 | |||||
| chr20:38561585
|
G | A | 2 | a0001c0001t0021g0023a0001c0001t0022g0022 | 2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3532-947G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38561585 | ||||||
| chr20:38561751
|
C | A | 1 | a0001c0003t0010g0202 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3532-781C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38561751 | ||||||
| chr20:38561759
|
C | T | 19 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(16): Show | 20 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.3532-773C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38561759 | ||||||
| chr20:38561875
|
T | C | 1 | a0001c0001t0001g0085 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.3532-657T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38561875 | ||||||
| chr20:38561983
|
A | C | 14 | a0001c0002t0002g0122a0001c0002t0002g0123a0001c0002t0002g0124others(11): Show | 15 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.3532-549A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38561983 | ||||||
| chr20:38561985
|
G | A | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3532-547G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38561985 | ||||||
| chr20:38562071
|
C | T | 6 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0012others(3): Show | 6 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.3532-461C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38562071 | ||||||
| chr20:38562269
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0047 | 2 | HG00741.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.3532-263C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 23/29 | chr20 | 38562269 | ||||||
| chr20:38562748
|
GT | G | 6 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(3): Show | 7 | HG00642.hp1 HG02572.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.3697+62delT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr20 | 38562748 | |||||
| chr20:38562759
|
T | C | 5 | a0001c0001t0006g0002a0001c0001t0006g0029a0001c0001t0006g0030others(2): Show | 6 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.3697+62T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38562759 | ||||||
| chr20:38562812
|
A | G | 33 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(30): Show | 36 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(33): Show |
intron_variant | MODIFIER | c.3697+115A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38562812 | ||||||
| chr20:38563017
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3697+320A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38563017 | ||||||
| chr20:38563135
|
G | A | 20 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(17): Show | 21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.3697+438G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38563135 | ||||||
| chr20:38563144
|
T | G | 32 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(29): Show | 35 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(32): Show |
intron_variant | MODIFIER | c.3697+447T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38563144 | ||||||
| chr20:38563194
|
T | C | 3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3697+497T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38563194 | ||||||
| chr20:38563267
|
C | T | 32 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(29): Show | 35 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(32): Show |
intron_variant | MODIFIER | c.3697+570C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38563267 | ||||||
| chr20:38563357
|
A | G | 6 | a0001c0001t0006g0002a0001c0001t0006g0016a0001c0001t0006g0029others(3): Show | 7 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3697+660A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38563357 | ||||||
| chr20:38563447
|
A | G | 3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3697+750A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38563447 | ||||||
| chr20:38563848
|
C | T | 2 | a0001c0002t0007g0004a0001c0002t0007g0134 | 3 | HG00642.hp2 HG01433.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.3697+1151C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38563848 | ||||||
| chr20:38563867
|
C | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 4 | HG00741.hp2 HG02280.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.3697+1170C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38563867 | ||||||
| chr20:38563965
|
A | C | 3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3697+1268A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38563965 | ||||||
| chr20:38564175
|
A | G | 40 | a0001c0001t0001g0041a0001c0001t0001g0135a0001c0001t0001g0136others(37): Show | 43 | HG00642.hp1 HG00741.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.3698-1184A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38564175 | ||||||
| chr20:38564190
|
C | A | 1 | a0001c0001t0004g0024 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3698-1169C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38564190 | ||||||
| chr20:38564234
|
G | A | 20 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(17): Show | 21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.3698-1125G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38564234 | ||||||
| chr20:38564395
|
ACCTCTTG others(9): Show |
A | 1 | a0001c0001t0001g0081 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.3698-963_3698-948d others(18): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38564395 | ||||||
| chr20:38564412
|
T | A | 1 | a0001c0001t0001g0081 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.3698-947T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38564412 | ||||||
| chr20:38564560
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3698-799G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38564560 | ||||||
| chr20:38564686
|
C | T | 1 | a0001c0007t0003g0067 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.3698-673C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38564686 | ||||||
| chr20:38564812
|
A | AAT | 4 | a0001c0001t0001g0041a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 4 | HG00741.hp2 HG02280.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.3698-546_3698-545i others(4): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr20 | 38564812 | |||||
| chr20:38564814
|
C | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 4 | HG00741.hp2 HG02280.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.3698-545C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38564814 | ||||||
| chr20:38564877
|
C | T | 19 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(16): Show | 20 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.3698-482C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38564877 | ||||||
| chr20:38564883
|
TTCC | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0114a0001c0001t0001g0115 | 4 | HG00735.hp2 HG01517.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.3698-467_3698-465d others(5): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr20 | 38564883 | |||||
| chr20:38564961
|
G | C | 1 | a0001c0002t0002g0126 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3698-398G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38564961 | ||||||
| chr20:38564961
|
G | GTC | 3 | a0001c0001t0002g0142a0001c0001t0002g0143a0001c0003t0005g0205 | 3 | HG00280.hp2 HG02738.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3698-380_3698-379d others(4): Show |
RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr20 | 38564961 | |||||
| chr20:38565077
|
C | G | 1 | a0001c0001t0004g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3698-282C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38565077 | ||||||
| chr20:38565117
|
C | T | 2 | a0001c0001t0001g0063a0001c0001t0001g0106 | 2 | HG00639.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3698-242C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38565117 | ||||||
| chr20:38565206
|
A | G | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3698-153A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38565206 | ||||||
| chr20:38565329
|
C | A | 1 | a0001c0001t0003g0061 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3698-30C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 24/29 | chr20 | 38565329 | ||||||
| chr20:38565611
|
G | A | 84 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(81): Show | 85 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.3817+133G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 25/29 | chr20 | 38565611 | ||||||
| chr20:38565677
|
C | T | 19 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(16): Show | 20 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.3817+199C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 25/29 | chr20 | 38565677 | ||||||
| chr20:38565740
|
A | C | 1 | a0001c0003t0010g0202 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3817+262A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 25/29 | chr20 | 38565740 | ||||||
| chr20:38565790
|
C | T | 19 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(16): Show | 20 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.3817+312C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 25/29 | chr20 | 38565790 | ||||||
| chr20:38566471
|
G | T | 1 | a0001c0001t0001g0112 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3818-625G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 25/29 | chr20 | 38566471 | ||||||
| chr20:38566585
|
G | A | 1 | a0001c0001t0023g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3818-511G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 25/29 | chr20 | 38566585 | ||||||
| chr20:38566595
|
T | C | 1 | a0001c0001t0027g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3818-501T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 25/29 | chr20 | 38566595 | ||||||
| chr20:38566691
|
A | G | 12 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(9): Show | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.3818-405A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 25/29 | chr20 | 38566691 | ||||||
| chr20:38566899
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3818-197G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 25/29 | chr20 | 38566899 | ||||||
| chr20:38567001
|
G | C | 1 | a0001c0001t0001g0100 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3818-95G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 25/29 | chr20 | 38567001 | ||||||
| chr20:38567324
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3954+92A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38567324 | ||||||
| chr20:38567375
|
T | C | 20 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(17): Show | 21 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.3954+143T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38567375 | ||||||
| chr20:38567874
|
G | A | 1 | a0001c0001t0002g0147 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3954+642G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38567874 | ||||||
| chr20:38568046
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3954+814A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38568046 | ||||||
| chr20:38568262
|
CA | C | 31 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(28): Show | 34 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.3954+1040delA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr20 | 38568262 | |||||
| chr20:38568517
|
G | T | 2 | a0001c0001t0001g0037a0001c0008t0001g0049 | 2 | HG01081.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.3954+1285G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38568517 | ||||||
| chr20:38568758
|
G | A | 149 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(146): Show | 155 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(152): Show |
intron_variant | MODIFIER | c.3955-1130G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38568758 | ||||||
| chr20:38568841
|
T | G | 1 | a0001c0001t0001g0090 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3955-1047T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38568841 | ||||||
| chr20:38569024
|
T | C | 31 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(28): Show | 34 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.3955-864T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38569024 | ||||||
| chr20:38569058
|
A | C | 65 | a0001c0001t0001g0041a0001c0001t0001g0135a0001c0001t0001g0136others(62): Show | 70 | HG00642.hp1 HG00642.hp2 HG00741.hp2 others(67): Show |
intron_variant | MODIFIER | c.3955-830A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38569058 | ||||||
| chr20:38569085
|
A | G | 4 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(1): Show | 4 | HG00639.hp1 HG00741.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.3955-803A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38569085 | ||||||
| chr20:38569108
|
A | T | 1 | a0001c0001t0003g0109 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3955-780A>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38569108 | ||||||
| chr20:38569135
|
T | G | 1 | a0003c0006t0003g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3955-753T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38569135 | ||||||
| chr20:38569306
|
T | C | 19 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(16): Show | 20 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.3955-582T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38569306 | ||||||
| chr20:38569333
|
TA | T | 31 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(28): Show | 34 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.3955-553delA | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr20 | 38569333 | |||||
| chr20:38569337
|
A | G | 1 | a0001c0001t0002g0155 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3955-551A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38569337 | ||||||
| chr20:38569467
|
T | C | 3 | a0001c0001t0002g0177a0001c0001t0002g0178a0001c0001t0002g0179 | 3 | HG02257.hp1 HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3955-421T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38569467 | ||||||
| chr20:38569503
|
T | C | 1 | a0001c0001t0027g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3955-385T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38569503 | ||||||
| chr20:38569513
|
A | G | 1 | a0001c0001t0002g0158 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.3955-375A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38569513 | ||||||
| chr20:38569629
|
A | C | 6 | a0001c0001t0006g0002a0001c0001t0006g0016a0001c0001t0006g0029others(3): Show | 7 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3955-259A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38569629 | ||||||
| chr20:38569729
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3955-159C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 26/29 | chr20 | 38569729 | ||||||
| chr20:38570070
|
T | C | 2 | a0001c0001t0001g0083a0001c0001t0014g0087 | 2 | HG02056.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.4063+74T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 27/29 | chr20 | 38570070 | ||||||
| chr20:38570200
|
A | G | 11 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(8): Show | 13 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.4063+204A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 27/29 | chr20 | 38570200 | ||||||
| chr20:38570215
|
C | T | 31 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(28): Show | 34 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.4063+219C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 27/29 | chr20 | 38570215 | ||||||
| chr20:38570280
|
C | T | 6 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0012others(3): Show | 6 | HG01361.hp1 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.4063+284C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 27/29 | chr20 | 38570280 | ||||||
| chr20:38570407
|
A | G | 34 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(31): Show | 37 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(34): Show |
intron_variant | MODIFIER | c.4064-362A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 27/29 | chr20 | 38570407 | ||||||
| chr20:38570494
|
G | C | 1 | a0001c0001t0028g0066 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4064-275G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 27/29 | chr20 | 38570494 | ||||||
| chr20:38570596
|
G | A | 1 | a0001c0009t0001g0088 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.4064-173G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 27/29 | chr20 | 38570596 | ||||||
| chr20:38570637
|
A | G | 1 | a0001c0001t0027g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4064-132A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 27/29 | chr20 | 38570637 | ||||||
| chr20:38570896
|
T | C | 12 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(9): Show | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.4142+49T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38570896 | ||||||
| chr20:38571014
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.4142+167T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38571014 | ||||||
| chr20:38571418
|
C | G | 1 | a0001c0001t0002g0162 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.4142+571C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38571418 | ||||||
| chr20:38571679
|
A | G | 86 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(83): Show | 87 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.4142+832A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38571679 | ||||||
| chr20:38571891
|
T | C | 3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4142+1044T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38571891 | ||||||
| chr20:38571913
|
G | A | 1 | a0001c0001t0003g0076 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.4142+1066G>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38571913 | ||||||
| chr20:38571923
|
A | C | 12 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(9): Show | 14 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.4142+1076A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38571923 | ||||||
| chr20:38571946
|
C | T | 1 | a0001c0001t0001g0170 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.4142+1099C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38571946 | ||||||
| chr20:38571950
|
A | C | 2 | a0001c0001t0011g0013a0001c0001t0011g0014 | 2 | HG01361.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.4142+1103A>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38571950 | ||||||
| chr20:38571954
|
C | T | 192 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0037others(189): Show | 198 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(195): Show |
intron_variant | MODIFIER | c.4142+1107C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38571954 | ||||||
| chr20:38572462
|
T | C | 38 | a0001c0001t0001g0041a0001c0001t0001g0135a0001c0001t0001g0136others(35): Show | 41 | HG00642.hp1 HG00741.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.4142+1615T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38572462 | ||||||
| chr20:38572887
|
T | C | 2 | a0001c0001t0021g0023a0001c0001t0022g0022 | 2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.4143-1263T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38572887 | ||||||
| chr20:38573001
|
G | C | 3 | a0002c0004t0029g0008a0002c0004t0030g0007a0002c0004t0031g0009 | 3 | HG02258.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4143-1149G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38573001 | ||||||
| chr20:38573184
|
G | C | 1 | a0001c0001t0001g0084 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4143-966G>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38573184 | ||||||
| chr20:38573315
|
C | CT | 12 | a0001c0001t0001g0041a0001c0001t0001g0135a0001c0001t0001g0136others(9): Show | 12 | HG00741.hp2 HG01109.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.4143-824dupT | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr20 | 38573315 | |||||
| chr20:38573395
|
A | G | 1 | a0001c0002t0002g0126 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4143-755A>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38573395 | ||||||
| chr20:38573524
|
C | G | 1 | a0001c0001t0001g0119 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.4143-626C>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38573524 | ||||||
| chr20:38573530
|
T | G | 150 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0040others(147): Show | 156 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(153): Show |
intron_variant | MODIFIER | c.4143-620T>G | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38573530 | ||||||
| chr20:38573567
|
C | T | 9 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0003g0197others(6): Show | 10 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.4143-583C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38573567 | ||||||
| chr20:38573752
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.4143-398C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38573752 | ||||||
| chr20:38574132
|
C | A | 19 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(16): Show | 20 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.4143-18C>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 28/29 | chr20 | 38574132 | ||||||
| chr20:38574319
|
C | T | 19 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0018others(16): Show | 20 | HG00642.hp1 HG01361.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.4291+21C>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 29/29 | chr20 | 38574319 | ||||||
| chr20:38574447
|
T | C | 2 | a0001c0002t0007g0004a0001c0002t0007g0134 | 3 | HG00642.hp2 HG01433.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.4291+149T>C | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 29/29 | chr20 | 38574447 | ||||||
| chr20:38574597
|
G | T | 7 | a0001c0003t0005g0005a0001c0003t0005g0203a0001c0003t0005g0204others(4): Show | 8 | HG02451.hp1 HG02922.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.4292-177G>T | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 29/29 | chr20 | 38574597 | ||||||
| chr20:38574762
|
T | A | 6 | a0001c0001t0006g0002a0001c0001t0006g0016a0001c0001t0006g0029others(3): Show | 7 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.4292-12T>A | RALGAPB | ENSG00000170471.15 | transcript | ENST00000262879.11 | protein_coding | 29/29 | chr20 | 38574762 |