Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 8601 |
|---|---|
| ensemblid | ENSG00000147509.14 |
| hgncid | 14600 |
| symbol | RGS20 |
| name | regulator of G protein signaling 20 |
| refseq_nuc | NM_170587.4 |
| refseq_prot | NP_733466.1 |
| ensembl_nuc | ENST00000297313.8 |
| ensembl_prot | ENSP00000297313.3 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 53851795 |
| end | 53959303 |
| strand | + |
| ver | v1.2 |
| region | chr8:53851795-53959303 |
| region5000 | chr8:53846795-53964303 |
| regionname0 | RGS20_chr8_53851795_53959303 |
| regionname5000 | RGS20_chr8_53846795_53964303 |
| 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 | 388 | 258 | 76 | 52 | 100 | 4 | 24 | 72 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| 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 | 1167 | 242 | 61 | 51 | 100 | 4 | 24 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| c0002 | 0/0 | 1167 | 8 | 8 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| c0003 | 0/0 | 1167 | 6 | 6 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| c0004 | 0/0 | 1167 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| c0005 | 0/0 | 1167 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| 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 | 951 | 117 | 12 | 14 | 80 | 1 | 9 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| t0002 | 1/0 | 951 | 105 | 38 | 31 | 18 | 3 | 14 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| t0003 | 0/0 | 951 | 18 | 16 | 2 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| t0004 | 0/0 | 951 | 5 | 4 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| t0005 | 0/0 | 951 | 3 | 2 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| t0006 | 0/0 | 947 | 2 | 1 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| t0007 | 0/0 | 951 | 2 | 0 | 2 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| t0008 | 0/0 | 947 | 2 | 2 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| t0009 | 0/0 | 951 | 2 | 0 | 0 | 1 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| t0010 | 0/0 | 951 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| t0011 | 0/0 | 951 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| 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 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0127 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0166 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| 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 | 1167 | 242 | 61 | 51 | 100 | 4 | 24 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| a0001c0002 | 0/0 | 1167 | 8 | 8 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| a0001c0003 | 0/0 | 1167 | 6 | 6 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| a0001c0004 | 0/0 | 1167 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| a0001c0005 | 0/0 | 1167 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2117 | 115 | 10 | 14 | 80 | 1 | 9 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| a0001c0001t0002 | 1/0 | 2117 | 94 | 28 | 30 | 18 | 3 | 14 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| a0001c0001t0003 | 0/0 | 2117 | 16 | 14 | 2 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| a0001c0001t0004 | 0/0 | 2117 | 4 | 3 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| a0001c0001t0005 | 0/0 | 2117 | 3 | 2 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| a0001c0001t0006 | 0/0 | 2113 | 2 | 1 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| a0001c0001t0007 | 0/0 | 2117 | 2 | 0 | 2 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| a0001c0001t0008 | 0/0 | 2113 | 2 | 2 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| a0001c0001t0009 | 0/0 | 2117 | 2 | 0 | 0 | 1 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| a0001c0001t0010 | 0/0 | 2117 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| a0001c0001t0011 | 0/0 | 2117 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| a0001c0002t0001 | 0/0 | 2117 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| a0001c0002t0002 | 0/0 | 2117 | 6 | 6 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| a0001c0002t0003 | 0/0 | 2117 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| a0001c0003t0001 | 0/0 | 2117 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| a0001c0003t0002 | 0/0 | 2117 | 3 | 3 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| a0001c0003t0003 | 0/0 | 2117 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| a0001c0003t0004 | 0/0 | 2117 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| a0001c0004t0002 | 0/0 | 2117 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| a0001c0005t0002 | 0/0 | 2117 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | copy fasta | chr8 | 53846795 | 53964303 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0166 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0127 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0005g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0006g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0007g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0007g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0008g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0008g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0009g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0009g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0010g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0011g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0002t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0002t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0002t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0002t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0002t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0002t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0002t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0002t0003g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0003t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0003t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0003t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0003t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0003t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0003t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0004t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0005t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0220 | EUR | GBR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0150 | EUR | GBR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0162 | EUR | FIN | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0112 | EUR | FIN | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | CHS | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | CHS | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | CHS | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0228 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0258 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01069 | hp2 | a0001 | c0001 | t0006 | g0043 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01070 | hp2 | a0001 | c0001 | t0007 | g0033 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0045 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0248 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0227 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0037 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0103 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0102 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | CLM | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | CLM | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | CLM | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | CLM | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | CLM | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | CLM | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | CLM | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | CLM | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0240 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0181 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PEL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0257 | AMR | PEL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | PEL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01978 | hp2 | a0001 | c0001 | t0005 | g0221 | AMR | PEL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0185 | AMR | PEL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PEL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0118 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | KHV | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CDX | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CDX | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CDX | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CDX | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0242 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | PEL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02280 | hp2 | a0001 | c0003 | t0004 | g0027 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0239 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0109 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0044 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0245 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0151 | SAS | PJL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0170 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0244 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02809 | hp2 | a0001 | c0001 | t0008 | g0039 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02818 | hp1 | a0001 | c0003 | t0003 | g0026 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02886 | hp1 | a0001 | c0003 | t0002 | g0029 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0241 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0028 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0238 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0007 | AFR | ESN | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0179 | AFR | ESN | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02970 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | ESN | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03041 | hp1 | a0001 | c0002 | t0002 | g0009 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03041 | hp2 | a0001 | c0003 | t0002 | g0025 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0237 | AFR | MSL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | MSL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | ESN | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | ESN | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03209 | hp1 | a0001 | c0005 | t0002 | g0113 | AFR | MSL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | MSL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | MSL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03225 | hp2 | a0001 | c0002 | t0002 | g0006 | AFR | MSL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0226 | SAS | PJL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0215 | SAS | PJL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0234 | AFR | MSL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | ESN | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0233 | AFR | ESN | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0119 | AFR | MSL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0108 | AFR | MSL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0073 | SAS | PJL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0145 | SAS | PJL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | STU | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0212 | SAS | STU | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0182 | SAS | BEB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0214 | SAS | STU | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | STU | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG04184 | hp2 | a0001 | c0001 | t0009 | g0128 | SAS | BEB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | STU | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | STU | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0139 | SAS | STU | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | STU | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0114 | AFR | YRI | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | YRI | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18975 | hp2 | a0001 | c0001 | t0010 | g0188 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18993 | hp2 | a0001 | c0001 | t0009 | g0136 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19030 | hp1 | a0001 | c0002 | t0003 | g0003 | AFR | LWK | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | LWK | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | LWK | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | LWK | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | ASW | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | ASW | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0155 | SAS | GIH | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | GIH | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01123 | hp1 | a0001 | c0004 | t0002 | g0153 | AMR | CLM | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | CLM | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02109 | hp1 | a0001 | c0001 | t0011 | g0208 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02109 | hp2 | a0001 | c0003 | t0002 | g0253 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0246 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0243 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | MSL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0196 | AFR | MSL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | USA | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | USA | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | USA | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | USA | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0166 | REF | REF | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0127 | REF | REF | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:53879428
|
G | A | 1 | a0001c0003 | 6 | HG02109.hp2 HG02280.hp2 HG02818.hp1 others(3): Show |
synonymous_variant | LOW | c.336G>A | p.Pro112Pro | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/6 | 441/2117 | 336/1167 | 112/388 | chr8 | 53879428 | ||
| chr8:53879485
|
C | A | 1 | a0001c0002 | 8 | HG02559.hp1 HG02922.hp1 HG02970.hp1 others(5): Show |
synonymous_variant | LOW | c.393C>A | p.Leu131Leu | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/6 | 498/2117 | 393/1167 | 131/388 | chr8 | 53879485 | ||
| chr8:53954097
|
A | G | 1 | a0001c0005 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.765A>G | p.Glu255Glu | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/6 | 870/2117 | 765/1167 | 255/388 | chr8 | 53954097 | ||
| chr8:53958275
|
C | T | 1 | a0001c0004 | 1 | HG01123.hp1 | synonymous_variant | LOW | c.984C>T | p.Ser328Ser | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 6/6 | 1089/2117 | 984/1167 | 328/388 | chr8 | 53958275 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:53851831
|
G | A | 2 | a0001c0001t0006a0001c0001t0007 | 4 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-69G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/6 | 69 | chr8 | 53851831 | |||||
| chr8:53958503
|
C | T | 1 | a0001c0001t0005 | 3 | HG01978.hp2 HG02055.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*45C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 6/6 | 45 | chr8 | 53958503 | |||||
| chr8:53958515
|
C | T | 1 | a0001c0001t0009 | 2 | HG04184.hp2 NA18993.hp2 |
3_prime_UTR_variant | MODIFIER | c.*57C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 6/6 | 57 | chr8 | 53958515 | |||||
| chr8:53958634
|
T | C | 1 | a0001c0001t0010 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*176T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 6/6 | 176 | chr8 | 53958634 | |||||
| chr8:53958866
|
C | T | 2 | a0001c0001t0004a0001c0003t0004 | 5 | HG01167.hp1 HG02280.hp2 HG03540.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*408C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 6/6 | 408 | chr8 | 53958866 | |||||
| chr8:53958992
|
AGTAT | A | 2 | a0001c0001t0006a0001c0001t0008 | 4 | HG01069.hp2 HG02630.hp2 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*552_*555delTATG | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 6/6 | 552 | INFO_REALIGN_3_PRIME | chr8 | 53958992 | ||||
| chr8:53959019
|
A | G | 1 | a0001c0001t0011 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*561A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 6/6 | 561 | chr8 | 53959019 | |||||
| chr8:53959028
|
C | T | 3 | a0001c0001t0003a0001c0002t0003a0001c0003t0003 | 18 | HG01168.hp2 HG01169.hp2 HG01891.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*570C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 6/6 | 570 | chr8 | 53959028 | |||||
| chr8:53959197
|
A | G | 4 | a0001c0001t0001a0001c0001t0010a0001c0002t0001others(1): Show | 118 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*739A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 6/6 | 739 | chr8 | 53959197 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:53852096
|
C | T | 2 | a0001c0001t0002g0257a0001c0001t0002g0258 | 2 | HG00642.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.165+32C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53852096 | ||||||
| chr8:53852444
|
G | A | 16 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(13): Show | 16 | HG02055.hp2 HG02559.hp1 HG02895.hp2 others(13): Show |
intron_variant | MODIFIER | c.165+380G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53852444 | ||||||
| chr8:53852776
|
T | C | 16 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(13): Show | 16 | HG02055.hp2 HG02559.hp1 HG02895.hp2 others(13): Show |
intron_variant | MODIFIER | c.165+712T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53852776 | ||||||
| chr8:53852829
|
C | T | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG02818.hp2 NA19012.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.165+765C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53852829 | ||||||
| chr8:53852878
|
C | G | 2 | a0001c0001t0001g0252a0001c0003t0002g0253 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.165+814C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53852878 | ||||||
| chr8:53853496
|
T | A | 1 | a0001c0001t0002g0017 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.165+1432T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53853496 | ||||||
| chr8:53853754
|
T | C | 1 | a0001c0001t0001g0018 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.165+1690T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53853754 | ||||||
| chr8:53853981
|
G | A | 1 | a0001c0001t0002g0019 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.165+1917G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53853981 | ||||||
| chr8:53854009
|
G | A | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.165+1945G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53854009 | ||||||
| chr8:53854018
|
T | TC | 3 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0002g0251 | 3 | HG00642.hp2 HG01099.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.165+1955dupC | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53854018 | |||||
| chr8:53854208
|
G | A | 3 | a0001c0001t0001g0023a0001c0001t0003g0022a0001c0001t0003g0024 | 3 | HG02886.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.165+2144G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53854208 | ||||||
| chr8:53854287
|
G | A | 88 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(85): Show | 88 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.165+2223G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53854287 | ||||||
| chr8:53854501
|
T | C | 5 | a0001c0003t0001g0028a0001c0003t0002g0025a0001c0003t0002g0029others(2): Show | 5 | HG02280.hp2 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+2437T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53854501 | ||||||
| chr8:53854538
|
G | C | 23 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(20): Show | 23 | HG02055.hp2 HG02280.hp2 HG02559.hp1 others(20): Show |
intron_variant | MODIFIER | c.165+2474G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53854538 | ||||||
| chr8:53854559
|
A | G | 21 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(18): Show | 21 | HG02055.hp2 HG02280.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.165+2495A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53854559 | ||||||
| chr8:53854964
|
G | A | 1 | a0001c0001t0003g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.165+2900G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53854964 | ||||||
| chr8:53855016
|
A | G | 2 | a0001c0001t0002g0247a0001c0001t0002g0248 | 2 | HG01074.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.165+2952A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53855016 | ||||||
| chr8:53855135
|
G | C | 28 | a0001c0001t0001g0018a0001c0001t0001g0088a0001c0001t0001g0089others(25): Show | 28 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.165+3071G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53855135 | ||||||
| chr8:53855168
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.165+3104G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53855168 | ||||||
| chr8:53855316
|
C | T | 15 | a0001c0001t0002g0232a0001c0001t0002g0235a0001c0001t0002g0236others(12): Show | 15 | HG00741.hp1 HG01109.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.165+3252C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53855316 | ||||||
| chr8:53856034
|
A | C | 3 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231 | 3 | NA18990.hp1 NA19060.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.165+3970A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53856034 | ||||||
| chr8:53856160
|
G | A | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.165+4096G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53856160 | ||||||
| chr8:53856216
|
AT | A | 55 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(52): Show | 55 | HG00323.hp2 HG00741.hp1 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.165+4169delT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53856216 | |||||
| chr8:53856508
|
C | T | 2 | a0001c0001t0002g0227a0001c0001t0002g0228 | 2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.165+4444C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53856508 | ||||||
| chr8:53856523
|
A | C | 1 | a0001c0001t0002g0226 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.165+4459A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53856523 | ||||||
| chr8:53856658
|
T | G | 2 | a0001c0001t0005g0118a0001c0001t0005g0119 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.165+4594T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53856658 | ||||||
| chr8:53857393
|
G | T | 1 | a0001c0001t0001g0087 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.165+5329G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53857393 | ||||||
| chr8:53857413
|
T | C | 1 | a0001c0001t0001g0088 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.165+5349T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53857413 | ||||||
| chr8:53857551
|
G | A | 1 | a0001c0001t0002g0232 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.165+5487G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53857551 | ||||||
| chr8:53857739
|
G | A | 1 | a0001c0001t0001g0120 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.165+5675G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53857739 | ||||||
| chr8:53857747
|
A | G | 89 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(86): Show | 89 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.165+5683A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53857747 | ||||||
| chr8:53857974
|
A | G | 1 | a0001c0001t0002g0111 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.165+5910A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53857974 | ||||||
| chr8:53858265
|
T | C | 1 | a0001c0001t0002g0247 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.165+6201T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53858265 | ||||||
| chr8:53858300
|
C | T | 7 | a0001c0001t0001g0222a0001c0001t0002g0218a0001c0001t0002g0219others(4): Show | 7 | HG00140.hp1 HG01070.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.165+6236C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53858300 | ||||||
| chr8:53858503
|
C | T | 13 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(10): Show | 13 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.165+6439C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53858503 | ||||||
| chr8:53858532
|
C | A | 14 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(11): Show | 14 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+6468C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53858532 | ||||||
| chr8:53858674
|
C | A | 17 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(14): Show | 17 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.165+6610C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53858674 | ||||||
| chr8:53858718
|
T | C | 9 | a0001c0001t0002g0235a0001c0001t0002g0236a0001c0001t0002g0240others(6): Show | 9 | HG00741.hp1 HG01109.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+6654T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53858718 | ||||||
| chr8:53858741
|
G | A | 5 | a0001c0003t0001g0028a0001c0003t0002g0025a0001c0003t0002g0029others(2): Show | 5 | HG02280.hp2 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+6677G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53858741 | ||||||
| chr8:53858845
|
T | G | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.165+6781T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53858845 | ||||||
| chr8:53858892
|
T | TA | 82 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0023others(79): Show | 82 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.165+6848dupA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53858892 | |||||
| chr8:53858892
|
T | TAA | 10 | a0001c0001t0001g0010a0001c0001t0001g0040a0001c0001t0001g0041others(7): Show | 10 | HG00423.hp2 HG00438.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.165+6847_165+6848d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53858892 | |||||
| chr8:53858892
|
TA | T | 13 | a0001c0001t0001g0110a0001c0001t0002g0108a0001c0001t0002g0215others(10): Show | 13 | HG00642.hp1 HG01099.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.165+6848delA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53858892 | |||||
| chr8:53858913
|
C | A | 1 | a0001c0003t0002g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.165+6849C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53858913 | ||||||
| chr8:53859019
|
A | G | 2 | a0001c0003t0002g0025a0001c0003t0002g0029 | 2 | HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.165+6955A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53859019 | ||||||
| chr8:53859209
|
C | G | 1 | a0001c0001t0001g0252 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.165+7145C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53859209 | ||||||
| chr8:53859217
|
A | C | 1 | a0001c0001t0002g0214 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.165+7153A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53859217 | ||||||
| chr8:53859217
|
A | G | 77 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(74): Show | 77 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.165+7153A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53859217 | ||||||
| chr8:53859326
|
T | A | 17 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(14): Show | 17 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.165+7262T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53859326 | ||||||
| chr8:53859422
|
A | AT | 12 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(9): Show | 12 | HG02055.hp2 HG02280.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.165+7362dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53859422 | |||||
| chr8:53859652
|
A | C | 1 | a0001c0001t0002g0016 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.165+7588A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53859652 | ||||||
| chr8:53859673
|
C | G | 1 | a0001c0001t0002g0017 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.165+7609C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53859673 | ||||||
| chr8:53859673
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.165+7609C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53859673 | ||||||
| chr8:53859815
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0125 | 2 | HG02027.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.165+7751G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53859815 | ||||||
| chr8:53859852
|
A | T | 1 | a0001c0001t0002g0212 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.165+7788A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53859852 | ||||||
| chr8:53859907
|
A | T | 1 | a0001c0001t0001g0084 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.165+7843A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53859907 | ||||||
| chr8:53859916
|
C | T | 1 | a0001c0001t0002g0217 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.165+7852C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53859916 | ||||||
| chr8:53859968
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.165+7904A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53859968 | ||||||
| chr8:53859994
|
T | C | 1 | a0001c0001t0002g0242 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.165+7930T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53859994 | ||||||
| chr8:53860374
|
T | C | 60 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0035others(57): Show | 60 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.165+8310T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53860374 | ||||||
| chr8:53860520
|
G | A | 2 | a0001c0001t0002g0108a0001c0001t0003g0109 | 2 | HG02572.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.165+8456G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53860520 | ||||||
| chr8:53860560
|
G | GAAGATGC others(4): Show |
77 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(74): Show | 77 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.165+8501_165+8502i others(13): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53860560 | |||||
| chr8:53860654
|
T | C | 1 | a0001c0001t0001g0120 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.165+8590T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53860654 | ||||||
| chr8:53860692
|
G | A | 8 | a0001c0002t0001g0005a0001c0002t0002g0002a0001c0002t0002g0004others(5): Show | 8 | HG02559.hp1 HG02922.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+8628G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53860692 | ||||||
| chr8:53860708
|
C | G | 256 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(253): Show | 256 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.165+8644C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53860708 | ||||||
| chr8:53860713
|
C | G | 2 | a0001c0001t0007g0033a0001c0001t0007g0045 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.165+8649C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53860713 | ||||||
| chr8:53860844
|
G | A | 2 | a0001c0001t0001g0093a0001c0001t0001g0110 | 2 | NA18959.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.165+8780G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53860844 | ||||||
| chr8:53860982
|
A | T | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.165+8918A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53860982 | ||||||
| chr8:53861114
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.165+9050C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53861114 | ||||||
| chr8:53861311
|
G | A | 1 | a0001c0001t0009g0128 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.165+9247G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53861311 | ||||||
| chr8:53861335
|
C | T | 1 | a0001c0001t0002g0223 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.165+9271C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53861335 | ||||||
| chr8:53861350
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.165+9286G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53861350 | ||||||
| chr8:53861358
|
G | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(9): Show | 12 | HG02055.hp2 HG02280.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.165+9294G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53861358 | ||||||
| chr8:53861381
|
C | T | 1 | a0001c0003t0002g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.165+9317C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53861381 | ||||||
| chr8:53861428
|
A | G | 2 | a0001c0001t0002g0117a0001c0001t0002g0210 | 2 | HG02280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.165+9364A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53861428 | ||||||
| chr8:53861873
|
A | C | 2 | a0001c0001t0002g0227a0001c0001t0002g0228 | 2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.165+9809A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53861873 | ||||||
| chr8:53861949
|
C | T | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.165+9885C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53861949 | ||||||
| chr8:53862036
|
G | A | 1 | a0001c0001t0001g0040 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.165+9972G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53862036 | ||||||
| chr8:53862139
|
A | C | 4 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0007g0033others(1): Show | 4 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+10075A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53862139 | ||||||
| chr8:53862390
|
T | G | 1 | a0001c0001t0002g0129 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.165+10326T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53862390 | ||||||
| chr8:53862679
|
G | C | 8 | a0001c0002t0001g0005a0001c0002t0002g0002a0001c0002t0002g0004others(5): Show | 8 | HG02559.hp1 HG02922.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+10615G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53862679 | ||||||
| chr8:53862794
|
A | G | 9 | a0001c0001t0002g0235a0001c0001t0002g0236a0001c0001t0002g0240others(6): Show | 9 | HG00741.hp1 HG01109.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+10730A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53862794 | ||||||
| chr8:53862868
|
G | T | 8 | a0001c0002t0001g0005a0001c0002t0002g0002a0001c0002t0002g0004others(5): Show | 8 | HG02559.hp1 HG02922.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+10804G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53862868 | ||||||
| chr8:53862953
|
C | T | 2 | a0001c0001t0001g0023a0001c0001t0003g0024 | 2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.165+10889C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53862953 | ||||||
| chr8:53862970
|
A | G | 17 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(14): Show | 17 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.165+10906A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53862970 | ||||||
| chr8:53863032
|
A | G | 1 | a0001c0001t0003g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.165+10968A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53863032 | ||||||
| chr8:53863080
|
C | G | 2 | a0001c0001t0002g0038a0001c0001t0008g0039 | 2 | HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.165+11016C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53863080 | ||||||
| chr8:53863132
|
C | G | 1 | a0001c0001t0001g0015 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.165+11068C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53863132 | ||||||
| chr8:53863229
|
C | T | 1 | a0001c0001t0002g0209 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.165+11165C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53863229 | ||||||
| chr8:53863269
|
G | A | 1 | a0001c0001t0003g0234 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.165+11205G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53863269 | ||||||
| chr8:53863292
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.165+11228A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53863292 | ||||||
| chr8:53863336
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.165+11272C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53863336 | ||||||
| chr8:53863500
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.165+11436G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53863500 | ||||||
| chr8:53863533
|
A | T | 12 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(9): Show | 12 | HG02055.hp2 HG02280.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.165+11469A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53863533 | ||||||
| chr8:53863702
|
T | A | 1 | a0001c0001t0002g0131 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.165+11638T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53863702 | ||||||
| chr8:53863727
|
C | CT | 14 | a0001c0001t0001g0206a0001c0001t0001g0225a0001c0001t0002g0038others(11): Show | 14 | HG00438.hp1 HG01069.hp2 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.165+11682dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53863727 | |||||
| chr8:53863727
|
CT | C | 27 | a0001c0001t0001g0046a0001c0001t0001g0088a0001c0001t0001g0089others(24): Show | 27 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.165+11682delT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53863727 | |||||
| chr8:53863796
|
G | A | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.165+11732G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53863796 | ||||||
| chr8:53863963
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.165+11899G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53863963 | ||||||
| chr8:53864257
|
C | T | 1 | a0001c0003t0001g0028 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.165+12193C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53864257 | ||||||
| chr8:53864277
|
A | C | 1 | a0001c0003t0002g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.165+12213A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53864277 | ||||||
| chr8:53864297
|
G | A | 2 | a0001c0001t0002g0038a0001c0001t0008g0039 | 2 | HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.165+12233G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53864297 | ||||||
| chr8:53864303
|
G | A | 8 | a0001c0002t0001g0005a0001c0002t0002g0002a0001c0002t0002g0004others(5): Show | 8 | HG02559.hp1 HG02922.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+12239G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53864303 | ||||||
| chr8:53864430
|
G | GA | 37 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0047others(34): Show | 37 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.165+12387dupA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53864430 | |||||
| chr8:53864430
|
GA | G | 20 | a0001c0001t0001g0015a0001c0001t0001g0074a0001c0001t0001g0075others(17): Show | 20 | HG01496.hp2 HG02055.hp2 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.165+12387delA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53864430 | |||||
| chr8:53864475
|
T | C | 1 | a0001c0001t0002g0145 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.165+12411T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53864475 | ||||||
| chr8:53865154
|
T | C | 1 | a0001c0005t0002g0113 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.165+13090T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53865154 | ||||||
| chr8:53865184
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0086 | 2 | NA19056.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.165+13120C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53865184 | ||||||
| chr8:53865245
|
G | A | 1 | a0001c0001t0003g0051 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.165+13181G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53865245 | ||||||
| chr8:53865301
|
A | G | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.165+13237A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53865301 | ||||||
| chr8:53865364
|
G | A | 1 | a0001c0001t0002g0146 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.165+13300G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53865364 | ||||||
| chr8:53865422
|
T | C | 12 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(9): Show | 12 | HG02055.hp2 HG02280.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.165+13358T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53865422 | ||||||
| chr8:53865757
|
C | G | 1 | a0001c0001t0002g0144 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.166-13501C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53865757 | ||||||
| chr8:53865862
|
T | C | 65 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0035others(62): Show | 65 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.166-13396T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53865862 | ||||||
| chr8:53865886
|
C | T | 12 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(9): Show | 12 | HG02055.hp2 HG02280.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-13372C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53865886 | ||||||
| chr8:53866042
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.166-13216G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53866042 | ||||||
| chr8:53866053
|
C | T | 12 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(9): Show | 12 | HG02055.hp2 HG02280.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-13205C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53866053 | ||||||
| chr8:53866145
|
G | A | 8 | a0001c0002t0001g0005a0001c0002t0002g0002a0001c0002t0002g0004others(5): Show | 8 | HG02559.hp1 HG02922.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-13113G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53866145 | ||||||
| chr8:53866280
|
C | T | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.166-12978C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53866280 | ||||||
| chr8:53866288
|
G | A | 15 | a0001c0001t0001g0041a0001c0001t0001g0052a0001c0001t0001g0074others(12): Show | 15 | HG00438.hp2 HG01496.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.166-12970G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53866288 | ||||||
| chr8:53866387
|
C | CT | 9 | a0001c0001t0001g0121a0001c0001t0001g0143a0001c0001t0002g0020others(6): Show | 9 | HG01099.hp2 HG02027.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.166-12858dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53866387 | |||||
| chr8:53866387
|
CT | C | 9 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(6): Show | 9 | HG02027.hp2 HG02055.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.166-12858delT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53866387 | |||||
| chr8:53866918
|
C | T | 14 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(11): Show | 14 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.166-12340C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53866918 | ||||||
| chr8:53866957
|
C | T | 89 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(86): Show | 89 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.166-12301C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53866957 | ||||||
| chr8:53866992
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.166-12266G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53866992 | ||||||
| chr8:53867426
|
G | T | 17 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(14): Show | 17 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.166-11832G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53867426 | ||||||
| chr8:53867428
|
C | T | 5 | a0001c0003t0001g0028a0001c0003t0002g0025a0001c0003t0002g0029others(2): Show | 5 | HG02280.hp2 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-11830C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53867428 | ||||||
| chr8:53867518
|
G | A | 1 | a0001c0005t0002g0113 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.166-11740G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53867518 | ||||||
| chr8:53867547
|
G | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0202 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.166-11711G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53867547 | ||||||
| chr8:53867554
|
C | G | 24 | a0001c0001t0001g0018a0001c0001t0001g0088a0001c0001t0001g0089others(21): Show | 24 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.166-11704C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53867554 | ||||||
| chr8:53867614
|
C | T | 77 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(74): Show | 77 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.166-11644C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53867614 | ||||||
| chr8:53867649
|
C | T | 220 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(217): Show | 220 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.166-11609C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53867649 | ||||||
| chr8:53867658
|
T | TCTTC | 87 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0052others(84): Show | 87 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.166-11556_166-1155 others(8): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53867658 | |||||
| chr8:53867658
|
T | TCTTCCTT others(1): Show |
22 | a0001c0001t0001g0018a0001c0001t0001g0093a0001c0001t0001g0110others(19): Show | 22 | HG00140.hp2 HG00438.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.166-11560_166-1155 others(12): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53867658 | |||||
| chr8:53867658
|
T | TCTTCCTT others(5): Show |
2 | a0001c0001t0001g0105a0001c0001t0001g0206 | 2 | HG01261.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.166-11564_166-1155 others(16): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53867658 | |||||
| chr8:53867658
|
TCTTC | T | 34 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0046others(31): Show | 34 | HG00423.hp1 HG01167.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.166-11556_166-1155 others(8): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53867658 | |||||
| chr8:53867706
|
T | C | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.166-11552T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53867706 | ||||||
| chr8:53867711
|
G | C | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.166-11547G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53867711 | ||||||
| chr8:53867945
|
A | G | 1 | a0001c0001t0001g0115 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.166-11313A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53867945 | ||||||
| chr8:53868039
|
T | G | 5 | a0001c0003t0001g0028a0001c0003t0002g0025a0001c0003t0002g0029others(2): Show | 5 | HG02280.hp2 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-11219T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53868039 | ||||||
| chr8:53868484
|
G | C | 1 | a0001c0001t0002g0175 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.166-10774G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53868484 | ||||||
| chr8:53868495
|
G | A | 1 | a0001c0003t0002g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.166-10763G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53868495 | ||||||
| chr8:53868502
|
G | A | 1 | a0001c0001t0001g0018 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.166-10756G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53868502 | ||||||
| chr8:53868653
|
A | AAT | 8 | a0001c0001t0001g0010a0001c0001t0004g0011a0001c0001t0004g0012others(5): Show | 8 | HG02280.hp2 HG02886.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.166-10590_166-1058 others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53868653 | |||||
| chr8:53868653
|
A | AATAT | 3 | a0001c0001t0001g0015a0001c0001t0002g0016a0001c0003t0003g0026 | 3 | HG02055.hp2 HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.166-10592_166-1058 others(8): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53868653 | |||||
| chr8:53868697
|
T | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(9): Show | 12 | HG02055.hp2 HG02280.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-10561T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53868697 | ||||||
| chr8:53868733
|
G | T | 27 | a0001c0001t0001g0018a0001c0001t0001g0088a0001c0001t0001g0089others(24): Show | 27 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.166-10525G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53868733 | ||||||
| chr8:53868909
|
C | T | 1 | a0001c0003t0002g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.166-10349C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53868909 | ||||||
| chr8:53869088
|
A | T | 2 | a0001c0001t0002g0038a0001c0001t0008g0039 | 2 | HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.166-10170A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53869088 | ||||||
| chr8:53869414
|
G | A | 61 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0035others(58): Show | 61 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.166-9844G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53869414 | ||||||
| chr8:53869530
|
G | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.166-9728G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53869530 | ||||||
| chr8:53869568
|
C | T | 1 | a0001c0001t0002g0145 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.166-9690C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53869568 | ||||||
| chr8:53869591
|
G | A | 4 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0007g0033others(1): Show | 4 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-9667G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53869591 | ||||||
| chr8:53869605
|
T | G | 90 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(87): Show | 90 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.166-9653T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53869605 | ||||||
| chr8:53869611
|
G | T | 1 | a0001c0001t0001g0101 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.166-9647G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53869611 | ||||||
| chr8:53869632
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.166-9626C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53869632 | ||||||
| chr8:53869746
|
C | T | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.166-9512C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53869746 | ||||||
| chr8:53869869
|
G | A | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.166-9389G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53869869 | ||||||
| chr8:53869871
|
G | T | 2 | a0001c0001t0002g0174a0001c0001t0002g0209 | 2 | NA18961.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.166-9387G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53869871 | ||||||
| chr8:53869956
|
C | A | 6 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0056others(3): Show | 6 | NA18963.hp2 NA19055.hp2 NA19056.hp2 others(3): Show |
intron_variant | MODIFIER | c.166-9302C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53869956 | ||||||
| chr8:53870022
|
A | T | 1 | a0001c0001t0001g0084 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.166-9236A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53870022 | ||||||
| chr8:53870108
|
A | G | 17 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(14): Show | 17 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.166-9150A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53870108 | ||||||
| chr8:53870244
|
T | C | 1 | a0001c0001t0002g0070 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.166-9014T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53870244 | ||||||
| chr8:53870262
|
T | TAC | 4 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0007g0033others(1): Show | 4 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-8976_166-8975d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53870262 | |||||
| chr8:53870452
|
C | T | 4 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0007g0033others(1): Show | 4 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-8806C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53870452 | ||||||
| chr8:53870573
|
A | T | 3 | a0001c0001t0002g0038a0001c0001t0008g0039a0001c0003t0002g0253 | 3 | HG02109.hp2 HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.166-8685A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53870573 | ||||||
| chr8:53870641
|
T | C | 2 | a0001c0001t0002g0038a0001c0001t0008g0039 | 2 | HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.166-8617T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53870641 | ||||||
| chr8:53870679
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.166-8579C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53870679 | ||||||
| chr8:53870895
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.166-8363G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53870895 | ||||||
| chr8:53871035
|
C | T | 8 | a0001c0002t0001g0005a0001c0002t0002g0002a0001c0002t0002g0004others(5): Show | 8 | HG02559.hp1 HG02922.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-8223C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53871035 | ||||||
| chr8:53871112
|
C | CA | 67 | a0001c0001t0001g0031a0001c0001t0001g0035a0001c0001t0001g0040others(64): Show | 67 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.166-8117dupA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53871112 | |||||
| chr8:53871112
|
C | CAA | 11 | a0001c0001t0001g0023a0001c0001t0001g0047a0001c0001t0001g0125others(8): Show | 11 | HG00597.hp1 HG01169.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.166-8118_166-8117d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53871112 | |||||
| chr8:53871112
|
CA | C | 24 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(21): Show | 24 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.166-8117delA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53871112 | |||||
| chr8:53871112
|
CAA | C | 5 | a0001c0002t0001g0005a0001c0002t0002g0006a0001c0002t0002g0007others(2): Show | 5 | HG02922.hp1 HG03041.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-8118_166-8117d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53871112 | |||||
| chr8:53871112
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0213 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.166-8126_166-8117d others(12): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53871112 | |||||
| chr8:53871112
|
CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0002g0038a0001c0001t0008g0039a0001c0003t0002g0253 | 3 | HG02109.hp2 HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.166-8127_166-8117d others(13): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53871112 | |||||
| chr8:53871247
|
C | A | 3 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091 | 3 | HG00423.hp2 HG04184.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.166-8011C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53871247 | ||||||
| chr8:53871512
|
G | C | 1 | a0001c0001t0001g0256 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.166-7746G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53871512 | ||||||
| chr8:53871624
|
A | T | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | NA18957.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.166-7634A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53871624 | ||||||
| chr8:53871624
|
AAAT | A | 90 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(87): Show | 90 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.166-7618_166-7616d others(5): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53871624 | |||||
| chr8:53871627
|
T | A | 2 | a0001c0001t0001g0137a0001c0001t0001g0184 | 2 | NA18948.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.166-7631T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53871627 | ||||||
| chr8:53871630
|
T | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(4): Show | 7 | HG02055.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-7628T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53871630 | ||||||
| chr8:53871631
|
A | G | 1 | a0001c0001t0002g0176 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.166-7627A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53871631 | ||||||
| chr8:53871707
|
A | G | 2 | a0001c0001t0001g0023a0001c0001t0003g0024 | 2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.166-7551A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53871707 | ||||||
| chr8:53871824
|
C | T | 1 | a0001c0003t0002g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.166-7434C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53871824 | ||||||
| chr8:53871877
|
T | G | 253 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(250): Show | 253 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.166-7381T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53871877 | ||||||
| chr8:53871936
|
C | T | 1 | a0001c0003t0002g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.166-7322C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53871936 | ||||||
| chr8:53872222
|
T | A | 1 | a0001c0003t0001g0028 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.166-7036T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53872222 | ||||||
| chr8:53872394
|
C | A | 1 | a0001c0003t0001g0028 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.166-6864C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53872394 | ||||||
| chr8:53872650
|
A | G | 1 | a0001c0001t0002g0038 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.166-6608A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53872650 | ||||||
| chr8:53872780
|
C | G | 1 | a0001c0001t0001g0123 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.166-6478C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53872780 | ||||||
| chr8:53872839
|
T | G | 1 | a0001c0001t0002g0139 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.166-6419T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53872839 | ||||||
| chr8:53872869
|
C | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(4): Show | 7 | HG02055.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-6389C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53872869 | ||||||
| chr8:53872901
|
A | C | 1 | a0001c0001t0002g0183 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.166-6357A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53872901 | ||||||
| chr8:53873130
|
C | T | 61 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0035others(58): Show | 61 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.166-6128C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53873130 | ||||||
| chr8:53873369
|
A | G | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.166-5889A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53873369 | ||||||
| chr8:53873625
|
C | A | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.166-5633C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53873625 | ||||||
| chr8:53873781
|
G | A | 62 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0035others(59): Show | 62 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.166-5477G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53873781 | ||||||
| chr8:53873915
|
C | T | 62 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0035others(59): Show | 62 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.166-5343C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53873915 | ||||||
| chr8:53873924
|
T | C | 2 | a0001c0001t0001g0060a0001c0001t0002g0073 | 2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.166-5334T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53873924 | ||||||
| chr8:53874061
|
G | A | 2 | a0001c0001t0002g0174a0001c0001t0002g0209 | 2 | NA18961.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.166-5197G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874061 | ||||||
| chr8:53874129
|
G | A | 61 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0035others(58): Show | 61 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.166-5129G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874129 | ||||||
| chr8:53874149
|
C | T | 12 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(9): Show | 12 | HG02055.hp2 HG02280.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-5109C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874149 | ||||||
| chr8:53874154
|
A | T | 1 | a0001c0003t0004g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.166-5104A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874154 | ||||||
| chr8:53874173
|
C | T | 62 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0035others(59): Show | 62 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.166-5085C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874173 | ||||||
| chr8:53874367
|
G | GGT | 25 | a0001c0001t0001g0010a0001c0001t0001g0143a0001c0001t0001g0193others(22): Show | 25 | HG00323.hp1 HG00741.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.166-4857_166-4856d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53874367 | |||||
| chr8:53874367
|
G | GGTGT | 8 | a0001c0001t0002g0117a0001c0001t0002g0132a0001c0001t0002g0144others(5): Show | 8 | HG01891.hp2 HG01978.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-4859_166-4856d others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53874367 | |||||
| chr8:53874367
|
G | GT | 4 | a0001c0001t0001g0107a0001c0001t0002g0182a0001c0001t0002g0216others(1): Show | 4 | HG01099.hp1 HG01168.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-4891_166-4890i others(3): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874367 | ||||||
| chr8:53874367
|
GGT | G | 24 | a0001c0001t0001g0115a0001c0001t0001g0148a0001c0001t0001g0156others(21): Show | 24 | HG00408.hp1 HG00408.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.166-4857_166-4856d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53874367 | |||||
| chr8:53874367
|
GGTGT | G | 15 | a0001c0001t0001g0014a0001c0001t0001g0123a0001c0001t0001g0152others(12): Show | 15 | HG00438.hp1 HG01069.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.166-4859_166-4856d others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53874367 | |||||
| chr8:53874367
|
GGTGTGTG others(3): Show |
G | 1 | a0001c0001t0002g0175 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.166-4865_166-4856d others(12): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53874367 | |||||
| chr8:53874367
|
GGTGTGTG others(5): Show |
G | 1 | a0001c0003t0002g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.166-4867_166-4856d others(14): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53874367 | |||||
| chr8:53874369
|
T | G | 1 | a0001c0001t0001g0121 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.166-4889T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874369 | ||||||
| chr8:53874391
|
TGTGTGTG others(5): Show |
T | 3 | a0001c0001t0001g0048a0001c0001t0003g0030a0001c0001t0004g0037 | 3 | HG01167.hp1 HG02630.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.166-4865_166-4854d others(14): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53874391 | |||||
| chr8:53874393
|
TGTGTGTG others(3): Show |
T | 56 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0035others(53): Show | 56 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.166-4863_166-4854d others(12): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53874393 | |||||
| chr8:53874399
|
T | C | 1 | a0001c0003t0002g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.166-4859T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874399 | ||||||
| chr8:53874401
|
T | C | 6 | a0001c0001t0001g0156a0001c0001t0002g0146a0001c0001t0002g0157others(3): Show | 6 | HG01358.hp2 HG02109.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.166-4857T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874401 | ||||||
| chr8:53874407
|
C | T | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG02165.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.166-4851C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874407 | ||||||
| chr8:53874411
|
T | C | 62 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0035others(59): Show | 62 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.166-4847T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874411 | ||||||
| chr8:53874416
|
T | A | 62 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0035others(59): Show | 62 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.166-4842T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874416 | ||||||
| chr8:53874519
|
G | C | 5 | a0001c0003t0001g0028a0001c0003t0002g0025a0001c0003t0002g0029others(2): Show | 5 | HG02280.hp2 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-4739G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874519 | ||||||
| chr8:53874585
|
A | G | 62 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0035others(59): Show | 62 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.166-4673A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874585 | ||||||
| chr8:53874763
|
T | C | 1 | a0001c0001t0002g0117 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.166-4495T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874763 | ||||||
| chr8:53874820
|
T | G | 1 | a0001c0003t0002g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.166-4438T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874820 | ||||||
| chr8:53874838
|
A | C | 1 | a0001c0001t0001g0101 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.166-4420A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874838 | ||||||
| chr8:53874901
|
A | C | 1 | a0001c0003t0002g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.166-4357A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874901 | ||||||
| chr8:53875009
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.166-4249C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53875009 | ||||||
| chr8:53875014
|
A | G | 5 | a0001c0003t0001g0028a0001c0003t0002g0025a0001c0003t0002g0029others(2): Show | 5 | HG02280.hp2 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-4244A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53875014 | ||||||
| chr8:53875025
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.166-4233C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53875025 | ||||||
| chr8:53875044
|
A | C | 2 | a0001c0001t0002g0038a0001c0001t0008g0039 | 2 | HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.166-4214A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53875044 | ||||||
| chr8:53875071
|
G | C | 5 | a0001c0003t0001g0028a0001c0003t0002g0025a0001c0003t0002g0029others(2): Show | 5 | HG02280.hp2 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-4187G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53875071 | ||||||
| chr8:53875125
|
A | G | 1 | a0001c0003t0002g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.166-4133A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53875125 | ||||||
| chr8:53875191
|
T | G | 62 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0035others(59): Show | 62 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.166-4067T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53875191 | ||||||
| chr8:53875233
|
A | G | 12 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0007g0033others(9): Show | 12 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.166-4025A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53875233 | ||||||
| chr8:53875429
|
C | CA | 44 | a0001c0001t0001g0089a0001c0001t0001g0095a0001c0001t0001g0121others(41): Show | 44 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.166-3808dupA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53875429 | |||||
| chr8:53875429
|
C | CAAAA | 5 | a0001c0001t0001g0015a0001c0001t0002g0016a0001c0001t0002g0021others(2): Show | 5 | HG02055.hp2 HG02895.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.166-3811_166-3808d others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53875429 | |||||
| chr8:53875429
|
CA | C | 5 | a0001c0001t0001g0116a0001c0001t0001g0156a0001c0001t0002g0192others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.166-3808delA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53875429 | |||||
| chr8:53875448
|
AAACC | A | 45 | a0001c0001t0001g0031a0001c0001t0001g0035a0001c0001t0001g0036others(42): Show | 45 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.166-3807_166-3804d others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53875448 | |||||
| chr8:53875449
|
AACC | A | 14 | a0001c0001t0001g0023a0001c0001t0001g0049a0001c0001t0001g0061others(11): Show | 14 | HG00609.hp2 HG02074.hp2 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.166-3807_166-3805d others(5): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53875449 | |||||
| chr8:53875451
|
C | A | 1 | a0001c0001t0006g0043 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.166-3807C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53875451 | ||||||
| chr8:53875452
|
C | A | 1 | a0001c0001t0001g0204 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.166-3806C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53875452 | ||||||
| chr8:53875460
|
C | A | 5 | a0001c0001t0002g0165a0001c0001t0002g0232a0001c0001t0004g0011others(2): Show | 5 | HG02004.hp2 HG02723.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-3798C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53875460 | ||||||
| chr8:53875691
|
T | C | 90 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(87): Show | 90 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.166-3567T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53875691 | ||||||
| chr8:53875895
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.166-3363C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53875895 | ||||||
| chr8:53876010
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.166-3248G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53876010 | ||||||
| chr8:53876537
|
C | T | 5 | a0001c0001t0002g0117a0001c0001t0002g0196a0001c0001t0002g0210others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-2721C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53876537 | ||||||
| chr8:53876672
|
T | C | 9 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(6): Show | 9 | HG02055.hp2 HG02572.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.166-2586T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53876672 | ||||||
| chr8:53876755
|
G | A | 1 | a0001c0001t0003g0170 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.166-2503G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53876755 | ||||||
| chr8:53877237
|
G | T | 58 | a0001c0001t0001g0031a0001c0001t0001g0035a0001c0001t0001g0036others(55): Show | 58 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.166-2021G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53877237 | ||||||
| chr8:53877268
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.166-1990C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53877268 | ||||||
| chr8:53877276
|
G | A | 72 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(69): Show | 72 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.166-1982G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53877276 | ||||||
| chr8:53877350
|
G | A | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.166-1908G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53877350 | ||||||
| chr8:53877368
|
G | A | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.166-1890G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53877368 | ||||||
| chr8:53877379
|
C | G | 7 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(4): Show | 7 | HG02055.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-1879C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53877379 | ||||||
| chr8:53877380
|
C | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(4): Show | 7 | HG02055.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-1878C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53877380 | ||||||
| chr8:53877407
|
C | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(4): Show | 7 | HG02055.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-1851C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53877407 | ||||||
| chr8:53877507
|
C | T | 61 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0035others(58): Show | 61 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.166-1751C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53877507 | ||||||
| chr8:53877516
|
G | T | 1 | a0001c0001t0001g0060 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.166-1742G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53877516 | ||||||
| chr8:53877922
|
C | G | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.166-1336C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53877922 | ||||||
| chr8:53878065
|
C | G | 1 | a0001c0001t0004g0037 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.166-1193C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53878065 | ||||||
| chr8:53878137
|
C | G | 1 | a0001c0001t0002g0134 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.166-1121C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53878137 | ||||||
| chr8:53878429
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.166-829C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53878429 | ||||||
| chr8:53878461
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.166-797T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53878461 | ||||||
| chr8:53878490
|
G | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(4): Show | 7 | HG02055.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-768G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53878490 | ||||||
| chr8:53878737
|
G | C | 7 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(4): Show | 7 | HG02055.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-521G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53878737 | ||||||
| chr8:53878773
|
C | G | 4 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0007g0033others(1): Show | 4 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-485C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53878773 | ||||||
| chr8:53878927
|
C | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(4): Show | 7 | HG02055.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-331C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53878927 | ||||||
| chr8:53879675
|
A | G | 19 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0040others(16): Show | 19 | HG00609.hp2 HG01993.hp1 NA18612.hp2 others(16): Show |
intron_variant | MODIFIER | c.510+73A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53879675 | ||||||
| chr8:53879783
|
G | A | 1 | a0001c0001t0002g0165 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.510+181G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53879783 | ||||||
| chr8:53879903
|
T | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(4): Show | 7 | HG02055.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.510+301T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53879903 | ||||||
| chr8:53879942
|
C | A | 1 | a0001c0001t0003g0170 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.510+340C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53879942 | ||||||
| chr8:53879959
|
G | A | 1 | a0001c0001t0002g0094 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.510+357G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53879959 | ||||||
| chr8:53880299
|
C | T | 1 | a0001c0001t0001g0067 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.510+697C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53880299 | ||||||
| chr8:53880670
|
G | A | 4 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0007g0033others(1): Show | 4 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+1068G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53880670 | ||||||
| chr8:53880675
|
G | C | 66 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0035others(63): Show | 66 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.510+1073G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53880675 | ||||||
| chr8:53881024
|
G | C | 1 | a0001c0001t0002g0126 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.510+1422G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53881024 | ||||||
| chr8:53881176
|
G | C | 17 | a0001c0001t0001g0088a0001c0001t0001g0092a0001c0001t0001g0093others(14): Show | 17 | HG00597.hp2 HG00642.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.510+1574G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53881176 | ||||||
| chr8:53881223
|
C | CCGGTGCG others(19): Show |
1 | a0001c0002t0001g0005 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.510+1641_510+1642i others(28): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53881223 | |||||
| chr8:53881223
|
C | CCGGTGCG others(19): Show |
7 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(4): Show | 7 | HG02559.hp1 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+1623_510+1648d others(28): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53881223 | |||||
| chr8:53881273
|
G | C | 1 | a0001c0001t0002g0203 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.510+1671G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53881273 | ||||||
| chr8:53881368
|
T | C | 86 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(83): Show | 86 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.510+1766T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53881368 | ||||||
| chr8:53881437
|
C | T | 6 | a0001c0003t0001g0028a0001c0003t0002g0025a0001c0003t0002g0029others(3): Show | 6 | HG02109.hp2 HG02280.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+1835C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53881437 | ||||||
| chr8:53881443
|
G | A | 1 | a0001c0001t0002g0182 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.510+1841G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53881443 | ||||||
| chr8:53881552
|
G | A | 1 | a0001c0001t0002g0176 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.510+1950G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53881552 | ||||||
| chr8:53881927
|
G | A | 2 | a0001c0001t0002g0227a0001c0001t0002g0228 | 2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.510+2325G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53881927 | ||||||
| chr8:53882151
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.510+2549G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53882151 | ||||||
| chr8:53882450
|
T | A | 10 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0002t0001g0005others(7): Show | 10 | HG02559.hp1 HG02572.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.510+2848T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53882450 | ||||||
| chr8:53882582
|
T | C | 5 | a0001c0003t0001g0028a0001c0003t0002g0025a0001c0003t0002g0029others(2): Show | 5 | HG02280.hp2 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+2980T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53882582 | ||||||
| chr8:53882643
|
C | CA | 67 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0035others(64): Show | 67 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.510+3059dupA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53882643 | |||||
| chr8:53882643
|
C | CAA | 8 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0056others(5): Show | 8 | HG03209.hp1 NA18963.hp2 NA18994.hp1 others(5): Show |
intron_variant | MODIFIER | c.510+3058_510+3059d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53882643 | |||||
| chr8:53882643
|
C | CAAA | 14 | a0001c0001t0001g0010a0001c0001t0002g0020a0001c0001t0002g0021others(11): Show | 14 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.510+3057_510+3059d others(5): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53882643 | |||||
| chr8:53882643
|
C | CAAAA | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0004g0011others(2): Show | 5 | HG02055.hp2 HG03453.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+3056_510+3059d others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53882643 | |||||
| chr8:53882643
|
CA | C | 8 | a0001c0001t0001g0138a0001c0001t0001g0202a0001c0001t0001g0229others(5): Show | 8 | HG00621.hp2 HG01167.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.510+3059delA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53882643 | |||||
| chr8:53882681
|
T | C | 63 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0035others(60): Show | 63 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.510+3079T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53882681 | ||||||
| chr8:53882789
|
G | C | 1 | a0001c0001t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.510+3187G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53882789 | ||||||
| chr8:53883108
|
G | T | 85 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(82): Show | 85 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.510+3506G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53883108 | ||||||
| chr8:53883157
|
C | A | 7 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0006others(4): Show | 7 | HG02559.hp1 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+3555C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53883157 | ||||||
| chr8:53883158
|
T | A | 1 | a0001c0002t0001g0005 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.510+3556T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53883158 | ||||||
| chr8:53883158
|
T | C | 1 | a0001c0001t0002g0219 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.510+3556T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53883158 | ||||||
| chr8:53883160
|
T | TC | 61 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0035others(58): Show | 61 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.510+3558_510+3559i others(3): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53883160 | ||||||
| chr8:53883275
|
G | A | 3 | a0001c0001t0002g0179a0001c0001t0002g0183a0001c0001t0008g0114 | 3 | HG02647.hp2 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.510+3673G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53883275 | ||||||
| chr8:53883444
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.510+3842G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53883444 | ||||||
| chr8:53883900
|
G | A | 8 | a0001c0002t0001g0005a0001c0002t0002g0002a0001c0002t0002g0004others(5): Show | 8 | HG02559.hp1 HG02922.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.510+4298G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53883900 | ||||||
| chr8:53883946
|
C | CA | 68 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(65): Show | 68 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.510+4357dupA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53883946 | |||||
| chr8:53884191
|
C | CT | 32 | a0001c0001t0001g0018a0001c0001t0001g0096a0001c0001t0001g0100others(29): Show | 32 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.510+4611dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53884191 | |||||
| chr8:53884191
|
C | CTT | 18 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(15): Show | 18 | HG02055.hp2 HG02132.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.510+4610_510+4611d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53884191 | |||||
| chr8:53884191
|
C | CTTT | 46 | a0001c0001t0001g0031a0001c0001t0001g0035a0001c0001t0001g0036others(43): Show | 46 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.510+4609_510+4611d others(5): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53884191 | |||||
| chr8:53884191
|
C | CTTTT | 14 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0054others(11): Show | 14 | HG00438.hp2 HG02027.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.510+4608_510+4611d others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53884191 | |||||
| chr8:53884191
|
C | CTTTTT | 8 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0002t0001g0005others(5): Show | 8 | HG02559.hp1 HG02572.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.510+4607_510+4611d others(7): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53884191 | |||||
| chr8:53884191
|
CT | C | 6 | a0001c0001t0001g0137a0001c0001t0001g0184a0001c0001t0001g0202others(3): Show | 6 | HG00741.hp2 HG01167.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.510+4611delT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53884191 | |||||
| chr8:53884230
|
C | G | 1 | a0001c0001t0002g0164 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.510+4628C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53884230 | ||||||
| chr8:53884392
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.510+4790C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53884392 | ||||||
| chr8:53884642
|
A | G | 8 | a0001c0002t0001g0005a0001c0002t0002g0002a0001c0002t0002g0004others(5): Show | 8 | HG02559.hp1 HG02922.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.510+5040A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53884642 | ||||||
| chr8:53884907
|
G | A | 1 | a0001c0005t0002g0113 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.510+5305G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53884907 | ||||||
| chr8:53885184
|
C | G | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.510+5582C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53885184 | ||||||
| chr8:53885244
|
C | G | 1 | a0001c0001t0001g0052 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.510+5642C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53885244 | ||||||
| chr8:53885343
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.510+5741G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53885343 | ||||||
| chr8:53885367
|
A | G | 63 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0035others(60): Show | 63 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.510+5765A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53885367 | ||||||
| chr8:53885502
|
T | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0098 | 2 | NA18975.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.510+5900T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53885502 | ||||||
| chr8:53885613
|
C | CA | 11 | a0001c0001t0001g0121a0001c0001t0002g0038a0001c0001t0008g0039others(8): Show | 11 | HG02027.hp1 HG02559.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.510+6022dupA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53885613 | |||||
| chr8:53885736
|
A | G | 1 | a0001c0001t0002g0154 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.510+6134A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53885736 | ||||||
| chr8:53885790
|
C | CT | 18 | a0001c0001t0001g0091a0001c0001t0001g0120a0001c0001t0001g0143others(15): Show | 18 | HG00609.hp1 HG00642.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.510+6210dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53885790 | |||||
| chr8:53885790
|
C | CTT | 6 | a0001c0001t0002g0117a0001c0001t0002g0144a0001c0001t0002g0196others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+6209_510+6210d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53885790 | |||||
| chr8:53885790
|
CT | C | 72 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0031others(69): Show | 72 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.510+6210delT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53885790 | |||||
| chr8:53885790
|
CTT | C | 13 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0035others(10): Show | 13 | HG01070.hp2 HG01167.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.510+6209_510+6210d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53885790 | |||||
| chr8:53885790
|
CTTT | C | 8 | a0001c0002t0001g0005a0001c0002t0002g0002a0001c0002t0002g0004others(5): Show | 8 | HG02109.hp2 HG02559.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.510+6208_510+6210d others(5): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53885790 | |||||
| chr8:53885790
|
CTTTTT | C | 8 | a0001c0001t0002g0243a0001c0001t0002g0244a0001c0001t0002g0245others(5): Show | 8 | HG02280.hp2 HG02486.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.510+6206_510+6210d others(7): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53885790 | |||||
| chr8:53885790
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0002g0168a0001c0001t0002g0173 | 2 | HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.510+6199_510+6210d others(14): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53885790 | |||||
| chr8:53885887
|
TAGAC | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(4): Show | 7 | HG02055.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.510+6289_510+6292d others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53885887 | |||||
| chr8:53885898
|
A | T | 59 | a0001c0001t0001g0095a0001c0001t0001g0105a0001c0001t0001g0112others(56): Show | 59 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.510+6296A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53885898 | ||||||
| chr8:53886147
|
G | A | 1 | a0001c0001t0001g0180 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.510+6545G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53886147 | ||||||
| chr8:53886662
|
G | A | 11 | a0001c0001t0002g0169a0001c0001t0002g0232a0001c0001t0002g0235others(8): Show | 11 | HG00741.hp1 HG01109.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.510+7060G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53886662 | ||||||
| chr8:53887100
|
C | T | 21 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0242others(18): Show | 21 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.510+7498C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53887100 | ||||||
| chr8:53887110
|
T | C | 1 | a0001c0001t0002g0214 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.510+7508T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53887110 | ||||||
| chr8:53887164
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.510+7562G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53887164 | ||||||
| chr8:53887177
|
C | G | 1 | a0001c0001t0002g0209 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.510+7575C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53887177 | ||||||
| chr8:53887221
|
T | A | 2 | a0001c0001t0002g0244a0001c0003t0003g0026 | 2 | HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.510+7619T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53887221 | ||||||
| chr8:53887489
|
G | A | 62 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0035others(59): Show | 62 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.510+7887G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53887489 | ||||||
| chr8:53887813
|
T | C | 1 | a0001c0001t0009g0128 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.510+8211T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53887813 | ||||||
| chr8:53887867
|
A | G | 16 | a0001c0001t0001g0041a0001c0001t0001g0052a0001c0001t0001g0064others(13): Show | 16 | HG00438.hp2 HG01496.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.510+8265A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53887867 | ||||||
| chr8:53887978
|
TA | T | 9 | a0001c0001t0002g0242a0001c0002t0001g0005a0001c0002t0002g0002others(6): Show | 9 | HG02257.hp2 HG02559.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.510+8388delA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53887978 | |||||
| chr8:53888219
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.510+8617G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53888219 | ||||||
| chr8:53888767
|
T | C | 122 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(119): Show | 122 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.510+9165T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53888767 | ||||||
| chr8:53888886
|
C | T | 8 | a0001c0001t0002g0134a0001c0001t0002g0243a0001c0001t0002g0244others(5): Show | 8 | HG02280.hp2 HG02486.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.510+9284C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53888886 | ||||||
| chr8:53888986
|
G | A | 2 | a0001c0001t0006g0043a0001c0001t0006g0044 | 2 | HG01069.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.510+9384G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53888986 | ||||||
| chr8:53889223
|
T | A | 1 | a0001c0001t0001g0099 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.510+9621T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889223 | ||||||
| chr8:53889242
|
G | A | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.510+9640G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889242 | ||||||
| chr8:53889408
|
CTCTCTTT others(9): Show |
C | 1 | a0001c0001t0002g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.510+9808_510+9823d others(18): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889408 | |||||
| chr8:53889408
|
CTCTCTTT others(12): Show |
C | 1 | a0001c0001t0003g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.510+9808_510+9826d others(21): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889408 | |||||
| chr8:53889412
|
C | CT | 27 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0042others(24): Show | 27 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.510+9849dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | |||||
| chr8:53889412
|
C | CTT | 16 | a0001c0001t0001g0036a0001c0001t0001g0050a0001c0001t0001g0055others(13): Show | 16 | HG01192.hp1 HG02572.hp1 HG02602.hp1 others(13): Show |
intron_variant | MODIFIER | c.510+9848_510+9849d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | |||||
| chr8:53889412
|
C | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0211 | 2 | HG00621.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.510+9810C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889412 | ||||||
| chr8:53889412
|
CT | C | 36 | a0001c0001t0001g0018a0001c0001t0001g0093a0001c0001t0001g0095others(33): Show | 36 | HG00140.hp1 HG00621.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.510+9849delT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | |||||
| chr8:53889412
|
CTT | C | 16 | a0001c0001t0001g0123a0001c0001t0001g0148a0001c0001t0001g0166others(13): Show | 16 | HG00140.hp2 HG01261.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.510+9848_510+9849d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | |||||
| chr8:53889412
|
CTTTTTTT | C | 21 | a0001c0001t0001g0121a0001c0001t0001g0254a0001c0001t0001g0255others(18): Show | 21 | HG01192.hp2 HG01243.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.510+9843_510+9849d others(9): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | |||||
| chr8:53889412
|
CTTTTTTT others(1): Show |
C | 14 | a0001c0001t0001g0023a0001c0001t0002g0173a0001c0001t0002g0176others(11): Show | 14 | HG02109.hp1 HG02559.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.510+9842_510+9849d others(10): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | |||||
| chr8:53889412
|
CTTTTTTT others(2): Show |
C | 7 | a0001c0001t0002g0104a0001c0001t0002g0243a0001c0001t0002g0246others(4): Show | 7 | HG01978.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+9841_510+9849d others(11): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | |||||
| chr8:53889412
|
CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0001g0010a0001c0001t0001g0088a0001c0001t0001g0225others(1): Show | 4 | HG02074.hp2 HG02970.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+9840_510+9849d others(12): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | |||||
| chr8:53889412
|
CTTTTTTT others(4): Show |
C | 14 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0098others(11): Show | 14 | HG00642.hp2 HG01099.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.510+9839_510+9849d others(13): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | |||||
| chr8:53889412
|
CTTTTTTT others(5): Show |
C | 7 | a0001c0001t0001g0101a0001c0001t0001g0110a0001c0001t0001g0189others(4): Show | 7 | HG00609.hp1 HG02895.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+9838_510+9849d others(14): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | |||||
| chr8:53889412
|
CTTTTTTT others(6): Show |
C | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0038others(2): Show | 5 | HG02055.hp2 HG02809.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.510+9837_510+9849d others(15): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | |||||
| chr8:53889412
|
CTTTTTTT others(7): Show |
C | 4 | a0001c0001t0002g0242a0001c0001t0004g0037a0001c0001t0006g0043others(1): Show | 4 | HG01069.hp2 HG01167.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+9836_510+9849d others(16): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | |||||
| chr8:53889412
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0007g0045 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.510+9835_510+9849d others(17): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | |||||
| chr8:53889412
|
CTTTTTTT others(9): Show |
C | 15 | a0001c0001t0001g0052a0001c0001t0001g0064a0001c0001t0001g0074others(12): Show | 15 | HG01070.hp2 HG01496.hp2 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.510+9834_510+9849d others(18): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | |||||
| chr8:53889412
|
CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0001g0078 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.510+9833_510+9849d others(19): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | |||||
| chr8:53889412
|
CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0002g0124 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.510+9832_510+9849d others(20): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | |||||
| chr8:53889412
|
CTTTTTTT others(16): Show |
C | 2 | a0001c0001t0003g0001a0001c0002t0003g0003 | 2 | NA19030.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.510+9827_510+9849d others(25): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | |||||
| chr8:53889414
|
T | C | 4 | a0001c0001t0002g0146a0001c0001t0002g0157a0001c0001t0002g0158others(1): Show | 4 | HG01358.hp2 HG03239.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+9812T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889414 | ||||||
| chr8:53889415
|
T | C | 2 | a0001c0001t0001g0201a0001c0001t0002g0212 | 2 | HG03688.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.510+9813T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889415 | ||||||
| chr8:53889416
|
T | C | 1 | a0001c0001t0001g0166 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.510+9814T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889416 | ||||||
| chr8:53889420
|
T | C | 1 | a0001c0001t0002g0132 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.510+9818T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889420 | ||||||
| chr8:53889421
|
T | C | 20 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0002g0032others(17): Show | 20 | HG01192.hp2 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.510+9819T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889421 | ||||||
| chr8:53889422
|
T | C | 12 | a0001c0001t0001g0023a0001c0001t0002g0132a0001c0001t0002g0173others(9): Show | 12 | HG02109.hp1 HG02559.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.510+9820T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889422 | ||||||
| chr8:53889423
|
T | C | 22 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0002g0032others(19): Show | 22 | HG01192.hp2 HG01243.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.510+9821T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889423 | ||||||
| chr8:53889424
|
T | C | 13 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0002g0132others(10): Show | 13 | HG02109.hp1 HG02559.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.510+9822T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889424 | ||||||
| chr8:53889425
|
T | C | 23 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0002g0032others(20): Show | 23 | HG01192.hp2 HG01243.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.510+9823T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889425 | ||||||
| chr8:53889426
|
T | C | 15 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0002g0016others(12): Show | 15 | HG02109.hp1 HG02559.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.510+9824T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889426 | ||||||
| chr8:53889427
|
T | C | 8 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0038others(5): Show | 8 | HG02055.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.510+9825T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889427 | ||||||
| chr8:53889428
|
T | C | 8 | a0001c0001t0001g0010a0001c0001t0002g0016a0001c0001t0002g0242others(5): Show | 8 | HG01069.hp2 HG01167.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.510+9826T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889428 | ||||||
| chr8:53889429
|
T | C | 6 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0038others(3): Show | 6 | HG01071.hp2 HG02055.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.510+9827T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889429 | ||||||
| chr8:53889430
|
T | C | 19 | a0001c0001t0001g0052a0001c0001t0001g0064a0001c0001t0001g0074others(16): Show | 19 | HG01069.hp2 HG01070.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.510+9828T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889430 | ||||||
| chr8:53889431
|
T | C | 2 | a0001c0001t0001g0078a0001c0001t0007g0045 | 2 | HG01071.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.510+9829T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889431 | ||||||
| chr8:53889432
|
T | C | 15 | a0001c0001t0001g0052a0001c0001t0001g0064a0001c0001t0001g0074others(12): Show | 15 | HG01070.hp2 HG01496.hp2 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.510+9830T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889432 | ||||||
| chr8:53889433
|
T | C | 1 | a0001c0001t0001g0078 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.510+9831T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889433 | ||||||
| chr8:53889434
|
T | C | 14 | a0001c0001t0001g0052a0001c0001t0001g0064a0001c0001t0001g0074others(11): Show | 14 | HG01496.hp2 HG02132.hp2 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.510+9832T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889434 | ||||||
| chr8:53889435
|
T | C | 1 | a0001c0001t0001g0078 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.510+9833T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889435 | ||||||
| chr8:53889467
|
T | C | 1 | a0001c0001t0001g0166 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.510+9865T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889467 | ||||||
| chr8:53889504
|
C | T | 1 | a0001c0001t0002g0176 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.510+9902C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889504 | ||||||
| chr8:53889574
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.510+9972G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889574 | ||||||
| chr8:53889645
|
C | T | 1 | a0001c0003t0002g0029 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.510+10043C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889645 | ||||||
| chr8:53889646
|
G | A | 2 | a0001c0001t0002g0094a0001c0001t0002g0134 | 2 | HG00597.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.510+10044G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889646 | ||||||
| chr8:53889723
|
C | CTGTGTGT others(1): Show |
6 | a0001c0001t0011g0208a0001c0002t0002g0002a0001c0002t0002g0004others(3): Show | 6 | HG02109.hp1 HG02559.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+10148_510+1015 others(12): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889723 | |||||
| chr8:53889723
|
CTG | C | 172 | a0001c0001t0001g0018a0001c0001t0001g0031a0001c0001t0001g0035others(169): Show | 172 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.510+10154_510+1015 others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889723 | |||||
| chr8:53889723
|
CTGTG | C | 25 | a0001c0001t0001g0010a0001c0001t0001g0071a0001c0001t0001g0096others(22): Show | 25 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.510+10152_510+1015 others(8): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889723 | |||||
| chr8:53889723
|
CTGTGTG | C | 13 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0016others(10): Show | 13 | HG01069.hp2 HG01167.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.510+10150_510+1015 others(10): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889723 | |||||
| chr8:53889771
|
TCTC | T | 3 | a0001c0001t0002g0038a0001c0001t0004g0037a0001c0001t0008g0039 | 3 | HG01167.hp1 HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.510+10170_510+1017 others(7): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889771 | ||||||
| chr8:53889818
|
T | G | 1 | a0001c0001t0002g0073 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.510+10216T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889818 | ||||||
| chr8:53889850
|
G | T | 9 | a0001c0001t0001g0018a0001c0001t0001g0130a0001c0001t0001g0138others(6): Show | 9 | HG00408.hp2 HG00621.hp2 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.510+10248G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889850 | ||||||
| chr8:53889880
|
C | T | 2 | a0001c0001t0002g0021a0001c0001t0003g0030 | 2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.510+10278C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889880 | ||||||
| chr8:53889997
|
G | A | 1 | a0001c0001t0002g0245 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.510+10395G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889997 | ||||||
| chr8:53890216
|
T | G | 9 | a0001c0001t0002g0021a0001c0001t0003g0030a0001c0001t0011g0208others(6): Show | 9 | HG02109.hp1 HG02559.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.510+10614T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53890216 | ||||||
| chr8:53890220
|
C | T | 1 | a0001c0001t0002g0149 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.510+10618C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53890220 | ||||||
| chr8:53890354
|
A | G | 1 | a0001c0001t0003g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.510+10752A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53890354 | ||||||
| chr8:53890971
|
G | A | 6 | a0001c0001t0001g0180a0001c0001t0001g0201a0001c0001t0002g0019others(3): Show | 6 | NA18946.hp2 NA18952.hp1 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.510+11369G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53890971 | ||||||
| chr8:53891560
|
G | T | 47 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0001g0071others(44): Show | 47 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.510+11958G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53891560 | ||||||
| chr8:53891732
|
T | C | 2 | a0001c0001t0002g0021a0001c0001t0003g0030 | 2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.510+12130T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53891732 | ||||||
| chr8:53891888
|
T | A | 4 | a0001c0001t0002g0145a0001c0001t0002g0150a0001c0001t0002g0159others(1): Show | 4 | HG00140.hp2 HG01123.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+12286T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53891888 | ||||||
| chr8:53892242
|
A | G | 1 | a0001c0001t0003g0170 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.510+12640A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53892242 | ||||||
| chr8:53892307
|
T | C | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.510+12705T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53892307 | ||||||
| chr8:53892489
|
T | C | 2 | a0001c0001t0002g0021a0001c0001t0003g0030 | 2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.510+12887T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53892489 | ||||||
| chr8:53892595
|
A | T | 1 | a0001c0001t0002g0236 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.510+12993A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53892595 | ||||||
| chr8:53892652
|
T | C | 7 | a0001c0001t0011g0208a0001c0002t0001g0005a0001c0002t0002g0002others(4): Show | 7 | HG02109.hp1 HG02559.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+13050T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53892652 | ||||||
| chr8:53892919
|
A | G | 2 | a0001c0001t0002g0021a0001c0001t0003g0030 | 2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.510+13317A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53892919 | ||||||
| chr8:53892983
|
C | T | 41 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0064others(38): Show | 41 | HG01192.hp2 HG01243.hp2 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.510+13381C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53892983 | ||||||
| chr8:53893013
|
G | A | 8 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 8 | HG02055.hp2 HG02886.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.510+13411G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53893013 | ||||||
| chr8:53893079
|
A | G | 2 | a0001c0001t0001g0054a0001c0001t0001g0091 | 2 | HG02027.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.510+13477A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53893079 | ||||||
| chr8:53893475
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.510+13873G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53893475 | ||||||
| chr8:53893621
|
A | G | 65 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(62): Show | 65 | HG01069.hp2 HG01167.hp1 HG01192.hp2 others(62): Show |
intron_variant | MODIFIER | c.510+14019A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53893621 | ||||||
| chr8:53893822
|
T | G | 1 | a0001c0001t0002g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.510+14220T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53893822 | ||||||
| chr8:53893883
|
G | A | 1 | a0001c0002t0001g0005 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.510+14281G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53893883 | ||||||
| chr8:53893898
|
G | A | 1 | a0001c0001t0010g0188 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.510+14296G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53893898 | ||||||
| chr8:53893968
|
T | C | 2 | a0001c0001t0001g0081a0001c0001t0001g0085 | 2 | NA18955.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.510+14366T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53893968 | ||||||
| chr8:53893993
|
GA | G | 44 | a0001c0001t0001g0031a0001c0001t0001g0035a0001c0001t0001g0036others(41): Show | 44 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.510+14395delA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53893993 | |||||
| chr8:53894075
|
T | C | 2 | a0001c0001t0002g0021a0001c0001t0003g0030 | 2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.510+14473T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53894075 | ||||||
| chr8:53894206
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.510+14604A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53894206 | ||||||
| chr8:53894222
|
A | G | 38 | a0001c0001t0001g0052a0001c0001t0001g0064a0001c0001t0001g0074others(35): Show | 38 | HG01192.hp2 HG01243.hp2 HG01496.hp2 others(35): Show |
intron_variant | MODIFIER | c.510+14620A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53894222 | ||||||
| chr8:53894402
|
T | C | 65 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(62): Show | 65 | HG01069.hp2 HG01167.hp1 HG01192.hp2 others(62): Show |
intron_variant | MODIFIER | c.510+14800T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53894402 | ||||||
| chr8:53894488
|
C | A | 51 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0064others(48): Show | 51 | HG01192.hp2 HG01243.hp2 HG01496.hp2 others(48): Show |
intron_variant | MODIFIER | c.510+14886C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53894488 | ||||||
| chr8:53894488
|
C | T | 1 | a0001c0001t0002g0216 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.510+14886C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53894488 | ||||||
| chr8:53894624
|
A | G | 65 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(62): Show | 65 | HG01069.hp2 HG01167.hp1 HG01192.hp2 others(62): Show |
intron_variant | MODIFIER | c.510+15022A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53894624 | ||||||
| chr8:53894729
|
A | G | 5 | a0001c0001t0001g0143a0001c0001t0005g0118a0001c0001t0005g0119others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+15127A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53894729 | ||||||
| chr8:53894988
|
A | G | 1 | a0001c0005t0002g0113 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.510+15386A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53894988 | ||||||
| chr8:53895016
|
A | G | 1 | a0001c0001t0002g0179 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.510+15414A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53895016 | ||||||
| chr8:53895072
|
A | G | 1 | a0001c0001t0001g0115 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.510+15470A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53895072 | ||||||
| chr8:53895127
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.510+15525G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53895127 | ||||||
| chr8:53895203
|
T | C | 1 | a0001c0001t0001g0256 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.510+15601T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53895203 | ||||||
| chr8:53895558
|
A | G | 50 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0064others(47): Show | 50 | HG01192.hp2 HG01243.hp2 HG01496.hp2 others(47): Show |
intron_variant | MODIFIER | c.510+15956A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53895558 | ||||||
| chr8:53895594
|
C | T | 41 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0064others(38): Show | 41 | HG01192.hp2 HG01243.hp2 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.510+15992C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53895594 | ||||||
| chr8:53895713
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.510+16111C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53895713 | ||||||
| chr8:53895938
|
C | T | 1 | a0001c0003t0002g0029 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.510+16336C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53895938 | ||||||
| chr8:53895988
|
G | C | 256 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(253): Show | 256 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.510+16386G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53895988 | ||||||
| chr8:53896246
|
C | T | 50 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0064others(47): Show | 50 | HG01192.hp2 HG01243.hp2 HG01496.hp2 others(47): Show |
intron_variant | MODIFIER | c.510+16644C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53896246 | ||||||
| chr8:53896283
|
C | A | 1 | a0001c0001t0002g0185 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.510+16681C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53896283 | ||||||
| chr8:53896679
|
A | C | 2 | a0001c0001t0001g0036a0001c0001t0001g0067 | 2 | NA18954.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.510+17077A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53896679 | ||||||
| chr8:53897214
|
C | G | 50 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0064others(47): Show | 50 | HG01192.hp2 HG01243.hp2 HG01496.hp2 others(47): Show |
intron_variant | MODIFIER | c.510+17612C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53897214 | ||||||
| chr8:53897432
|
C | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.510+17830C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53897432 | ||||||
| chr8:53897495
|
C | A | 3 | a0001c0001t0002g0038a0001c0001t0004g0037a0001c0001t0008g0039 | 3 | HG01167.hp1 HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.510+17893C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53897495 | ||||||
| chr8:53897519
|
A | G | 50 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0064others(47): Show | 50 | HG01192.hp2 HG01243.hp2 HG01496.hp2 others(47): Show |
intron_variant | MODIFIER | c.510+17917A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53897519 | ||||||
| chr8:53897607
|
T | C | 65 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(62): Show | 65 | HG01069.hp2 HG01167.hp1 HG01192.hp2 others(62): Show |
intron_variant | MODIFIER | c.510+18005T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53897607 | ||||||
| chr8:53897890
|
G | A | 41 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0064others(38): Show | 41 | HG01192.hp2 HG01243.hp2 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.510+18288G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53897890 | ||||||
| chr8:53897891
|
C | T | 50 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0064others(47): Show | 50 | HG01192.hp2 HG01243.hp2 HG01496.hp2 others(47): Show |
intron_variant | MODIFIER | c.510+18289C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53897891 | ||||||
| chr8:53897921
|
G | A | 1 | a0001c0001t0002g0172 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.510+18319G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53897921 | ||||||
| chr8:53898033
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.510+18431C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53898033 | ||||||
| chr8:53898101
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.510+18499G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53898101 | ||||||
| chr8:53898101
|
G | C | 15 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(12): Show | 15 | HG01069.hp2 HG01167.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.510+18499G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53898101 | ||||||
| chr8:53898104
|
C | T | 1 | a0001c0001t0002g0242 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.510+18502C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53898104 | ||||||
| chr8:53898111
|
C | T | 2 | a0001c0001t0002g0021a0001c0001t0003g0030 | 2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.510+18509C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53898111 | ||||||
| chr8:53898132
|
T | C | 1 | a0001c0001t0001g0082 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.510+18530T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53898132 | ||||||
| chr8:53898373
|
T | A | 41 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0064others(38): Show | 41 | HG01192.hp2 HG01243.hp2 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.510+18771T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53898373 | ||||||
| chr8:53898631
|
A | G | 7 | a0001c0001t0011g0208a0001c0002t0001g0005a0001c0002t0002g0002others(4): Show | 7 | HG02109.hp1 HG02559.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+19029A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53898631 | ||||||
| chr8:53898828
|
G | A | 65 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(62): Show | 65 | HG01069.hp2 HG01167.hp1 HG01192.hp2 others(62): Show |
intron_variant | MODIFIER | c.510+19226G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53898828 | ||||||
| chr8:53899092
|
C | T | 2 | a0001c0001t0006g0043a0001c0001t0006g0044 | 2 | HG01069.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.510+19490C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53899092 | ||||||
| chr8:53899093
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.510+19491C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53899093 | ||||||
| chr8:53899307
|
G | A | 1 | a0001c0001t0003g0237 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.510+19705G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53899307 | ||||||
| chr8:53899388
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.510+19786G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53899388 | ||||||
| chr8:53899766
|
A | G | 11 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(8): Show | 11 | HG01167.hp1 HG02055.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.510+20164A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53899766 | ||||||
| chr8:53899819
|
G | C | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.510+20217G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53899819 | ||||||
| chr8:53899861
|
A | T | 1 | a0001c0001t0002g0017 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.510+20259A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53899861 | ||||||
| chr8:53899908
|
C | T | 64 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0064others(61): Show | 64 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(61): Show |
intron_variant | MODIFIER | c.510+20306C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53899908 | ||||||
| chr8:53900028
|
C | T | 1 | a0001c0001t0002g0124 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.510+20426C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53900028 | ||||||
| chr8:53900152
|
A | G | 2 | a0001c0001t0001g0093a0001c0001t0001g0105 | 2 | NA18961.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.510+20550A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53900152 | ||||||
| chr8:53900234
|
TG | T | 3 | a0001c0001t0001g0023a0001c0001t0003g0022a0001c0001t0003g0024 | 3 | HG02886.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.510+20635delG | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53900234 | |||||
| chr8:53900254
|
A | G | 12 | a0001c0001t0002g0020a0001c0001t0002g0169a0001c0001t0002g0232others(9): Show | 12 | HG00741.hp1 HG01109.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.510+20652A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53900254 | ||||||
| chr8:53900799
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.510+21197T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53900799 | ||||||
| chr8:53900887
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.510+21285C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53900887 | ||||||
| chr8:53900889
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.510+21287C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53900889 | ||||||
| chr8:53900985
|
A | G | 70 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(67): Show | 70 | HG01069.hp2 HG01167.hp1 HG01192.hp2 others(67): Show |
intron_variant | MODIFIER | c.510+21383A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53900985 | ||||||
| chr8:53901062
|
C | CT | 6 | a0001c0001t0001g0018a0001c0001t0001g0225a0001c0001t0001g0230others(3): Show | 6 | HG01069.hp2 HG02074.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.510+21479dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53901062 | |||||
| chr8:53901062
|
CT | C | 51 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0064others(48): Show | 51 | HG01071.hp2 HG01167.hp2 HG01192.hp2 others(48): Show |
intron_variant | MODIFIER | c.510+21479delT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53901062 | |||||
| chr8:53901062
|
CTT | C | 5 | a0001c0001t0001g0077a0001c0001t0001g0081a0001c0001t0002g0021others(2): Show | 5 | HG01070.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.510+21478_510+2147 others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53901062 | |||||
| chr8:53901193
|
G | A | 4 | a0001c0001t0005g0118a0001c0001t0005g0119a0001c0001t0007g0033others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+21591G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53901193 | ||||||
| chr8:53901360
|
G | A | 2 | a0001c0001t0006g0043a0001c0001t0006g0044 | 2 | HG01069.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.510+21758G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53901360 | ||||||
| chr8:53901547
|
T | A | 2 | a0001c0001t0005g0118a0001c0001t0005g0119 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.510+21945T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53901547 | ||||||
| chr8:53901614
|
A | T | 17 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(14): Show | 17 | HG01069.hp2 HG01167.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.510+22012A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53901614 | ||||||
| chr8:53901719
|
C | T | 1 | a0001c0001t0001g0256 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.510+22117C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53901719 | ||||||
| chr8:53901725
|
T | C | 2 | a0001c0001t0001g0116a0001c0001t0001g0202 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.510+22123T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53901725 | ||||||
| chr8:53901821
|
G | GCACTC | 4 | a0001c0001t0002g0021a0001c0001t0003g0030a0001c0001t0005g0118others(1): Show | 4 | HG02055.hp1 HG02630.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+22224_510+2222 others(9): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53901821 | |||||
| chr8:53901870
|
A | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0061 | 2 | HG02698.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.510+22268A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53901870 | ||||||
| chr8:53902081
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.510+22479G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902081 | ||||||
| chr8:53902104
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.510+22502G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902104 | ||||||
| chr8:53902246
|
C | T | 1 | a0001c0003t0002g0029 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.510+22644C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902246 | ||||||
| chr8:53902252
|
G | C | 1 | a0001c0001t0002g0217 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.510+22650G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902252 | ||||||
| chr8:53902385
|
A | G | 79 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0023others(76): Show | 79 | HG00741.hp1 HG01069.hp2 HG01167.hp1 others(76): Show |
intron_variant | MODIFIER | c.510+22783A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902385 | ||||||
| chr8:53902443
|
A | G | 24 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(21): Show | 24 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.510+22841A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902443 | ||||||
| chr8:53902526
|
A | G | 6 | a0001c0001t0002g0021a0001c0001t0002g0244a0001c0001t0003g0030others(3): Show | 6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+22924A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902526 | ||||||
| chr8:53902562
|
C | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.510+22960C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902562 | ||||||
| chr8:53902575
|
A | G | 24 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(21): Show | 24 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.510+22973A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902575 | ||||||
| chr8:53902631
|
T | C | 1 | a0001c0001t0002g0155 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.510+23029T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902631 | ||||||
| chr8:53902731
|
C | CT | 62 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(59): Show | 62 | HG00741.hp1 HG01192.hp2 HG01243.hp2 others(59): Show |
intron_variant | MODIFIER | c.510+23140dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53902731 | |||||
| chr8:53902788
|
C | T | 1 | a0001c0001t0003g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.510+23186C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902788 | ||||||
| chr8:53902808
|
C | T | 3 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195 | 3 | HG01069.hp1 HG01071.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.510+23206C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902808 | ||||||
| chr8:53902818
|
C | T | 2 | a0001c0001t0002g0038a0001c0001t0004g0037 | 2 | HG01167.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.510+23216C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902818 | ||||||
| chr8:53902853
|
G | A | 55 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(52): Show | 55 | HG00741.hp1 HG01192.hp2 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.510+23251G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902853 | ||||||
| chr8:53902887
|
G | A | 6 | a0001c0001t0002g0021a0001c0001t0002g0244a0001c0001t0003g0030others(3): Show | 6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+23285G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902887 | ||||||
| chr8:53902960
|
G | A | 55 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(52): Show | 55 | HG00741.hp1 HG01192.hp2 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.510+23358G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902960 | ||||||
| chr8:53902979
|
A | G | 79 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0023others(76): Show | 79 | HG00741.hp1 HG01069.hp2 HG01167.hp1 others(76): Show |
intron_variant | MODIFIER | c.510+23377A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902979 | ||||||
| chr8:53903018
|
T | C | 256 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(253): Show | 256 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.510+23416T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53903018 | ||||||
| chr8:53903241
|
T | C | 79 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0023others(76): Show | 79 | HG00741.hp1 HG01069.hp2 HG01167.hp1 others(76): Show |
intron_variant | MODIFIER | c.510+23639T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53903241 | ||||||
| chr8:53903269
|
G | A | 79 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0023others(76): Show | 79 | HG00741.hp1 HG01069.hp2 HG01167.hp1 others(76): Show |
intron_variant | MODIFIER | c.510+23667G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53903269 | ||||||
| chr8:53903883
|
G | A | 6 | a0001c0001t0002g0021a0001c0001t0002g0244a0001c0001t0003g0030others(3): Show | 6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+24281G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53903883 | ||||||
| chr8:53903884
|
C | T | 1 | a0001c0001t0008g0114 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.510+24282C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53903884 | ||||||
| chr8:53903938
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.510+24336G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53903938 | ||||||
| chr8:53904011
|
T | C | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.510+24409T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53904011 | ||||||
| chr8:53904018
|
G | A | 4 | a0001c0001t0002g0244a0001c0003t0001g0028a0001c0003t0003g0026others(1): Show | 4 | HG02280.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+24416G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53904018 | ||||||
| chr8:53904061
|
A | G | 18 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(15): Show | 18 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.510+24459A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53904061 | ||||||
| chr8:53904126
|
CT | C | 5 | a0001c0001t0001g0080a0001c0001t0001g0197a0001c0001t0002g0169others(2): Show | 5 | HG01168.hp2 HG02132.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.510+24540delT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53904126 | |||||
| chr8:53904126
|
CTT | C | 6 | a0001c0001t0002g0021a0001c0001t0002g0244a0001c0001t0003g0030others(3): Show | 6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+24539_510+2454 others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53904126 | |||||
| chr8:53904126
|
CTTT | C | 18 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(15): Show | 18 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.510+24538_510+2454 others(7): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53904126 | |||||
| chr8:53904352
|
G | A | 2 | a0001c0001t0005g0118a0001c0001t0005g0119 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.510+24750G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53904352 | ||||||
| chr8:53904424
|
A | G | 24 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(21): Show | 24 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.510+24822A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53904424 | ||||||
| chr8:53904589
|
T | C | 1 | a0001c0001t0002g0034 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.510+24987T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53904589 | ||||||
| chr8:53904599
|
T | C | 24 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(21): Show | 24 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.510+24997T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53904599 | ||||||
| chr8:53904763
|
TAATA | T | 17 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(14): Show | 17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.510+25164_510+2516 others(8): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53904763 | |||||
| chr8:53904863
|
T | G | 24 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(21): Show | 24 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.510+25261T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53904863 | ||||||
| chr8:53904971
|
A | G | 4 | a0001c0001t0002g0032a0001c0001t0002g0038a0001c0001t0004g0037others(1): Show | 4 | HG01167.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+25369A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53904971 | ||||||
| chr8:53905026
|
C | T | 6 | a0001c0001t0002g0021a0001c0001t0002g0244a0001c0001t0003g0030others(3): Show | 6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+25424C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53905026 | ||||||
| chr8:53905188
|
T | C | 55 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(52): Show | 55 | HG00741.hp1 HG01192.hp2 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.510+25586T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53905188 | ||||||
| chr8:53905231
|
A | G | 4 | a0001c0001t0002g0032a0001c0001t0002g0038a0001c0001t0004g0037others(1): Show | 4 | HG01167.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+25629A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53905231 | ||||||
| chr8:53905886
|
C | G | 1 | a0001c0001t0002g0224 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.510+26284C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53905886 | ||||||
| chr8:53905997
|
G | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.510+26395G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53905997 | ||||||
| chr8:53906024
|
G | A | 6 | a0001c0001t0002g0021a0001c0001t0002g0244a0001c0001t0003g0030others(3): Show | 6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+26422G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53906024 | ||||||
| chr8:53906077
|
C | T | 4 | a0001c0001t0005g0118a0001c0001t0005g0119a0001c0001t0006g0043others(1): Show | 4 | HG01069.hp2 HG02055.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+26475C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53906077 | ||||||
| chr8:53906172
|
T | C | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.510+26570T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53906172 | ||||||
| chr8:53906213
|
A | G | 23 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(20): Show | 23 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.510+26611A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53906213 | ||||||
| chr8:53906259
|
C | T | 1 | a0001c0001t0003g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.510+26657C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53906259 | ||||||
| chr8:53906425
|
G | A | 4 | a0001c0001t0002g0032a0001c0001t0002g0038a0001c0001t0004g0037others(1): Show | 4 | HG01167.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+26823G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53906425 | ||||||
| chr8:53906431
|
C | A | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.510+26829C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53906431 | ||||||
| chr8:53906442
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.510+26840T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53906442 | ||||||
| chr8:53906737
|
T | C | 23 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(20): Show | 23 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.510+27135T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53906737 | ||||||
| chr8:53906773
|
A | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.510+27171A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53906773 | ||||||
| chr8:53906793
|
C | G | 17 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(14): Show | 17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.510+27191C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53906793 | ||||||
| chr8:53907181
|
C | T | 1 | a0001c0001t0002g0034 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.510+27579C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53907181 | ||||||
| chr8:53907229
|
C | T | 4 | a0001c0001t0002g0244a0001c0003t0001g0028a0001c0003t0003g0026others(1): Show | 4 | HG02280.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+27627C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53907229 | ||||||
| chr8:53907240
|
T | C | 17 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(14): Show | 17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.510+27638T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53907240 | ||||||
| chr8:53907353
|
G | A | 17 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(14): Show | 17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.510+27751G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53907353 | ||||||
| chr8:53907413
|
G | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.510+27811G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53907413 | ||||||
| chr8:53907509
|
A | G | 6 | a0001c0001t0002g0021a0001c0001t0002g0244a0001c0001t0003g0030others(3): Show | 6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+27907A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53907509 | ||||||
| chr8:53907587
|
G | GA | 31 | a0001c0001t0002g0020a0001c0001t0002g0108a0001c0001t0002g0117others(28): Show | 31 | HG01109.hp2 HG01192.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.510+27996dupA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53907587 | |||||
| chr8:53907587
|
G | GAA | 6 | a0001c0001t0002g0021a0001c0001t0002g0244a0001c0001t0003g0030others(3): Show | 6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+27995_510+2799 others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53907587 | |||||
| chr8:53907702
|
G | GCTAA | 5 | a0001c0001t0002g0244a0001c0001t0003g0030a0001c0003t0001g0028others(2): Show | 5 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+28102_510+2810 others(8): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53907702 | |||||
| chr8:53907722
|
C | T | 1 | a0001c0002t0003g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.510+28120C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53907722 | ||||||
| chr8:53907742
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.510+28140G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53907742 | ||||||
| chr8:53907841
|
C | T | 1 | a0001c0001t0003g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.510+28239C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53907841 | ||||||
| chr8:53907889
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.510+28287T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53907889 | ||||||
| chr8:53907955
|
G | GA | 6 | a0001c0001t0002g0021a0001c0001t0002g0244a0001c0001t0003g0030others(3): Show | 6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+28359dupA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53907955 | |||||
| chr8:53907965
|
A | G | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.510+28363A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53907965 | ||||||
| chr8:53908184
|
G | C | 1 | a0001c0001t0002g0258 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.510+28582G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53908184 | ||||||
| chr8:53908259
|
G | C | 4 | a0001c0001t0002g0032a0001c0001t0002g0038a0001c0001t0004g0037others(1): Show | 4 | HG01167.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+28657G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53908259 | ||||||
| chr8:53908298
|
T | C | 23 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(20): Show | 23 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.510+28696T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53908298 | ||||||
| chr8:53908404
|
C | G | 2 | a0001c0001t0001g0092a0001c0001t0001g0098 | 2 | NA18975.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.510+28802C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53908404 | ||||||
| chr8:53908513
|
G | A | 17 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(14): Show | 17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.510+28911G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53908513 | ||||||
| chr8:53908632
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0123 | 2 | NA18945.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.510+29030C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53908632 | ||||||
| chr8:53908640
|
C | CA | 110 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(107): Show | 110 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.510+29051dupA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53908640 | |||||
| chr8:53909203
|
ATG | A | 4 | a0001c0001t0002g0171a0001c0001t0002g0191a0001c0001t0002g0203others(1): Show | 4 | HG01192.hp2 HG03540.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+29607_510+2960 others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909203 | |||||
| chr8:53909207
|
G | GTGTGTA | 5 | a0001c0001t0001g0015a0001c0001t0002g0016a0001c0001t0005g0118others(2): Show | 5 | HG02055.hp1 HG02055.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.510+29608_510+2960 others(10): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909207 | |||||
| chr8:53909207
|
GTGTA | G | 11 | a0001c0001t0001g0121a0001c0001t0001g0166a0001c0001t0001g0184others(8): Show | 11 | HG02027.hp1 HG02083.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.510+29607_510+2961 others(8): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909207 | |||||
| chr8:53909207
|
GTGTATA | G | 20 | a0001c0001t0001g0081a0001c0001t0002g0020a0001c0001t0002g0146others(17): Show | 20 | HG00140.hp2 HG01109.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.510+29607_510+2961 others(10): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909207 | |||||
| chr8:53909207
|
GTGTATAT others(1): Show |
G | 27 | a0001c0001t0001g0054a0001c0001t0001g0060a0001c0001t0001g0075others(24): Show | 27 | HG00741.hp1 HG01123.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.510+29607_510+2961 others(12): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909207 | |||||
| chr8:53909207
|
GTGTATAT others(3): Show |
G | 36 | a0001c0001t0001g0055a0001c0001t0001g0064a0001c0001t0001g0071others(33): Show | 36 | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.510+29607_510+2961 others(14): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909207 | |||||
| chr8:53909207
|
GTGTATAT others(5): Show |
G | 7 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0080others(4): Show | 7 | HG01243.hp2 HG02132.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+29607_510+2961 others(16): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909207 | |||||
| chr8:53909207
|
GTGTATAT others(21): Show |
G | 1 | a0001c0001t0002g0134 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.510+29607_510+2963 others(32): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909207 | |||||
| chr8:53909207
|
GTGTATAT others(23): Show |
G | 4 | a0001c0001t0002g0244a0001c0003t0001g0028a0001c0003t0003g0026others(1): Show | 4 | HG02280.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+29607_510+2963 others(34): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909207 | |||||
| chr8:53909207
|
GTGTATAT others(25): Show |
G | 2 | a0001c0001t0002g0021a0001c0001t0003g0030 | 2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.510+29607_510+2963 others(36): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909207 | |||||
| chr8:53909209
|
G | A | 5 | a0001c0001t0001g0068a0001c0001t0001g0156a0001c0001t0002g0159others(2): Show | 5 | HG01346.hp1 HG02165.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.510+29607G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909209 | ||||||
| chr8:53909209
|
G | GTA | 12 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0093others(9): Show | 12 | HG01069.hp1 HG01071.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.510+29652_510+2965 others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909209 | |||||
| chr8:53909209
|
G | GTGTA | 6 | a0001c0001t0001g0010a0001c0001t0002g0246a0001c0001t0004g0011others(3): Show | 6 | HG01069.hp2 HG02486.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.510+29608_510+2960 others(8): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909209 | |||||
| chr8:53909209
|
G | GTGTATGT others(3): Show |
1 | a0001c0001t0001g0143 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.510+29608_510+2960 others(14): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909209 | |||||
| chr8:53909209
|
GTA | G | 45 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0035others(42): Show | 45 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.510+29652_510+2965 others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909209 | |||||
| chr8:53909209
|
GTATA | G | 18 | a0001c0001t0001g0092a0001c0001t0001g0101a0001c0001t0001g0112others(15): Show | 18 | HG00140.hp1 HG00323.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.510+29650_510+2965 others(8): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909209 | |||||
| chr8:53909209
|
GTATATA | G | 19 | a0001c0001t0001g0018a0001c0001t0001g0058a0001c0001t0001g0095others(16): Show | 19 | HG00408.hp2 HG00438.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.510+29648_510+2965 others(10): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909209 | |||||
| chr8:53909209
|
GTATATAT others(3): Show |
G | 1 | a0001c0001t0007g0033 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.510+29644_510+2965 others(14): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909209 | |||||
| chr8:53909209
|
GTATATAT others(5): Show |
G | 1 | a0001c0001t0007g0045 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.510+29642_510+2965 others(16): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909209 | |||||
| chr8:53909209
|
GTATATAT others(7): Show |
G | 4 | a0001c0001t0001g0042a0001c0001t0001g0105a0001c0001t0001g0201others(1): Show | 4 | HG03688.hp2 NA18988.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+29640_510+2965 others(18): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909209 | |||||
| chr8:53909209
|
GTATATAT others(11): Show |
G | 2 | a0001c0001t0009g0136a0001c0003t0002g0029 | 2 | HG02886.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.510+29636_510+2965 others(22): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909209 | |||||
| chr8:53909209
|
GTATATAT others(13): Show |
G | 1 | a0001c0001t0001g0187 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.510+29634_510+2965 others(24): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909209 | |||||
| chr8:53909209
|
GTATATAT others(15): Show |
G | 1 | a0001c0001t0001g0084 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.510+29632_510+2965 others(26): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909209 | |||||
| chr8:53909209
|
GTATATAT others(19): Show |
G | 2 | a0001c0001t0002g0243a0001c0001t0002g0245 | 2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.510+29628_510+2965 others(30): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909209 | |||||
| chr8:53909211
|
A | G | 8 | a0001c0001t0001g0010a0001c0001t0002g0246a0001c0001t0004g0011others(5): Show | 8 | HG01069.hp2 HG02055.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.510+29609A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909211 | ||||||
| chr8:53909213
|
A | G | 5 | a0001c0001t0002g0032a0001c0001t0002g0038a0001c0001t0002g0248others(2): Show | 5 | HG01074.hp2 HG01167.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.510+29611A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909213 | ||||||
| chr8:53909217
|
A | G | 4 | a0001c0001t0002g0032a0001c0001t0002g0038a0001c0001t0004g0037others(1): Show | 4 | HG01167.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+29615A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909217 | ||||||
| chr8:53909229
|
A | G | 1 | a0001c0003t0002g0029 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.510+29627A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909229 | ||||||
| chr8:53909233
|
A | G | 1 | a0001c0003t0002g0029 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.510+29631A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909233 | ||||||
| chr8:53909254
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.510+29652T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909254 | ||||||
| chr8:53909255
|
A | C | 1 | a0001c0001t0001g0048 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.510+29653A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909255 | ||||||
| chr8:53909256
|
C | T | 1 | a0001c0001t0001g0048 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.510+29654C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909256 | ||||||
| chr8:53909302
|
A | T | 23 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(20): Show | 23 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.510+29700A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909302 | ||||||
| chr8:53909347
|
T | C | 1 | a0001c0001t0002g0131 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.510+29745T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909347 | ||||||
| chr8:53909428
|
T | G | 1 | a0001c0003t0002g0029 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.510+29826T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909428 | ||||||
| chr8:53909445
|
T | C | 23 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(20): Show | 23 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.510+29843T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909445 | ||||||
| chr8:53909456
|
A | G | 23 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(20): Show | 23 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.510+29854A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909456 | ||||||
| chr8:53909530
|
AG | A | 4 | a0001c0001t0002g0032a0001c0001t0002g0038a0001c0001t0004g0037others(1): Show | 4 | HG01167.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+29929delG | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909530 | ||||||
| chr8:53909554
|
C | T | 15 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(12): Show | 15 | HG01069.hp2 HG01167.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.510+29952C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909554 | ||||||
| chr8:53909577
|
C | G | 17 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(14): Show | 17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.510+29975C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909577 | ||||||
| chr8:53909600
|
T | C | 2 | a0001c0001t0006g0043a0001c0001t0006g0044 | 2 | HG01069.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.511-29976T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909600 | ||||||
| chr8:53909616
|
T | G | 17 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(14): Show | 17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-29960T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909616 | ||||||
| chr8:53909759
|
G | A | 134 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0023others(131): Show | 134 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.511-29817G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909759 | ||||||
| chr8:53910277
|
CA | C | 6 | a0001c0001t0002g0021a0001c0001t0002g0244a0001c0001t0003g0030others(3): Show | 6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-29291delA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53910277 | |||||
| chr8:53910421
|
GA | G | 110 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(107): Show | 110 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.511-29145delA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53910421 | |||||
| chr8:53910422
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0003t0004g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.511-29153_511-2914 others(14): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53910422 | ||||||
| chr8:53910469
|
T | C | 6 | a0001c0001t0002g0021a0001c0001t0002g0244a0001c0001t0003g0030others(3): Show | 6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-29107T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53910469 | ||||||
| chr8:53910505
|
A | C | 9 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(6): Show | 9 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.511-29071A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53910505 | ||||||
| chr8:53910507
|
G | T | 1 | a0001c0001t0002g0124 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.511-29069G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53910507 | ||||||
| chr8:53910666
|
C | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.511-28910C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53910666 | ||||||
| chr8:53910748
|
G | A | 134 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0023others(131): Show | 134 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.511-28828G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53910748 | ||||||
| chr8:53910873
|
A | G | 4 | a0001c0001t0002g0032a0001c0001t0002g0038a0001c0001t0004g0037others(1): Show | 4 | HG01167.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-28703A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53910873 | ||||||
| chr8:53911215
|
C | G | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.511-28361C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53911215 | ||||||
| chr8:53911241
|
G | C | 23 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(20): Show | 23 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.511-28335G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53911241 | ||||||
| chr8:53911330
|
C | A | 1 | a0001c0001t0002g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.511-28246C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53911330 | ||||||
| chr8:53911413
|
G | A | 36 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(33): Show | 36 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.511-28163G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53911413 | ||||||
| chr8:53911459
|
T | A | 1 | a0001c0001t0002g0226 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.511-28117T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53911459 | ||||||
| chr8:53911503
|
C | T | 23 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(20): Show | 23 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.511-28073C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53911503 | ||||||
| chr8:53911562
|
T | TTG | 134 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0023others(131): Show | 134 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.511-28014_511-2801 others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53911562 | ||||||
| chr8:53911594
|
G | A | 17 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(14): Show | 17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-27982G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53911594 | ||||||
| chr8:53911606
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.511-27970G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53911606 | ||||||
| chr8:53911619
|
G | A | 1 | a0001c0001t0002g0106 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.511-27957G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53911619 | ||||||
| chr8:53911732
|
G | A | 1 | a0001c0001t0002g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.511-27844G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53911732 | ||||||
| chr8:53912144
|
A | G | 2 | a0001c0001t0001g0068a0001c0001t0001g0256 | 2 | NA18612.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.511-27432A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53912144 | ||||||
| chr8:53912234
|
A | G | 2 | a0001c0001t0001g0023a0001c0001t0003g0024 | 2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.511-27342A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53912234 | ||||||
| chr8:53912352
|
A | AT | 17 | a0001c0001t0001g0010a0001c0001t0001g0142a0001c0001t0001g0143others(14): Show | 17 | HG01069.hp2 HG01167.hp1 HG02273.hp2 others(14): Show |
intron_variant | MODIFIER | c.511-27207dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53912352 | |||||
| chr8:53912352
|
AT | A | 167 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0035others(164): Show | 167 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.511-27207delT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53912352 | |||||
| chr8:53912575
|
A | G | 6 | a0001c0001t0002g0021a0001c0001t0002g0244a0001c0001t0003g0030others(3): Show | 6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-27001A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53912575 | ||||||
| chr8:53912595
|
C | T | 110 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(107): Show | 110 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.511-26981C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53912595 | ||||||
| chr8:53912970
|
A | AT | 5 | a0001c0001t0001g0015a0001c0001t0002g0151a0001c0001t0002g0226others(2): Show | 5 | HG02055.hp2 HG02559.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.511-26593dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53912970 | |||||
| chr8:53913352
|
G | A | 110 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(107): Show | 110 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.511-26224G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53913352 | ||||||
| chr8:53913352
|
G | T | 23 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(20): Show | 23 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.511-26224G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53913352 | ||||||
| chr8:53913403
|
G | A | 6 | a0001c0001t0002g0021a0001c0001t0002g0244a0001c0001t0003g0030others(3): Show | 6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-26173G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53913403 | ||||||
| chr8:53913577
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.511-25999G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53913577 | ||||||
| chr8:53913773
|
C | A | 17 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(14): Show | 17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-25803C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53913773 | ||||||
| chr8:53914037
|
C | CT | 17 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(14): Show | 17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-25528dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53914037 | |||||
| chr8:53914037
|
C | CTTTTTTT others(2): Show |
6 | a0001c0001t0002g0021a0001c0001t0002g0244a0001c0001t0003g0030others(3): Show | 6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-25536_511-2552 others(13): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53914037 | |||||
| chr8:53914037
|
C | CTTTTTTT others(3): Show |
7 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0001t0002g0169others(4): Show | 7 | HG02451.hp2 HG02602.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.511-25537_511-2552 others(14): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53914037 | |||||
| chr8:53914037
|
C | CTTTTTTT others(4): Show |
100 | a0001c0001t0001g0023a0001c0001t0001g0054a0001c0001t0001g0060others(97): Show | 100 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.511-25538_511-2552 others(15): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53914037 | |||||
| chr8:53914037
|
C | CTTTTTTT others(5): Show |
3 | a0001c0001t0001g0064a0001c0001t0001g0068a0001c0001t0001g0156 | 3 | HG02165.hp1 NA18612.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.511-25528_511-2552 others(16): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53914037 | |||||
| chr8:53914199
|
T | C | 1 | a0001c0001t0003g0234 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.511-25377T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53914199 | ||||||
| chr8:53914255
|
T | C | 40 | a0001c0001t0001g0052a0001c0001t0001g0054a0001c0001t0001g0064others(37): Show | 40 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.511-25321T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53914255 | ||||||
| chr8:53914285
|
C | T | 8 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(5): Show | 8 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.511-25291C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53914285 | ||||||
| chr8:53914344
|
G | A | 17 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(14): Show | 17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-25232G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53914344 | ||||||
| chr8:53914422
|
C | A | 2 | a0001c0001t0005g0118a0001c0001t0005g0119 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.511-25154C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53914422 | ||||||
| chr8:53914480
|
T | A | 1 | a0001c0001t0002g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.511-25096T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53914480 | ||||||
| chr8:53914557
|
A | G | 1 | a0001c0001t0002g0199 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.511-25019A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53914557 | ||||||
| chr8:53914599
|
G | A | 1 | a0001c0001t0002g0122 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.511-24977G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53914599 | ||||||
| chr8:53914783
|
C | T | 6 | a0001c0001t0002g0021a0001c0001t0002g0244a0001c0001t0003g0030others(3): Show | 6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-24793C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53914783 | ||||||
| chr8:53914841
|
A | T | 17 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(14): Show | 17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-24735A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53914841 | ||||||
| chr8:53914842
|
A | T | 136 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0023others(133): Show | 136 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.511-24734A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53914842 | ||||||
| chr8:53914872
|
C | T | 17 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(14): Show | 17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-24704C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53914872 | ||||||
| chr8:53914880
|
C | T | 36 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(33): Show | 36 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.511-24696C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53914880 | ||||||
| chr8:53914976
|
A | C | 42 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(39): Show | 42 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.511-24600A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53914976 | ||||||
| chr8:53915017
|
C | G | 6 | a0001c0001t0002g0021a0001c0001t0002g0244a0001c0001t0003g0030others(3): Show | 6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-24559C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53915017 | ||||||
| chr8:53915032
|
T | C | 42 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(39): Show | 42 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.511-24544T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53915032 | ||||||
| chr8:53915077
|
G | A | 1 | a0001c0001t0002g0157 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.511-24499G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53915077 | ||||||
| chr8:53915100
|
C | T | 17 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(14): Show | 17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-24476C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53915100 | ||||||
| chr8:53915116
|
G | C | 1 | a0001c0001t0002g0106 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.511-24460G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53915116 | ||||||
| chr8:53915144
|
C | CA | 132 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0052others(129): Show | 132 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.511-24417dupA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53915144 | |||||
| chr8:53915144
|
CA | C | 51 | a0001c0001t0001g0018a0001c0001t0001g0050a0001c0001t0001g0058others(48): Show | 51 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.511-24417delA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53915144 | |||||
| chr8:53915232
|
G | A | 1 | a0001c0001t0003g0051 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.511-24344G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53915232 | ||||||
| chr8:53915289
|
C | T | 2 | a0001c0001t0005g0118a0001c0001t0005g0119 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.511-24287C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53915289 | ||||||
| chr8:53915307
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.511-24269G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53915307 | ||||||
| chr8:53915347
|
G | A | 1 | a0001c0001t0002g0104 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.511-24229G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53915347 | ||||||
| chr8:53915378
|
T | C | 15 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(12): Show | 15 | HG01069.hp2 HG01167.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.511-24198T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53915378 | ||||||
| chr8:53915403
|
G | T | 42 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(39): Show | 42 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.511-24173G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53915403 | ||||||
| chr8:53915642
|
G | C | 59 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0023others(56): Show | 59 | HG00741.hp1 HG01069.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.511-23934G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53915642 | ||||||
| chr8:53915795
|
C | T | 42 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(39): Show | 42 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.511-23781C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53915795 | ||||||
| chr8:53915834
|
A | G | 36 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(33): Show | 36 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.511-23742A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53915834 | ||||||
| chr8:53915854
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.511-23722G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53915854 | ||||||
| chr8:53916037
|
A | T | 2 | a0001c0001t0006g0043a0001c0001t0006g0044 | 2 | HG01069.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.511-23539A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53916037 | ||||||
| chr8:53916158
|
G | A | 1 | a0001c0001t0002g0162 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.511-23418G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53916158 | ||||||
| chr8:53916427
|
A | AT | 10 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0096others(7): Show | 10 | HG00741.hp2 HG02155.hp2 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.511-23144dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53916427 | |||||
| chr8:53916763
|
C | T | 42 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(39): Show | 42 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.511-22813C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53916763 | ||||||
| chr8:53916949
|
C | G | 1 | a0001c0003t0003g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.511-22627C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53916949 | ||||||
| chr8:53917092
|
A | G | 74 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0001g0068others(71): Show | 74 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.511-22484A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917092 | ||||||
| chr8:53917122
|
C | G | 17 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(14): Show | 17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-22454C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917122 | ||||||
| chr8:53917139
|
T | TTTTTG | 33 | a0001c0001t0001g0052a0001c0001t0001g0054a0001c0001t0001g0064others(30): Show | 33 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(30): Show |
intron_variant | MODIFIER | c.511-22417_511-2241 others(9): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53917139 | |||||
| chr8:53917182
|
T | A | 1 | a0001c0001t0003g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.511-22394T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917182 | ||||||
| chr8:53917230
|
G | C | 134 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0023others(131): Show | 134 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.511-22346G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917230 | ||||||
| chr8:53917338
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.511-22238A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917338 | ||||||
| chr8:53917374
|
C | A | 2 | a0001c0001t0002g0150a0001c0001t0002g0172 | 2 | HG00140.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.511-22202C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917374 | ||||||
| chr8:53917440
|
T | C | 36 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(33): Show | 36 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.511-22136T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917440 | ||||||
| chr8:53917491
|
A | T | 36 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(33): Show | 36 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.511-22085A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917491 | ||||||
| chr8:53917512
|
T | C | 74 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0001g0068others(71): Show | 74 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.511-22064T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917512 | ||||||
| chr8:53917587
|
T | C | 2 | a0001c0001t0006g0043a0001c0001t0006g0044 | 2 | HG01069.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.511-21989T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917587 | ||||||
| chr8:53917719
|
C | T | 134 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0023others(131): Show | 134 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.511-21857C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917719 | ||||||
| chr8:53917720
|
T | G | 59 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0023others(56): Show | 59 | HG00741.hp1 HG01069.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.511-21856T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917720 | ||||||
| chr8:53917756
|
C | T | 74 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0001g0068others(71): Show | 74 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.511-21820C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917756 | ||||||
| chr8:53917805
|
A | G | 134 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0023others(131): Show | 134 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.511-21771A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917805 | ||||||
| chr8:53917851
|
A | C | 42 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(39): Show | 42 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.511-21725A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917851 | ||||||
| chr8:53917984
|
A | G | 42 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(39): Show | 42 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.511-21592A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917984 | ||||||
| chr8:53917996
|
C | T | 36 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(33): Show | 36 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.511-21580C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917996 | ||||||
| chr8:53918023
|
A | G | 1 | a0001c0001t0003g0237 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.511-21553A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918023 | ||||||
| chr8:53918061
|
G | C | 1 | a0001c0003t0002g0029 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.511-21515G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918061 | ||||||
| chr8:53918118
|
T | C | 4 | a0001c0001t0002g0244a0001c0003t0001g0028a0001c0003t0003g0026others(1): Show | 4 | HG02280.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-21458T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918118 | ||||||
| chr8:53918143
|
T | C | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.511-21433T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918143 | ||||||
| chr8:53918151
|
G | A | 6 | a0001c0001t0002g0021a0001c0001t0002g0244a0001c0001t0003g0030others(3): Show | 6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-21425G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918151 | ||||||
| chr8:53918248
|
C | T | 2 | a0001c0002t0002g0004a0001c0002t0002g0007 | 2 | HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.511-21328C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918248 | ||||||
| chr8:53918249
|
C | G | 1 | a0001c0001t0002g0174 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.511-21327C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918249 | ||||||
| chr8:53918297
|
T | C | 42 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(39): Show | 42 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.511-21279T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918297 | ||||||
| chr8:53918357
|
G | A | 1 | a0001c0001t0002g0207 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.511-21219G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918357 | ||||||
| chr8:53918358
|
T | A | 3 | a0001c0001t0001g0096a0001c0001t0002g0174a0001c0001t0002g0209 | 3 | NA18943.hp2 NA18961.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.511-21218T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918358 | ||||||
| chr8:53918375
|
A | G | 27 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0049others(24): Show | 27 | HG00423.hp1 HG00609.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.511-21201A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918375 | ||||||
| chr8:53918380
|
C | CT | 36 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(33): Show | 36 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.511-21187dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53918380 | |||||
| chr8:53918386
|
T | TC | 17 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(14): Show | 17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-21190_511-2118 others(5): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918386 | ||||||
| chr8:53918390
|
C | CTTCCTT | 15 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(12): Show | 15 | HG01167.hp1 HG02055.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.511-21184_511-2118 others(10): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53918390 | |||||
| chr8:53918394
|
C | T | 17 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(14): Show | 17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-21182C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918394 | ||||||
| chr8:53918397
|
C | T | 17 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(14): Show | 17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-21179C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918397 | ||||||
| chr8:53918398
|
C | CTTTTTTT | 36 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(33): Show | 36 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.511-21177_511-2117 others(11): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53918398 | |||||
| chr8:53918398
|
C | T | 17 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(14): Show | 17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-21178C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918398 | ||||||
| chr8:53918432
|
G | A | 36 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(33): Show | 36 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.511-21144G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918432 | ||||||
| chr8:53918481
|
C | T | 1 | a0001c0001t0002g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.511-21095C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918481 | ||||||
| chr8:53918482
|
GGGTTCAA | G | 5 | a0001c0001t0001g0010a0001c0001t0002g0246a0001c0001t0004g0011others(2): Show | 5 | HG02486.hp1 HG02970.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.511-21092_511-2108 others(11): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53918482 | |||||
| chr8:53918615
|
T | C | 1 | a0001c0001t0002g0199 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.511-20961T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918615 | ||||||
| chr8:53918678
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0003g0024 | 2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.511-20898G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918678 | ||||||
| chr8:53918774
|
G | A | 1 | a0001c0001t0002g0236 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.511-20802G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918774 | ||||||
| chr8:53918789
|
A | G | 52 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0023others(49): Show | 52 | HG00741.hp1 HG01069.hp2 HG01167.hp1 others(49): Show |
intron_variant | MODIFIER | c.511-20787A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918789 | ||||||
| chr8:53919170
|
T | G | 17 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(14): Show | 17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-20406T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53919170 | ||||||
| chr8:53919288
|
C | T | 1 | a0001c0001t0001g0256 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.511-20288C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53919288 | ||||||
| chr8:53919315
|
A | G | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.511-20261A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53919315 | ||||||
| chr8:53919346
|
C | CT | 34 | a0001c0001t0001g0023a0001c0001t0001g0035a0001c0001t0001g0052others(31): Show | 34 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(31): Show |
intron_variant | MODIFIER | c.511-20215dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53919346 | |||||
| chr8:53919346
|
C | CTT | 17 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(14): Show | 17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-20216_511-2021 others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53919346 | |||||
| chr8:53919496
|
T | C | 133 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0023others(130): Show | 133 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.511-20080T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53919496 | ||||||
| chr8:53919557
|
G | C | 1 | a0001c0001t0002g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.511-20019G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53919557 | ||||||
| chr8:53919586
|
T | G | 17 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(14): Show | 17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-19990T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53919586 | ||||||
| chr8:53919596
|
T | C | 35 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(32): Show | 35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-19980T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53919596 | ||||||
| chr8:53919639
|
A | G | 17 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(14): Show | 17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-19937A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53919639 | ||||||
| chr8:53919772
|
T | C | 35 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(32): Show | 35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-19804T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53919772 | ||||||
| chr8:53919818
|
G | A | 35 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(32): Show | 35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-19758G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53919818 | ||||||
| chr8:53920030
|
T | A | 1 | a0001c0001t0001g0080 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.511-19546T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53920030 | ||||||
| chr8:53920075
|
C | T | 1 | a0001c0001t0002g0172 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.511-19501C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53920075 | ||||||
| chr8:53920131
|
T | C | 2 | a0001c0001t0005g0118a0001c0001t0005g0119 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.511-19445T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53920131 | ||||||
| chr8:53920243
|
T | C | 4 | a0001c0001t0002g0032a0001c0001t0002g0038a0001c0001t0004g0037others(1): Show | 4 | HG01167.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-19333T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53920243 | ||||||
| chr8:53920320
|
C | T | 1 | a0001c0001t0002g0073 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.511-19256C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53920320 | ||||||
| chr8:53920322
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.511-19254C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53920322 | ||||||
| chr8:53920446
|
T | A | 1 | a0001c0001t0002g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.511-19130T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53920446 | ||||||
| chr8:53920488
|
A | G | 35 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(32): Show | 35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-19088A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53920488 | ||||||
| chr8:53920589
|
T | C | 1 | a0001c0001t0002g0168 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.511-18987T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53920589 | ||||||
| chr8:53920779
|
C | T | 3 | a0001c0001t0003g0022a0001c0001t0005g0118a0001c0001t0005g0119 | 3 | HG02055.hp1 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.511-18797C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53920779 | ||||||
| chr8:53921009
|
C | T | 2 | a0001c0001t0005g0118a0001c0001t0005g0119 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.511-18567C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53921009 | ||||||
| chr8:53921011
|
C | T | 74 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0001g0068others(71): Show | 74 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.511-18565C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53921011 | ||||||
| chr8:53921070
|
G | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0107 | 2 | NA18982.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.511-18506G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53921070 | ||||||
| chr8:53921333
|
C | A | 1 | a0001c0001t0003g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.511-18243C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53921333 | ||||||
| chr8:53921405
|
G | A | 4 | a0001c0001t0002g0246a0001c0001t0004g0011a0001c0001t0004g0012others(1): Show | 4 | HG02486.hp1 HG03540.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-18171G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53921405 | ||||||
| chr8:53921442
|
CT | C | 8 | a0001c0001t0001g0031a0001c0001t0001g0112a0001c0001t0001g0147others(5): Show | 8 | HG00323.hp1 HG00323.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.511-18117delT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53921442 | |||||
| chr8:53921477
|
C | A | 35 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(32): Show | 35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-18099C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53921477 | ||||||
| chr8:53921487
|
C | A | 1 | a0001c0001t0002g0124 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.511-18089C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53921487 | ||||||
| chr8:53921632
|
G | A | 1 | a0001c0003t0002g0029 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.511-17944G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53921632 | ||||||
| chr8:53921757
|
G | A | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.511-17819G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53921757 | ||||||
| chr8:53921817
|
T | A | 131 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0023others(128): Show | 131 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.511-17759T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53921817 | ||||||
| chr8:53921877
|
T | C | 4 | a0001c0001t0002g0032a0001c0001t0002g0038a0001c0001t0004g0037others(1): Show | 4 | HG01167.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-17699T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53921877 | ||||||
| chr8:53921885
|
A | AT | 74 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0001g0068others(71): Show | 74 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.511-17687dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53921885 | |||||
| chr8:53921912
|
G | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0186 | 2 | HG00621.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.511-17664G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53921912 | ||||||
| chr8:53922087
|
T | A | 1 | a0001c0001t0001g0061 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.511-17489T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53922087 | ||||||
| chr8:53922132
|
C | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.511-17444C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53922132 | ||||||
| chr8:53922302
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.511-17274T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53922302 | ||||||
| chr8:53922325
|
G | T | 35 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(32): Show | 35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-17251G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53922325 | ||||||
| chr8:53922349
|
A | G | 35 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(32): Show | 35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-17227A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53922349 | ||||||
| chr8:53922372
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.511-17204C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53922372 | ||||||
| chr8:53922416
|
A | T | 35 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(32): Show | 35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-17160A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53922416 | ||||||
| chr8:53922427
|
A | G | 1 | a0001c0001t0002g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.511-17149A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53922427 | ||||||
| chr8:53922926
|
G | T | 10 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(7): Show | 10 | HG01496.hp2 HG02165.hp2 NA18948.hp2 others(7): Show |
intron_variant | MODIFIER | c.511-16650G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53922926 | ||||||
| chr8:53922980
|
G | A | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.511-16596G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53922980 | ||||||
| chr8:53923076
|
G | A | 35 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(32): Show | 35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-16500G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53923076 | ||||||
| chr8:53923137
|
T | C | 5 | a0001c0001t0002g0131a0001c0001t0002g0139a0001c0001t0002g0185others(2): Show | 5 | HG01243.hp1 HG01975.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.511-16439T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53923137 | ||||||
| chr8:53923200
|
G | T | 2 | a0001c0001t0006g0043a0001c0001t0006g0044 | 2 | HG01069.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.511-16376G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53923200 | ||||||
| chr8:53923212
|
G | A | 37 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(34): Show | 37 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.511-16364G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53923212 | ||||||
| chr8:53923381
|
A | T | 17 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(14): Show | 17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-16195A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53923381 | ||||||
| chr8:53923594
|
C | CA | 7 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0082others(4): Show | 7 | HG02027.hp1 NA18963.hp2 NA19055.hp1 others(4): Show |
intron_variant | MODIFIER | c.511-15969dupA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53923594 | |||||
| chr8:53923687
|
C | A | 1 | a0001c0001t0001g0097 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.511-15889C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53923687 | ||||||
| chr8:53923700
|
A | G | 1 | a0001c0003t0002g0029 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.511-15876A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53923700 | ||||||
| chr8:53923708
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.511-15868A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53923708 | ||||||
| chr8:53923726
|
C | T | 1 | a0001c0001t0002g0167 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.511-15850C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53923726 | ||||||
| chr8:53924020
|
C | A | 1 | a0001c0001t0002g0168 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.511-15556C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53924020 | ||||||
| chr8:53924345
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.511-15231G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53924345 | ||||||
| chr8:53924363
|
T | C | 74 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0001g0068others(71): Show | 74 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.511-15213T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53924363 | ||||||
| chr8:53924486
|
A | C | 35 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(32): Show | 35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-15090A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53924486 | ||||||
| chr8:53924642
|
A | G | 2 | a0001c0001t0005g0118a0001c0001t0005g0119 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.511-14934A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53924642 | ||||||
| chr8:53925436
|
A | G | 35 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(32): Show | 35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-14140A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53925436 | ||||||
| chr8:53925756
|
C | T | 2 | a0001c0001t0007g0033a0001c0001t0007g0045 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.511-13820C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53925756 | ||||||
| chr8:53925779
|
T | C | 35 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(32): Show | 35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-13797T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53925779 | ||||||
| chr8:53926034
|
C | T | 1 | a0001c0001t0002g0073 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.511-13542C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53926034 | ||||||
| chr8:53926135
|
A | G | 4 | a0001c0001t0002g0032a0001c0001t0002g0038a0001c0001t0004g0037others(1): Show | 4 | HG01167.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-13441A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53926135 | ||||||
| chr8:53926389
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0098 | 2 | NA18975.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.511-13187G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53926389 | ||||||
| chr8:53926424
|
A | G | 77 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0001g0068others(74): Show | 77 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.511-13152A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53926424 | ||||||
| chr8:53926471
|
AT | A | 15 | a0001c0001t0002g0020a0001c0001t0002g0108a0001c0001t0002g0117others(12): Show | 15 | HG01192.hp2 HG02280.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.511-13097delT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53926471 | |||||
| chr8:53926530
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.511-13046C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53926530 | ||||||
| chr8:53926686
|
C | A | 1 | a0001c0001t0002g0108 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.511-12890C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53926686 | ||||||
| chr8:53926823
|
G | C | 83 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0001g0068others(80): Show | 83 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.511-12753G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53926823 | ||||||
| chr8:53926828
|
G | A | 4 | a0001c0001t0002g0032a0001c0001t0002g0038a0001c0001t0004g0037others(1): Show | 4 | HG01167.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-12748G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53926828 | ||||||
| chr8:53926868
|
A | G | 135 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0023others(132): Show | 135 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.511-12708A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53926868 | ||||||
| chr8:53926908
|
A | G | 4 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0002g0106others(1): Show | 4 | HG01243.hp2 HG02109.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-12668A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53926908 | ||||||
| chr8:53926916
|
A | AAAAG | 35 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(32): Show | 35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-12645_511-1264 others(8): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53926916 | |||||
| chr8:53927201
|
G | GT | 31 | a0001c0001t0001g0010a0001c0001t0001g0035a0001c0001t0001g0040others(28): Show | 31 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.511-12358dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53927201 | |||||
| chr8:53927201
|
GT | G | 40 | a0001c0001t0001g0014a0001c0001t0001g0042a0001c0001t0001g0046others(37): Show | 40 | HG00423.hp1 HG00609.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.511-12358delT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53927201 | |||||
| chr8:53927201
|
GTTTT | G | 33 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(30): Show | 33 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(30): Show |
intron_variant | MODIFIER | c.511-12361_511-1235 others(8): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53927201 | |||||
| chr8:53927530
|
C | T | 2 | a0001c0001t0007g0033a0001c0001t0007g0045 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.511-12046C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53927530 | ||||||
| chr8:53928021
|
T | A | 1 | a0001c0001t0001g0074 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.511-11555T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53928021 | ||||||
| chr8:53928246
|
T | A | 16 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(13): Show | 16 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.511-11330T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53928246 | ||||||
| chr8:53928613
|
C | T | 4 | a0001c0001t0001g0112a0001c0001t0001g0116a0001c0001t0001g0197others(1): Show | 4 | HG00323.hp2 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-10963C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53928613 | ||||||
| chr8:53928723
|
T | C | 119 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(116): Show | 119 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.511-10853T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53928723 | ||||||
| chr8:53928916
|
C | T | 6 | a0001c0001t0002g0021a0001c0001t0002g0244a0001c0001t0003g0030others(3): Show | 6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-10660C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53928916 | ||||||
| chr8:53928979
|
G | C | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.511-10597G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53928979 | ||||||
| chr8:53929065
|
T | A | 77 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0001g0068others(74): Show | 77 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.511-10511T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53929065 | ||||||
| chr8:53929382
|
A | T | 1 | a0001c0001t0001g0156 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.511-10194A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53929382 | ||||||
| chr8:53929407
|
G | A | 6 | a0001c0001t0001g0018a0001c0001t0001g0050a0001c0001t0001g0130others(3): Show | 6 | HG02132.hp1 HG02886.hp1 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.511-10169G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53929407 | ||||||
| chr8:53929471
|
A | G | 83 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0001g0068others(80): Show | 83 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.511-10105A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53929471 | ||||||
| chr8:53929537
|
G | A | 83 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0001g0068others(80): Show | 83 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.511-10039G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53929537 | ||||||
| chr8:53929539
|
A | G | 35 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(32): Show | 35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-10037A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53929539 | ||||||
| chr8:53929607
|
G | T | 11 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(8): Show | 11 | HG01167.hp1 HG02055.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.511-9969G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53929607 | ||||||
| chr8:53929623
|
G | A | 5 | a0001c0001t0002g0019a0001c0001t0002g0083a0001c0001t0002g0190others(2): Show | 5 | NA18946.hp1 NA18952.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.511-9953G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53929623 | ||||||
| chr8:53929726
|
T | C | 6 | a0001c0001t0001g0088a0001c0001t0001g0092a0001c0001t0001g0098others(3): Show | 6 | HG00642.hp2 HG01358.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-9850T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53929726 | ||||||
| chr8:53930019
|
A | G | 35 | a0001c0001t0001g0031a0001c0001t0001g0035a0001c0001t0001g0036others(32): Show | 35 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.511-9557A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53930019 | ||||||
| chr8:53930069
|
T | A | 1 | a0001c0001t0002g0175 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.511-9507T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53930069 | ||||||
| chr8:53930070
|
T | A | 1 | a0001c0001t0002g0175 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.511-9506T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53930070 | ||||||
| chr8:53930587
|
C | T | 16 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(13): Show | 16 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.511-8989C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53930587 | ||||||
| chr8:53930602
|
G | A | 1 | a0001c0001t0002g0165 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.511-8974G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53930602 | ||||||
| chr8:53930773
|
T | C | 35 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(32): Show | 35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-8803T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53930773 | ||||||
| chr8:53930795
|
T | A | 1 | a0001c0001t0001g0147 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.511-8781T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53930795 | ||||||
| chr8:53931053
|
C | G | 119 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(116): Show | 119 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.511-8523C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53931053 | ||||||
| chr8:53931260
|
T | C | 2 | a0001c0001t0002g0243a0001c0001t0002g0245 | 2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.511-8316T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53931260 | ||||||
| chr8:53931321
|
C | T | 6 | a0001c0001t0002g0021a0001c0001t0002g0244a0001c0001t0003g0030others(3): Show | 6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-8255C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53931321 | ||||||
| chr8:53931355
|
G | A | 119 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(116): Show | 119 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.511-8221G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53931355 | ||||||
| chr8:53931423
|
T | G | 1 | a0001c0001t0001g0048 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.511-8153T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53931423 | ||||||
| chr8:53931552
|
A | AAAC | 24 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0001g0047others(21): Show | 24 | HG00323.hp2 HG00597.hp1 HG01993.hp1 others(21): Show |
intron_variant | MODIFIER | c.511-7985_511-7983d others(5): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53931552 | |||||
| chr8:53931552
|
A | AAACAAC | 13 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(10): Show | 13 | HG00438.hp2 HG00609.hp1 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.511-7988_511-7983d others(8): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53931552 | |||||
| chr8:53931552
|
A | AAACAACA others(2): Show |
3 | a0001c0001t0001g0116a0001c0001t0001g0197a0001c0001t0001g0202 | 3 | HG01167.hp2 HG01169.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.511-7991_511-7983d others(11): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53931552 | |||||
| chr8:53931552
|
AAACAAC | A | 24 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0049others(21): Show | 24 | HG00423.hp1 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.511-7988_511-7983d others(8): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53931552 | |||||
| chr8:53931552
|
AAACAACA others(2): Show |
A | 3 | a0001c0001t0005g0118a0001c0001t0005g0119a0001c0003t0002g0025 | 3 | HG02055.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.511-7991_511-7983d others(11): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53931552 | |||||
| chr8:53931552
|
AAACAACA others(5): Show |
A | 55 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0023others(52): Show | 55 | HG00741.hp1 HG01069.hp2 HG01167.hp1 others(52): Show |
intron_variant | MODIFIER | c.511-7994_511-7983d others(14): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53931552 | |||||
| chr8:53931552
|
AAACAACA others(8): Show |
A | 77 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0001g0068others(74): Show | 77 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.511-7997_511-7983d others(17): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53931552 | |||||
| chr8:53931571
|
A | G | 1 | a0001c0001t0002g0214 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.511-8005A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53931571 | ||||||
| chr8:53931731
|
T | C | 14 | a0001c0001t0001g0054a0001c0001t0001g0064a0001c0001t0001g0074others(11): Show | 14 | HG01496.hp2 HG02027.hp2 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.511-7845T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53931731 | ||||||
| chr8:53931733
|
G | A | 4 | a0001c0001t0002g0244a0001c0003t0001g0028a0001c0003t0003g0026others(1): Show | 4 | HG02280.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-7843G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53931733 | ||||||
| chr8:53931973
|
C | T | 76 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0001g0068others(73): Show | 76 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.511-7603C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53931973 | ||||||
| chr8:53932139
|
G | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(9): Show | 12 | HG01167.hp1 HG02055.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.511-7437G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53932139 | ||||||
| chr8:53932227
|
T | C | 1 | a0001c0001t0001g0231 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.511-7349T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53932227 | ||||||
| chr8:53932271
|
G | A | 1 | a0001c0001t0003g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.511-7305G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53932271 | ||||||
| chr8:53932365
|
A | G | 35 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(32): Show | 35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-7211A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53932365 | ||||||
| chr8:53932585
|
T | C | 119 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(116): Show | 119 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.511-6991T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53932585 | ||||||
| chr8:53932839
|
C | T | 1 | a0001c0001t0003g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.511-6737C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53932839 | ||||||
| chr8:53932974
|
G | A | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.511-6602G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53932974 | ||||||
| chr8:53933008
|
C | T | 3 | a0001c0001t0001g0093a0001c0001t0001g0105a0001c0001t0001g0163 | 3 | NA18957.hp1 NA18961.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.511-6568C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53933008 | ||||||
| chr8:53933052
|
G | A | 1 | a0001c0001t0003g0170 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.511-6524G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53933052 | ||||||
| chr8:53933057
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.511-6519A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53933057 | ||||||
| chr8:53933070
|
A | G | 2 | a0001c0001t0005g0118a0001c0001t0005g0119 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.511-6506A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53933070 | ||||||
| chr8:53933168
|
A | G | 1 | a0001c0001t0001g0152 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.511-6408A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53933168 | ||||||
| chr8:53933338
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.511-6238A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53933338 | ||||||
| chr8:53933471
|
A | G | 1 | a0001c0001t0002g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.511-6105A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53933471 | ||||||
| chr8:53933481
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.511-6095G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53933481 | ||||||
| chr8:53933653
|
G | A | 75 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0001g0068others(72): Show | 75 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.511-5923G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53933653 | ||||||
| chr8:53933708
|
T | G | 1 | a0001c0001t0003g0051 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.511-5868T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53933708 | ||||||
| chr8:53933733
|
C | T | 36 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(33): Show | 36 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.511-5843C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53933733 | ||||||
| chr8:53933765
|
G | A | 36 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(33): Show | 36 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.511-5811G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53933765 | ||||||
| chr8:53933805
|
A | G | 6 | a0001c0001t0002g0021a0001c0001t0002g0244a0001c0001t0003g0030others(3): Show | 6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-5771A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53933805 | ||||||
| chr8:53934048
|
A | G | 83 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0001g0068others(80): Show | 83 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.511-5528A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53934048 | ||||||
| chr8:53934162
|
T | C | 1 | a0001c0001t0002g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.511-5414T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53934162 | ||||||
| chr8:53934476
|
A | G | 1 | a0001c0001t0002g0073 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.511-5100A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53934476 | ||||||
| chr8:53934477
|
C | A | 35 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(32): Show | 35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-5099C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53934477 | ||||||
| chr8:53934547
|
C | G | 1 | a0001c0001t0001g0031 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.511-5029C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53934547 | ||||||
| chr8:53934574
|
T | C | 1 | a0001c0001t0001g0147 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.511-5002T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53934574 | ||||||
| chr8:53934636
|
C | T | 35 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(32): Show | 35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-4940C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53934636 | ||||||
| chr8:53934661
|
G | A | 36 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(33): Show | 36 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.511-4915G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53934661 | ||||||
| chr8:53934873
|
C | T | 1 | a0001c0001t0002g0144 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.511-4703C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53934873 | ||||||
| chr8:53935000
|
T | C | 135 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0023others(132): Show | 135 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.511-4576T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53935000 | ||||||
| chr8:53935075
|
A | T | 1 | a0001c0001t0001g0189 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.511-4501A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53935075 | ||||||
| chr8:53935099
|
A | C | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.511-4477A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53935099 | ||||||
| chr8:53935254
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.511-4322A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53935254 | ||||||
| chr8:53935359
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.511-4217C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53935359 | ||||||
| chr8:53935427
|
C | T | 1 | a0001c0001t0002g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.511-4149C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53935427 | ||||||
| chr8:53935521
|
C | T | 5 | a0001c0001t0001g0010a0001c0001t0002g0246a0001c0001t0004g0011others(2): Show | 5 | HG02486.hp1 HG02970.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.511-4055C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53935521 | ||||||
| chr8:53935547
|
T | C | 1 | a0001c0001t0002g0226 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.511-4029T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53935547 | ||||||
| chr8:53935780
|
C | G | 134 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0023others(131): Show | 134 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.511-3796C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53935780 | ||||||
| chr8:53935800
|
G | C | 1 | a0001c0001t0002g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.511-3776G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53935800 | ||||||
| chr8:53935864
|
A | G | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.511-3712A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53935864 | ||||||
| chr8:53935904
|
T | C | 6 | a0001c0001t0002g0021a0001c0001t0002g0244a0001c0001t0003g0030others(3): Show | 6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-3672T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53935904 | ||||||
| chr8:53935932
|
G | C | 1 | a0001c0001t0001g0125 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.511-3644G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53935932 | ||||||
| chr8:53936049
|
C | A | 1 | a0001c0001t0002g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.511-3527C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53936049 | ||||||
| chr8:53936466
|
G | C | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG02818.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.511-3110G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53936466 | ||||||
| chr8:53936491
|
G | C | 132 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0023others(129): Show | 132 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.511-3085G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53936491 | ||||||
| chr8:53936623
|
T | A | 82 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0001g0068others(79): Show | 82 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.511-2953T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53936623 | ||||||
| chr8:53936675
|
C | A | 20 | a0001c0001t0001g0052a0001c0001t0001g0054a0001c0001t0001g0064others(17): Show | 20 | HG01496.hp2 HG02027.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.511-2901C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53936675 | ||||||
| chr8:53936699
|
C | T | 2 | a0001c0001t0007g0033a0001c0001t0007g0045 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.511-2877C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53936699 | ||||||
| chr8:53936700
|
G | A | 1 | a0001c0001t0009g0128 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.511-2876G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53936700 | ||||||
| chr8:53936875
|
T | C | 6 | a0001c0001t0002g0021a0001c0001t0002g0244a0001c0001t0003g0030others(3): Show | 6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-2701T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53936875 | ||||||
| chr8:53937082
|
A | C | 1 | a0001c0001t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.511-2494A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53937082 | ||||||
| chr8:53937119
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.511-2457C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53937119 | ||||||
| chr8:53937128
|
C | A | 6 | a0001c0001t0002g0021a0001c0001t0002g0244a0001c0001t0003g0030others(3): Show | 6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-2448C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53937128 | ||||||
| chr8:53937406
|
A | G | 36 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(33): Show | 36 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.511-2170A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53937406 | ||||||
| chr8:53937611
|
A | T | 1 | a0001c0001t0003g0181 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.511-1965A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53937611 | ||||||
| chr8:53937617
|
T | A | 1 | a0001c0003t0004g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.511-1959T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53937617 | ||||||
| chr8:53937677
|
A | C | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG02165.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.511-1899A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53937677 | ||||||
| chr8:53937729
|
A | G | 35 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(32): Show | 35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-1847A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53937729 | ||||||
| chr8:53937773
|
A | G | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG01074.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.511-1803A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53937773 | ||||||
| chr8:53937791
|
C | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.511-1785C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53937791 | ||||||
| chr8:53937831
|
G | T | 1 | a0001c0001t0001g0112 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.511-1745G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53937831 | ||||||
| chr8:53937839
|
G | A | 2 | a0001c0001t0007g0033a0001c0001t0007g0045 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.511-1737G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53937839 | ||||||
| chr8:53938053
|
G | T | 2 | a0001c0001t0001g0092a0001c0001t0001g0098 | 2 | NA18975.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.511-1523G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53938053 | ||||||
| chr8:53938249
|
C | T | 134 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0023others(131): Show | 134 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.511-1327C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53938249 | ||||||
| chr8:53938312
|
T | G | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.511-1264T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53938312 | ||||||
| chr8:53938712
|
A | G | 34 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(31): Show | 34 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(31): Show |
intron_variant | MODIFIER | c.511-864A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53938712 | ||||||
| chr8:53938906
|
G | A | 1 | a0001c0001t0002g0150 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.511-670G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53938906 | ||||||
| chr8:53939242
|
G | C | 14 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(11): Show | 14 | HG01069.hp2 HG01167.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.511-334G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53939242 | ||||||
| chr8:53939256
|
T | A | 1 | a0001c0001t0001g0161 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.511-320T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53939256 | ||||||
| chr8:53939259
|
GTAGCACT others(3): Show |
G | 3 | a0001c0001t0001g0116a0001c0001t0001g0197a0001c0001t0001g0202 | 3 | HG01167.hp2 HG01169.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.511-315_511-306del others(10): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53939259 | |||||
| chr8:53939270
|
T | C | 3 | a0001c0001t0001g0116a0001c0001t0001g0197a0001c0001t0001g0202 | 3 | HG01167.hp2 HG01169.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.511-306T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53939270 | ||||||
| chr8:53939282
|
A | G | 2 | a0001c0001t0002g0053a0001c0001t0002g0070 | 2 | NA18943.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.511-294A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53939282 | ||||||
| chr8:53939332
|
G | C | 14 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0143others(11): Show | 14 | HG01069.hp2 HG01167.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.511-244G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53939332 | ||||||
| chr8:53939891
|
A | G | 6 | a0001c0001t0001g0010a0001c0001t0001g0143a0001c0001t0002g0246others(3): Show | 6 | HG02486.hp1 HG02622.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.659+167A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53939891 | ||||||
| chr8:53940039
|
C | T | 48 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0023others(45): Show | 48 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.659+315C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53940039 | ||||||
| chr8:53940083
|
C | G | 111 | a0001c0001t0001g0031a0001c0001t0001g0035a0001c0001t0001g0036others(108): Show | 111 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.659+359C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53940083 | ||||||
| chr8:53940098
|
G | A | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.659+374G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53940098 | ||||||
| chr8:53940227
|
T | C | 164 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0023others(161): Show | 164 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.659+503T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53940227 | ||||||
| chr8:53940542
|
G | C | 35 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(32): Show | 35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.659+818G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53940542 | ||||||
| chr8:53940546
|
A | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.659+822A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53940546 | ||||||
| chr8:53940577
|
G | A | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG01074.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.659+853G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53940577 | ||||||
| chr8:53940876
|
C | T | 2 | a0001c0001t0002g0218a0001c0001t0002g0223 | 2 | HG01070.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.659+1152C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53940876 | ||||||
| chr8:53941145
|
T | G | 165 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0023others(162): Show | 165 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.659+1421T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53941145 | ||||||
| chr8:53941994
|
C | T | 1 | a0001c0001t0002g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.659+2270C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53941994 | ||||||
| chr8:53942214
|
G | C | 1 | a0001c0001t0001g0186 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.659+2490G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53942214 | ||||||
| chr8:53942361
|
G | A | 38 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0054others(35): Show | 38 | HG00741.hp1 HG01167.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.659+2637G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53942361 | ||||||
| chr8:53942567
|
T | A | 1 | a0001c0001t0002g0235 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.659+2843T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53942567 | ||||||
| chr8:53942602
|
T | C | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.659+2878T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53942602 | ||||||
| chr8:53942617
|
G | A | 1 | a0001c0001t0002g0235 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.659+2893G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53942617 | ||||||
| chr8:53942826
|
TA | T | 194 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(191): Show | 194 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.659+3121delA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 53942826 | |||||
| chr8:53942826
|
TAA | T | 5 | a0001c0001t0001g0088a0001c0001t0003g0051a0001c0001t0005g0119others(2): Show | 5 | HG01069.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.659+3120_659+3121d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 53942826 | |||||
| chr8:53943025
|
A | G | 1 | a0001c0001t0002g0144 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.659+3301A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53943025 | ||||||
| chr8:53943120
|
T | C | 112 | a0001c0001t0001g0031a0001c0001t0001g0035a0001c0001t0001g0036others(109): Show | 112 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.659+3396T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53943120 | ||||||
| chr8:53943202
|
C | A | 1 | a0001c0001t0002g0122 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.660-3463C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53943202 | ||||||
| chr8:53943267
|
A | G | 12 | a0001c0001t0001g0054a0001c0001t0001g0075a0001c0001t0001g0076others(9): Show | 12 | HG02027.hp2 HG02165.hp2 HG04184.hp1 others(9): Show |
intron_variant | MODIFIER | c.660-3398A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53943267 | ||||||
| chr8:53943312
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.660-3353C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53943312 | ||||||
| chr8:53943615
|
C | A | 1 | a0001c0001t0002g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.660-3050C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53943615 | ||||||
| chr8:53943741
|
A | AT | 151 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0035others(148): Show | 151 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.660-2924_660-2923i others(3): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53943741 | ||||||
| chr8:53943996
|
T | TAC | 9 | a0001c0001t0001g0100a0001c0001t0001g0163a0001c0001t0001g0231others(6): Show | 9 | HG02040.hp1 HG02055.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.660-2642_660-2641d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 53943996 | |||||
| chr8:53943996
|
TAC | T | 8 | a0001c0001t0001g0023a0001c0001t0001g0069a0001c0001t0001g0092others(5): Show | 8 | HG02809.hp2 HG02886.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.660-2642_660-2641d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 53943996 | |||||
| chr8:53943996
|
TACACAC | T | 26 | a0001c0001t0001g0052a0001c0001t0001g0054a0001c0001t0001g0075others(23): Show | 26 | HG00741.hp1 HG01109.hp2 HG02027.hp2 others(23): Show |
intron_variant | MODIFIER | c.660-2646_660-2641d others(8): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 53943996 | |||||
| chr8:53944078
|
T | TAAAG | 144 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0035others(141): Show | 144 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.660-2586_660-2585i others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 53944078 | |||||
| chr8:53944136
|
A | G | 1 | a0001c0001t0001g0096 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.660-2529A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53944136 | ||||||
| chr8:53944322
|
A | G | 98 | a0001c0001t0001g0031a0001c0001t0001g0035a0001c0001t0001g0036others(95): Show | 98 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.660-2343A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53944322 | ||||||
| chr8:53944345
|
A | G | 1 | a0001c0001t0002g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.660-2320A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53944345 | ||||||
| chr8:53944410
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.660-2255C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53944410 | ||||||
| chr8:53944450
|
A | C | 1 | a0001c0001t0002g0232 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.660-2215A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53944450 | ||||||
| chr8:53944453
|
A | G | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.660-2212A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53944453 | ||||||
| chr8:53944460
|
C | T | 3 | a0001c0001t0005g0118a0001c0001t0005g0119a0001c0003t0002g0025 | 3 | HG02055.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.660-2205C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53944460 | ||||||
| chr8:53944535
|
C | T | 177 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0031others(174): Show | 177 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.660-2130C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53944535 | ||||||
| chr8:53944537
|
C | CA | 76 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0041others(73): Show | 76 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.660-2113dupA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 53944537 | |||||
| chr8:53944537
|
CA | C | 14 | a0001c0001t0001g0023a0001c0001t0002g0111a0001c0001t0002g0162others(11): Show | 14 | HG00323.hp1 HG01257.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.660-2113delA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 53944537 | |||||
| chr8:53944561
|
G | C | 1 | a0001c0001t0001g0060 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.660-2104G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53944561 | ||||||
| chr8:53944641
|
C | T | 1 | a0001c0001t0002g0235 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.660-2024C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53944641 | ||||||
| chr8:53944672
|
T | C | 2 | a0001c0001t0002g0021a0001c0001t0011g0208 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.660-1993T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53944672 | ||||||
| chr8:53944748
|
G | A | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.660-1917G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53944748 | ||||||
| chr8:53944807
|
C | G | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.660-1858C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53944807 | ||||||
| chr8:53945028
|
C | T | 7 | a0001c0001t0002g0021a0001c0001t0002g0144a0001c0001t0005g0118others(4): Show | 7 | HG02055.hp1 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.660-1637C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53945028 | ||||||
| chr8:53945140
|
G | A | 71 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(68): Show | 71 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.660-1525G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53945140 | ||||||
| chr8:53945381
|
C | G | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.660-1284C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53945381 | ||||||
| chr8:53945482
|
T | C | 1 | a0001c0001t0002g0167 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.660-1183T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53945482 | ||||||
| chr8:53945809
|
A | T | 1 | a0001c0001t0001g0255 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.660-856A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53945809 | ||||||
| chr8:53945844
|
G | A | 3 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0008g0039 | 3 | HG01069.hp2 HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.660-821G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53945844 | ||||||
| chr8:53945887
|
C | CA | 43 | a0001c0001t0001g0081a0001c0001t0001g0090a0001c0001t0001g0093others(40): Show | 43 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.660-765dupA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 53945887 | |||||
| chr8:53945934
|
G | A | 140 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(137): Show | 140 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.660-731G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53945934 | ||||||
| chr8:53946107
|
A | G | 2 | a0001c0001t0002g0117a0001c0001t0002g0210 | 2 | HG02280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.660-558A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53946107 | ||||||
| chr8:53946162
|
T | A | 2 | a0001c0001t0002g0021a0001c0001t0011g0208 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.660-503T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53946162 | ||||||
| chr8:53946229
|
T | A | 1 | a0001c0001t0001g0010 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.660-436T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53946229 | ||||||
| chr8:53946421
|
T | A | 47 | a0001c0001t0001g0031a0001c0001t0001g0035a0001c0001t0001g0036others(44): Show | 47 | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.660-244T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53946421 | ||||||
| chr8:53946469
|
T | C | 143 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(140): Show | 143 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.660-196T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53946469 | ||||||
| chr8:53946947
|
A | G | 1 | a0001c0002t0001g0005 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.743+199A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53946947 | ||||||
| chr8:53947034
|
T | C | 1 | a0001c0001t0001g0062 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.743+286T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947034 | ||||||
| chr8:53947058
|
A | G | 3 | a0001c0001t0005g0118a0001c0001t0005g0119a0001c0003t0002g0025 | 3 | HG02055.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.743+310A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947058 | ||||||
| chr8:53947135
|
T | A | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+387T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947135 | ||||||
| chr8:53947167
|
C | T | 1 | a0001c0001t0002g0236 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.743+419C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947167 | ||||||
| chr8:53947168
|
T | G | 217 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(214): Show | 217 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.743+420T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947168 | ||||||
| chr8:53947193
|
A | T | 8 | a0001c0001t0001g0115a0001c0001t0002g0053a0001c0001t0002g0070others(5): Show | 8 | HG01099.hp1 HG01496.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.743+445A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947193 | ||||||
| chr8:53947194
|
C | T | 8 | a0001c0001t0001g0115a0001c0001t0002g0053a0001c0001t0002g0070others(5): Show | 8 | HG01099.hp1 HG01496.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.743+446C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947194 | ||||||
| chr8:53947196
|
C | CGCTATAT others(51): Show |
2 | a0001c0001t0005g0118a0001c0001t0005g0119 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.743+473_743+474ins others(58): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947196 | |||||
| chr8:53947196
|
C | CGCTATAT others(88): Show |
1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+473_743+474ins others(95): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947196 | |||||
| chr8:53947196
|
C | T | 1 | a0001c0001t0003g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.743+448C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947196 | ||||||
| chr8:53947196
|
CGCTATAT others(26): Show |
C | 1 | a0001c0001t0001g0254 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.743+503_743+535del others(33): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947196 | |||||
| chr8:53947207
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.743+459A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947207 | ||||||
| chr8:53947216
|
A | G | 15 | a0001c0001t0002g0020a0001c0001t0002g0038a0001c0001t0002g0108others(12): Show | 15 | HG01192.hp2 HG01891.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.743+468A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947216 | ||||||
| chr8:53947247
|
ATATT | A | 3 | a0001c0001t0005g0118a0001c0001t0005g0119a0001c0001t0011g0208 | 3 | HG02055.hp1 HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.743+507_743+510del others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947247 | |||||
| chr8:53947251
|
T | A | 8 | a0001c0001t0001g0115a0001c0001t0002g0053a0001c0001t0002g0070others(5): Show | 8 | HG01099.hp1 HG01496.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.743+503T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947251 | ||||||
| chr8:53947284
|
A | T | 5 | a0001c0001t0002g0235a0001c0001t0006g0043a0001c0001t0006g0044others(2): Show | 5 | HG01069.hp2 HG01109.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.743+536A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947284 | ||||||
| chr8:53947300
|
T | C | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+552T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947300 | ||||||
| chr8:53947307
|
TATAGTAT others(25): Show |
T | 2 | a0001c0001t0001g0069a0001c0001t0002g0207 | 2 | HG00438.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.743+595_743+626del others(32): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947307 | |||||
| chr8:53947308
|
A | G | 2 | a0001c0001t0005g0118a0001c0001t0005g0119 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.743+560A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947308 | ||||||
| chr8:53947312
|
T | C | 16 | a0001c0001t0001g0023a0001c0001t0002g0235a0001c0001t0003g0001others(13): Show | 16 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.743+564T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947312 | ||||||
| chr8:53947319
|
A | AT | 3 | a0001c0001t0002g0235a0001c0003t0002g0025a0001c0003t0002g0029 | 3 | HG01109.hp2 HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.743+573dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947319 | |||||
| chr8:53947325
|
T | C | 5 | a0001c0001t0002g0235a0001c0001t0005g0118a0001c0001t0005g0119others(2): Show | 5 | HG01109.hp2 HG02055.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.743+577T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947325 | ||||||
| chr8:53947336
|
T | A | 5 | a0001c0001t0002g0235a0001c0001t0005g0118a0001c0001t0005g0119others(2): Show | 5 | HG01109.hp2 HG02055.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.743+588T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947336 | ||||||
| chr8:53947337
|
A | G | 5 | a0001c0001t0002g0235a0001c0001t0005g0118a0001c0001t0005g0119others(2): Show | 5 | HG01109.hp2 HG02055.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.743+589A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947337 | ||||||
| chr8:53947339
|
G | T | 5 | a0001c0001t0002g0235a0001c0001t0005g0118a0001c0001t0005g0119others(2): Show | 5 | HG01109.hp2 HG02055.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.743+591G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947339 | ||||||
| chr8:53947343
|
G | T | 1 | a0001c0001t0001g0049 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.743+595G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947343 | ||||||
| chr8:53947344
|
T | A | 1 | a0001c0001t0001g0049 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.743+596T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947344 | ||||||
| chr8:53947344
|
T | C | 1 | a0001c0003t0002g0029 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.743+596T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947344 | ||||||
| chr8:53947345
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.743+597A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947345 | ||||||
| chr8:53947351
|
ATT | A | 4 | a0001c0001t0003g0030a0001c0001t0003g0102a0001c0001t0003g0103others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.743+604_743+605del others(2): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947351 | ||||||
| chr8:53947361
|
CTA | C | 4 | a0001c0001t0002g0235a0001c0001t0005g0118a0001c0001t0005g0119others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.743+620_743+621del others(2): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947361 | |||||
| chr8:53947375
|
T | G | 5 | a0001c0001t0002g0235a0001c0001t0005g0118a0001c0001t0005g0119others(2): Show | 5 | HG01109.hp2 HG02055.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.743+627T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947375 | ||||||
| chr8:53947376
|
A | T | 5 | a0001c0001t0002g0235a0001c0001t0005g0118a0001c0001t0005g0119others(2): Show | 5 | HG01109.hp2 HG02055.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.743+628A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947376 | ||||||
| chr8:53947377
|
G | A | 5 | a0001c0001t0002g0235a0001c0001t0005g0118a0001c0001t0005g0119others(2): Show | 5 | HG01109.hp2 HG02055.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.743+629G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947377 | ||||||
| chr8:53947380
|
T | C | 37 | a0001c0001t0001g0093a0001c0001t0001g0105a0001c0001t0001g0120others(34): Show | 37 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.743+632T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947380 | ||||||
| chr8:53947382
|
T | TA | 5 | a0001c0001t0002g0235a0001c0001t0005g0118a0001c0001t0005g0119others(2): Show | 5 | HG01109.hp2 HG02055.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.743+634_743+635ins others(1): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947382 | ||||||
| chr8:53947383
|
TTA | T | 37 | a0001c0001t0001g0093a0001c0001t0001g0105a0001c0001t0001g0120others(34): Show | 37 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.743+641_743+642del others(2): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947383 | |||||
| chr8:53947408
|
G | GTATA | 141 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(138): Show | 141 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.743+662_743+663ins others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947408 | |||||
| chr8:53947411
|
C | T | 5 | a0001c0001t0002g0235a0001c0001t0005g0118a0001c0001t0005g0119others(2): Show | 5 | HG01109.hp2 HG02055.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.743+663C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947411 | ||||||
| chr8:53947430
|
T | TAA | 5 | a0001c0001t0002g0235a0001c0001t0005g0118a0001c0001t0005g0119others(2): Show | 5 | HG01109.hp2 HG02055.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.743+682_743+683ins others(2): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947430 | ||||||
| chr8:53947440
|
T | C | 4 | a0001c0001t0002g0106a0001c0001t0002g0232a0001c0001t0007g0033others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.743+692T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947440 | ||||||
| chr8:53947463
|
TAA | T | 3 | a0001c0001t0002g0235a0001c0003t0002g0025a0001c0003t0002g0029 | 3 | HG01109.hp2 HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.743+716_743+717del others(2): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947463 | ||||||
| chr8:53947465
|
AGATATAG others(26): Show |
A | 1 | a0001c0001t0001g0063 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.743+816_743+848del others(33): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947465 | |||||
| chr8:53947491
|
C | CTA | 3 | a0001c0001t0002g0235a0001c0003t0002g0025a0001c0003t0002g0029 | 3 | HG01109.hp2 HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.743+748_743+749dup others(2): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947491 | |||||
| chr8:53947498
|
G | A | 3 | a0001c0001t0002g0235a0001c0003t0002g0025a0001c0003t0002g0029 | 3 | HG01109.hp2 HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.743+750G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947498 | ||||||
| chr8:53947498
|
G | T | 2 | a0001c0001t0005g0118a0001c0001t0005g0119 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.743+750G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947498 | ||||||
| chr8:53947519
|
A | G | 2 | a0001c0001t0005g0118a0001c0001t0005g0119 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.743+771A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947519 | ||||||
| chr8:53947531
|
G | A | 2 | a0001c0001t0005g0118a0001c0001t0005g0119 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.743+783G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947531 | ||||||
| chr8:53947541
|
TATACATT others(61): Show |
T | 4 | a0001c0001t0003g0022a0001c0001t0006g0043a0001c0001t0006g0044others(1): Show | 4 | HG01069.hp2 HG02630.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.743+816_743+883del others(68): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947541 | |||||
| chr8:53947557
|
C | CTA | 53 | a0001c0001t0001g0018a0001c0001t0001g0041a0001c0001t0001g0042others(50): Show | 53 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.743+814_743+815dup others(2): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947557 | |||||
| chr8:53947557
|
CTATATAG others(28): Show |
C | 7 | a0001c0001t0001g0189a0001c0001t0004g0011a0001c0001t0004g0012others(4): Show | 7 | HG00609.hp1 HG01167.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.743+826_743+860del others(35): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947557 | |||||
| chr8:53947574
|
T | C | 13 | a0001c0001t0001g0054a0001c0001t0001g0071a0001c0001t0001g0077others(10): Show | 13 | HG00140.hp2 HG00741.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.743+826T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947574 | ||||||
| chr8:53947574
|
T | TATACATT others(28): Show |
1 | a0001c0001t0002g0214 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.743+1001_743+1035d others(37): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947574 | |||||
| chr8:53947574
|
TATACATT others(28): Show |
T | 17 | a0001c0001t0001g0023a0001c0001t0002g0021a0001c0001t0003g0001others(14): Show | 17 | HG01891.hp2 HG02109.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.743+1001_743+1035d others(37): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947574 | |||||
| chr8:53947579
|
A | T | 1 | a0001c0001t0001g0071 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.743+831A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947579 | ||||||
| chr8:53947590
|
CTA | C | 38 | a0001c0001t0001g0014a0001c0001t0001g0120a0001c0001t0001g0163others(35): Show | 38 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.743+849_743+850del others(2): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947590 | |||||
| chr8:53947592
|
A | ATATAGGA others(24): Show |
1 | a0001c0001t0002g0182 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.743+848_743+849ins others(31): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947592 | |||||
| chr8:53947609
|
C | T | 5 | a0001c0001t0001g0014a0001c0001t0005g0118a0001c0001t0005g0119others(2): Show | 5 | HG02055.hp1 HG02886.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.743+861C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947609 | ||||||
| chr8:53947679
|
CATACATT others(133): Show |
C | 2 | a0001c0001t0003g0102a0001c0001t0003g0103 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.743+966_743+1105de others(1): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947679 | |||||
| chr8:53947695
|
C | T | 21 | a0001c0001t0002g0016a0001c0001t0002g0038a0001c0001t0002g0108others(18): Show | 21 | HG01192.hp2 HG01891.hp1 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.743+947C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947695 | ||||||
| chr8:53947714
|
C | T | 130 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(127): Show | 130 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.743+966C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947714 | ||||||
| chr8:53947730
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.743+982C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947730 | ||||||
| chr8:53947749
|
C | T | 145 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(142): Show | 145 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.743+1001C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947749 | ||||||
| chr8:53947749
|
CATACATT others(28): Show |
C | 2 | a0001c0001t0002g0122a0001c0001t0002g0150 | 2 | HG00140.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.743+1096_743+1130d others(37): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947749 | |||||
| chr8:53947784
|
T | C | 36 | a0001c0001t0001g0093a0001c0001t0001g0105a0001c0001t0001g0120others(33): Show | 36 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.743+1036T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947784 | ||||||
| chr8:53947809
|
G | A | 7 | a0001c0001t0001g0054a0001c0001t0001g0077a0001c0001t0001g0085others(4): Show | 7 | HG02027.hp2 HG02083.hp1 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.743+1061G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947809 | ||||||
| chr8:53947813
|
A | ATAGTATA others(28): Show |
1 | a0001c0001t0001g0252 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.743+1095_743+1096i others(37): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947813 | |||||
| chr8:53947813
|
A | G | 8 | a0001c0001t0001g0054a0001c0001t0001g0077a0001c0001t0001g0085others(5): Show | 8 | HG02027.hp2 HG02083.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.743+1065A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947813 | ||||||
| chr8:53947823
|
C | T | 3 | a0001c0001t0005g0118a0001c0001t0005g0119a0001c0003t0002g0025 | 3 | HG02055.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.743+1075C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947823 | ||||||
| chr8:53947844
|
G | A | 134 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(131): Show | 134 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.743+1096G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947844 | ||||||
| chr8:53947848
|
A | ATAGTATA others(28): Show |
6 | a0001c0001t0001g0064a0001c0001t0001g0086a0001c0001t0001g0096others(3): Show | 6 | HG02451.hp1 HG02572.hp1 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.743+1110_743+1144d others(37): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947848 | |||||
| chr8:53947848
|
A | G | 134 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(131): Show | 134 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.743+1100A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947848 | ||||||
| chr8:53947858
|
C | T | 3 | a0001c0001t0005g0118a0001c0001t0005g0119a0001c0003t0002g0025 | 3 | HG02055.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.743+1110C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947858 | ||||||
| chr8:53947874
|
A | G | 1 | a0001c0001t0002g0235 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.743+1126A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947874 | ||||||
| chr8:53947890
|
A | C | 1 | a0001c0001t0002g0235 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.743+1142A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947890 | ||||||
| chr8:53947911
|
T | C | 2 | a0001c0001t0002g0034a0001c0001t0002g0073 | 2 | HG03669.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.743+1163T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947911 | ||||||
| chr8:53947913
|
G | T | 2 | a0001c0001t0005g0118a0001c0001t0005g0119 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.743+1165G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947913 | ||||||
| chr8:53948070
|
T | TTATATAT others(20): Show |
3 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0008g0039 | 3 | HG01069.hp2 HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.743+1367_743+1393d others(29): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948070 | |||||
| chr8:53948124
|
A | ATATATAT others(28): Show |
2 | a0001c0001t0003g0022a0001c0001t0003g0051 | 2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.743+1414_743+1448d others(37): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948124 | |||||
| chr8:53948124
|
ATATATAT others(28): Show |
A | 1 | a0001c0001t0002g0235 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.743+1414_743+1448d others(37): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948124 | |||||
| chr8:53948133
|
CTA | C | 3 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013 | 3 | HG03540.hp1 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.743+1393_743+1394d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948133 | |||||
| chr8:53948135
|
A | ATATATAT others(28): Show |
2 | a0001c0001t0005g0118a0001c0001t0005g0119 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.743+1421_743+1422i others(37): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948135 | |||||
| chr8:53948210
|
TAA | T | 47 | a0001c0001t0001g0031a0001c0001t0001g0035a0001c0001t0001g0036others(44): Show | 47 | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.743+1463_743+1464d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948210 | ||||||
| chr8:53948211
|
A | G | 2 | a0001c0001t0005g0118a0001c0001t0005g0119 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.743+1463A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948211 | ||||||
| chr8:53948213
|
G | T | 2 | a0001c0001t0005g0118a0001c0001t0005g0119 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.743+1465G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948213 | ||||||
| chr8:53948250
|
GTATA | G | 3 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0008g0039 | 3 | HG01069.hp2 HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.743+1507_743+1510d others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948250 | |||||
| chr8:53948295
|
G | A | 1 | a0001c0001t0002g0235 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.743+1547G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948295 | ||||||
| chr8:53948318
|
ATATG | A | 3 | a0001c0001t0005g0118a0001c0001t0005g0119a0001c0003t0002g0025 | 3 | HG02055.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.743+1571_743+1574d others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948318 | ||||||
| chr8:53948330
|
TAA | T | 12 | a0001c0001t0002g0106a0001c0001t0002g0232a0001c0001t0004g0011others(9): Show | 12 | HG01070.hp2 HG01071.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.743+1583_743+1584d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948330 | ||||||
| chr8:53948341
|
A | G | 1 | a0001c0001t0002g0182 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.743+1593A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948341 | ||||||
| chr8:53948364
|
GAC | G | 3 | a0001c0001t0001g0014a0001c0001t0001g0041a0001c0001t0001g0068 | 3 | HG00438.hp2 HG03453.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.743+1620_743+1621d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948364 | |||||
| chr8:53948366
|
C | T | 3 | a0001c0001t0005g0118a0001c0001t0005g0119a0001c0003t0002g0025 | 3 | HG02055.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.743+1618C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948366 | ||||||
| chr8:53948381
|
T | C | 6 | a0001c0001t0001g0015a0001c0001t0001g0252a0001c0001t0002g0108others(3): Show | 6 | HG00438.hp1 HG02055.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.743+1633T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948381 | ||||||
| chr8:53948399
|
T | C | 142 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(139): Show | 142 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.743+1651T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948399 | ||||||
| chr8:53948404
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.743+1656T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948404 | ||||||
| chr8:53948412
|
T | C | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+1664T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948412 | ||||||
| chr8:53948414
|
C | T | 59 | a0001c0001t0001g0014a0001c0001t0001g0093a0001c0001t0001g0105others(56): Show | 59 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.743+1666C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948414 | ||||||
| chr8:53948429
|
AGATACAG others(24): Show |
A | 1 | a0001c0001t0002g0200 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.743+1784_743+1814d others(33): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948429 | |||||
| chr8:53948437
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.743+1689T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948437 | ||||||
| chr8:53948445
|
T | C | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+1697T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948445 | ||||||
| chr8:53948447
|
C | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+1699C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948447 | ||||||
| chr8:53948460
|
T | A | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+1712T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948460 | ||||||
| chr8:53948460
|
T | TAA | 5 | a0001c0001t0002g0106a0001c0001t0002g0232a0001c0001t0005g0119others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.743+1712_743+1713i others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948460 | ||||||
| chr8:53948532
|
T | C | 1 | a0001c0001t0002g0190 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.743+1784T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948532 | ||||||
| chr8:53948532
|
T | TATATTTA others(24): Show |
1 | a0001c0001t0002g0073 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.743+1868_743+1898d others(33): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948532 | |||||
| chr8:53948532
|
TATATTTA others(24): Show |
T | 7 | a0001c0001t0001g0163a0001c0001t0002g0117a0001c0001t0002g0157others(4): Show | 7 | HG01358.hp2 HG02280.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.743+1868_743+1898d others(33): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948532 | |||||
| chr8:53948553
|
T | TGATACAG others(57): Show |
1 | a0001c0001t0002g0247 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.743+1814_743+1815i others(66): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948553 | |||||
| chr8:53948563
|
C | T | 202 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(199): Show | 202 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.743+1815C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948563 | ||||||
| chr8:53948584
|
T | A | 2 | a0001c0001t0002g0247a0001c0001t0003g0030 | 2 | HG02273.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.743+1836T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948584 | ||||||
| chr8:53948584
|
T | TAA | 3 | a0001c0001t0002g0159a0001c0001t0002g0244a0001c0003t0002g0025 | 3 | HG01346.hp1 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.743+1836_743+1837i others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948584 | ||||||
| chr8:53948594
|
C | T | 190 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0023others(187): Show | 190 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.743+1846C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948594 | ||||||
| chr8:53948602
|
C | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+1854C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948602 | ||||||
| chr8:53948610
|
ATATATGA others(55): Show |
A | 3 | a0001c0001t0001g0048a0001c0001t0003g0030a0001c0001t0004g0037 | 3 | HG01167.hp1 HG02630.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.743+1868_743+1929d others(64): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948610 | |||||
| chr8:53948615
|
T | A | 8 | a0001c0001t0002g0159a0001c0001t0002g0244a0001c0001t0002g0247others(5): Show | 8 | HG01168.hp2 HG01169.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.743+1867T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948615 | ||||||
| chr8:53948615
|
T | TAA | 24 | a0001c0001t0001g0093a0001c0001t0001g0120a0001c0001t0001g0166others(21): Show | 24 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.743+1867_743+1868i others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948615 | ||||||
| chr8:53948615
|
TGATACAG others(88): Show |
T | 1 | a0001c0001t0005g0119 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.743+1898_743+1992d others(97): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948615 | |||||
| chr8:53948625
|
C | T | 50 | a0001c0001t0001g0069a0001c0001t0001g0093a0001c0001t0001g0105others(47): Show | 50 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.743+1877C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948625 | ||||||
| chr8:53948633
|
C | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+1885C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948633 | ||||||
| chr8:53948639
|
CTA | C | 25 | a0001c0001t0001g0093a0001c0001t0001g0120a0001c0001t0001g0166others(22): Show | 25 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.743+1898_743+1899d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948639 | |||||
| chr8:53948641
|
A | ATATAAGA others(22): Show |
1 | a0001c0001t0002g0247 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.743+1897_743+1898i others(31): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948641 | |||||
| chr8:53948641
|
A | ATATATGA others(86): Show |
1 | a0001c0001t0002g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.743+1898_743+1899i others(95): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948641 | |||||
| chr8:53948641
|
A | ATATATGA others(84): Show |
1 | a0001c0001t0011g0208 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.743+1898_743+1899i others(93): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948641 | |||||
| chr8:53948641
|
ATATATAA others(24): Show |
A | 20 | a0001c0001t0001g0061a0001c0001t0001g0086a0001c0001t0001g0115others(17): Show | 20 | HG01070.hp1 HG01099.hp1 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.743+2220_743+2250d others(33): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948641 | |||||
| chr8:53948641
|
ATATATAA others(55): Show |
A | 26 | a0001c0001t0001g0015a0001c0001t0001g0068a0001c0001t0001g0077others(23): Show | 26 | HG00323.hp1 HG00609.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.743+2189_743+2250d others(64): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948641 | |||||
| chr8:53948641
|
ATATATAA others(86): Show |
A | 54 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0041others(51): Show | 54 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.743+2158_743+2250d others(95): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948641 | |||||
| chr8:53948641
|
ATATATAA others(117): Show |
A | 4 | a0001c0001t0001g0065a0001c0001t0001g0090a0001c0001t0002g0132others(1): Show | 4 | HG02818.hp1 HG02896.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.743+2127_743+2250d others(2): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948641 | |||||
| chr8:53948641
|
ATATATAA others(148): Show |
A | 4 | a0001c0001t0001g0049a0001c0001t0002g0243a0001c0001t0002g0245others(1): Show | 4 | HG00609.hp2 HG02486.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.743+2096_743+2250d others(2): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948641 | |||||
| chr8:53948646
|
TAA | T | 26 | a0001c0001t0001g0069a0001c0001t0001g0123a0001c0001t0002g0016others(23): Show | 26 | HG00408.hp1 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.743+1899_743+1900d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948646 | ||||||
| chr8:53948648
|
A | T | 1 | a0001c0001t0011g0208 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.743+1900A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948648 | ||||||
| chr8:53948658
|
C | T | 6 | a0001c0001t0001g0105a0001c0001t0001g0163a0001c0001t0002g0133others(3): Show | 6 | HG00408.hp1 HG02055.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.743+1910C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948658 | ||||||
| chr8:53948666
|
C | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+1918C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948666 | ||||||
| chr8:53948672
|
C | CTA | 3 | a0001c0001t0002g0164a0001c0001t0002g0200a0001c0001t0011g0208 | 3 | HG00408.hp1 HG02109.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.743+1929_743+1930d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948672 | |||||
| chr8:53948674
|
ATATAAGA others(22): Show |
A | 6 | a0001c0001t0001g0069a0001c0001t0001g0123a0001c0001t0002g0106others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.743+1931_743+1959d others(31): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948674 | |||||
| chr8:53948674
|
ATATAAGA others(53): Show |
A | 3 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013 | 3 | HG03540.hp1 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.743+1931_743+1990d others(62): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948674 | |||||
| chr8:53948674
|
ATATAAGA others(115): Show |
A | 12 | a0001c0001t0002g0020a0001c0001t0002g0038a0001c0001t0002g0168others(9): Show | 12 | HG01192.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.743+1931_743+2052d others(2): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948674 | |||||
| chr8:53948674
|
ATATAAGA others(146): Show |
A | 1 | a0001c0001t0002g0108 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.743+1931_743+2083d others(2): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948674 | |||||
| chr8:53948679
|
A | T | 3 | a0001c0001t0002g0016a0001c0001t0002g0179a0001c0002t0002g0009 | 3 | HG02895.hp2 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.743+1931A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948679 | ||||||
| chr8:53948689
|
C | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+1941C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948689 | ||||||
| chr8:53948705
|
ATATAAGA others(84): Show |
A | 1 | a0001c0002t0002g0009 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.743+1962_743+2052d others(93): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948705 | |||||
| chr8:53948705
|
ATATAAGA others(115): Show |
A | 2 | a0001c0001t0002g0016a0001c0001t0002g0179 | 2 | HG02895.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.743+1962_743+2083d others(2): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948705 | |||||
| chr8:53948720
|
C | T | 2 | a0001c0001t0005g0119a0001c0003t0002g0025 | 2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.743+1972C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948720 | ||||||
| chr8:53948751
|
C | T | 2 | a0001c0001t0005g0119a0001c0003t0002g0025 | 2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.743+2003C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948751 | ||||||
| chr8:53948782
|
C | T | 1 | a0001c0001t0005g0119 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.743+2034C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948782 | ||||||
| chr8:53948790
|
C | T | 45 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0035others(42): Show | 45 | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.743+2042C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948790 | ||||||
| chr8:53948813
|
C | T | 34 | a0001c0001t0001g0031a0001c0001t0001g0035a0001c0001t0001g0036others(31): Show | 34 | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.743+2065C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948813 | ||||||
| chr8:53948821
|
C | T | 64 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0031others(61): Show | 64 | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.743+2073C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948821 | ||||||
| chr8:53948844
|
C | T | 78 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0031others(75): Show | 78 | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.743+2096C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948844 | ||||||
| chr8:53948852
|
C | T | 86 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0031others(83): Show | 86 | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.743+2104C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948852 | ||||||
| chr8:53948875
|
C | T | 150 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(147): Show | 150 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.743+2127C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948875 | ||||||
| chr8:53948883
|
C | CATATGCT others(24): Show |
1 | a0001c0001t0002g0032 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.743+2157_743+2158i others(33): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948883 | |||||
| chr8:53948883
|
C | CTATATAA others(18): Show |
1 | a0001c0001t0002g0094 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.743+2135_743+2136i others(27): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948883 | ||||||
| chr8:53948883
|
C | T | 157 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(154): Show | 157 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.743+2135C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948883 | ||||||
| chr8:53948906
|
C | T | 180 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(177): Show | 180 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.743+2158C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948906 | ||||||
| chr8:53948914
|
C | CATATGCT others(55): Show |
1 | a0001c0001t0002g0182 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.743+2188_743+2189i others(64): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948914 | |||||
| chr8:53948914
|
C | T | 201 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(198): Show | 201 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.743+2166C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948914 | ||||||
| chr8:53948937
|
C | T | 210 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(207): Show | 210 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.743+2189C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948937 | ||||||
| chr8:53948945
|
C | T | 210 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(207): Show | 210 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.743+2197C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948945 | ||||||
| chr8:53948968
|
C | CATATTTA others(24): Show |
1 | a0001c0001t0011g0208 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.743+2228_743+2258d others(33): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948968 | |||||
| chr8:53948968
|
C | T | 245 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(242): Show | 245 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.743+2220C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948968 | ||||||
| chr8:53948976
|
C | CATATGCT others(24): Show |
1 | a0001c0001t0002g0073 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.743+2450_743+2480d others(33): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948976 | |||||
| chr8:53948976
|
C | T | 235 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(232): Show | 235 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.743+2228C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948976 | ||||||
| chr8:53948976
|
CATATGCT others(55): Show |
C | 1 | a0001c0001t0002g0104 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.743+2419_743+2480d others(64): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948976 | |||||
| chr8:53948984
|
ATATAAGA others(22): Show |
A | 1 | a0001c0001t0001g0089 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.743+2241_743+2269d others(31): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948984 | |||||
| chr8:53948999
|
T | C | 2 | a0001c0001t0002g0217a0001c0001t0002g0251 | 2 | HG01099.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.743+2251T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948999 | ||||||
| chr8:53949007
|
T | C | 4 | a0001c0001t0002g0217a0001c0001t0002g0251a0001c0001t0005g0118others(1): Show | 4 | HG01099.hp2 HG01243.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.743+2259T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949007 | ||||||
| chr8:53949012
|
G | A | 4 | a0001c0001t0002g0094a0001c0001t0002g0134a0001c0001t0002g0182others(1): Show | 4 | HG00597.hp2 HG02280.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.743+2264G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949012 | ||||||
| chr8:53949013
|
C | CTATATAT others(28): Show |
2 | a0001c0001t0002g0134a0001c0001t0002g0182 | 2 | HG03942.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.743+2271_743+2272i others(37): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949013 | |||||
| chr8:53949015
|
ATATAAGA others(22): Show |
A | 1 | a0001c0001t0002g0210 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.743+2272_743+2300d others(31): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949015 | |||||
| chr8:53949030
|
T | C | 1 | a0001c0001t0002g0217 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.743+2282T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949030 | ||||||
| chr8:53949038
|
T | C | 1 | a0001c0001t0002g0217 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.743+2290T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949038 | ||||||
| chr8:53949043
|
G | A | 12 | a0001c0001t0002g0032a0001c0001t0002g0094a0001c0001t0002g0117others(9): Show | 12 | HG00597.hp2 HG00741.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.743+2295G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949043 | ||||||
| chr8:53949044
|
C | CTA | 14 | a0001c0001t0001g0089a0001c0001t0002g0032a0001c0001t0002g0094others(11): Show | 14 | HG00423.hp2 HG00597.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.743+2301_743+2302d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949044 | |||||
| chr8:53949044
|
C | CTATATAT others(28): Show |
1 | a0001c0001t0002g0203 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.743+2302_743+2303i others(37): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949044 | |||||
| chr8:53949046
|
ATATAAGA others(22): Show |
A | 3 | a0001c0001t0001g0198a0001c0001t0002g0154a0001c0001t0002g0258 | 3 | HG00642.hp1 HG01261.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.743+2303_743+2331d others(31): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949046 | |||||
| chr8:53949069
|
T | C | 2 | a0001c0001t0002g0104a0001c0001t0002g0217 | 2 | HG01243.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.743+2321T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949069 | ||||||
| chr8:53949074
|
G | A | 32 | a0001c0001t0001g0093a0001c0001t0001g0163a0001c0001t0001g0166others(29): Show | 32 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.743+2326G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949074 | ||||||
| chr8:53949075
|
C | CTA | 30 | a0001c0001t0001g0066a0001c0001t0001g0071a0001c0001t0001g0081others(27): Show | 30 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.743+2332_743+2333d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949075 | |||||
| chr8:53949075
|
C | CTATATAT others(28): Show |
11 | a0001c0001t0001g0093a0001c0001t0002g0129a0001c0001t0002g0133others(8): Show | 11 | HG00639.hp1 HG01109.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.743+2333_743+2334i others(37): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949075 | |||||
| chr8:53949077
|
ATATAAGA others(22): Show |
A | 23 | a0001c0001t0001g0031a0001c0001t0001g0035a0001c0001t0001g0036others(20): Show | 23 | HG00597.hp1 HG01074.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.743+2334_743+2362d others(31): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949077 | |||||
| chr8:53949105
|
G | A | 56 | a0001c0001t0001g0023a0001c0001t0001g0055a0001c0001t0001g0089others(53): Show | 56 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.743+2357G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949105 | ||||||
| chr8:53949106
|
C | CTA | 54 | a0001c0001t0001g0048a0001c0001t0001g0055a0001c0001t0001g0061others(51): Show | 54 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.743+2363_743+2364d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949106 | |||||
| chr8:53949106
|
C | CTATATAT others(28): Show |
3 | a0001c0001t0001g0105a0001c0001t0001g0120a0001c0001t0001g0229 | 3 | NA18988.hp2 NA19077.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.743+2364_743+2365i others(37): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949106 | |||||
| chr8:53949106
|
C | CTATATAT others(61): Show |
1 | a0001c0001t0002g0164 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.743+2364_743+2365i others(70): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949106 | |||||
| chr8:53949108
|
ATATAAGA others(22): Show |
A | 13 | a0001c0001t0001g0023a0001c0001t0002g0192a0001c0001t0003g0001others(10): Show | 13 | HG01257.hp1 HG01891.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.743+2365_743+2393d others(31): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949108 | |||||
| chr8:53949136
|
G | A | 82 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0001g0040others(79): Show | 82 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.743+2388G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949136 | ||||||
| chr8:53949137
|
C | CTA | 95 | a0001c0001t0001g0018a0001c0001t0001g0031a0001c0001t0001g0035others(92): Show | 95 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.743+2394_743+2395d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949137 | |||||
| chr8:53949137
|
C | CTATATAT others(28): Show |
1 | a0001c0001t0001g0081 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.743+2395_743+2396i others(37): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949137 | |||||
| chr8:53949139
|
ATATAAGA others(22): Show |
A | 12 | a0001c0001t0001g0068a0001c0001t0001g0077a0001c0001t0001g0121others(9): Show | 12 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.743+2396_743+2424d others(31): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949139 | |||||
| chr8:53949167
|
G | A | 124 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0036others(121): Show | 124 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.743+2419G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949167 | ||||||
| chr8:53949168
|
C | CTA | 189 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(186): Show | 189 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.743+2425_743+2426d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949168 | |||||
| chr8:53949168
|
C | CTATATAT others(61): Show |
1 | a0001c0001t0001g0222 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.743+2426_743+2427i others(70): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949168 | |||||
| chr8:53949170
|
ATATAAGA others(22): Show |
A | 1 | a0001c0005t0002g0113 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.743+2427_743+2455d others(31): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949170 | |||||
| chr8:53949198
|
G | A | 152 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0023others(149): Show | 152 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.743+2450G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949198 | ||||||
| chr8:53949199
|
C | CTA | 205 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(202): Show | 205 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.743+2456_743+2457d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949199 | |||||
| chr8:53949199
|
C | CTATATAA others(191): Show |
1 | a0001c0001t0002g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.743+2571_743+2572i others(200): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949199 | |||||
| chr8:53949199
|
C | CTATATAA others(191): Show |
1 | a0001c0001t0011g0208 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.743+2483_743+2484i others(200): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949199 | |||||
| chr8:53949199
|
C | CTATATAA others(26): Show |
1 | a0001c0001t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.743+2480_743+2481i others(35): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949199 | |||||
| chr8:53949199
|
C | CTATATAT others(28): Show |
2 | a0001c0001t0001g0256a0001c0001t0003g0022 | 2 | HG03471.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.743+2457_743+2458i others(37): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949199 | |||||
| chr8:53949199
|
C | CTATATAT others(61): Show |
3 | a0001c0001t0002g0159a0001c0001t0002g0199a0001c0001t0002g0247 | 3 | HG01346.hp1 HG02273.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.743+2457_743+2458i others(70): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949199 | |||||
| chr8:53949199
|
CTATATAA others(26): Show |
C | 1 | a0001c0001t0002g0135 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.743+2539_743+2571d others(35): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949199 | |||||
| chr8:53949229
|
A | G | 25 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0042others(22): Show | 25 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.743+2481A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949229 | ||||||
| chr8:53949236
|
A | G | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+2488A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949236 | ||||||
| chr8:53949250
|
A | C | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+2502A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949250 | ||||||
| chr8:53949262
|
A | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0049a0001c0001t0001g0074others(1): Show | 4 | HG00609.hp2 HG01496.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.743+2514A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949262 | ||||||
| chr8:53949269
|
A | G | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+2521A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949269 | ||||||
| chr8:53949283
|
A | C | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+2535A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949283 | ||||||
| chr8:53949295
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.743+2547A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949295 | ||||||
| chr8:53949404
|
A | T | 2 | a0001c0001t0002g0227a0001c0001t0002g0228 | 2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.743+2656A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949404 | ||||||
| chr8:53949418
|
A | G | 1 | a0001c0005t0002g0113 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.743+2670A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949418 | ||||||
| chr8:53949425
|
A | G | 1 | a0001c0001t0001g0115 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.743+2677A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949425 | ||||||
| chr8:53949542
|
C | T | 2 | a0001c0001t0006g0043a0001c0001t0006g0044 | 2 | HG01069.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.743+2794C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949542 | ||||||
| chr8:53949572
|
G | A | 1 | a0001c0001t0001g0120 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.743+2824G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949572 | ||||||
| chr8:53949718
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.743+2970A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949718 | ||||||
| chr8:53949845
|
C | CT | 141 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(138): Show | 141 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.743+3109dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949845 | |||||
| chr8:53949874
|
C | G | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+3126C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949874 | ||||||
| chr8:53950130
|
A | G | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+3382A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53950130 | ||||||
| chr8:53950172
|
A | G | 1 | a0001c0001t0001g0050 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.743+3424A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53950172 | ||||||
| chr8:53950376
|
C | T | 4 | a0001c0001t0002g0235a0001c0001t0005g0118a0001c0001t0005g0119others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.743+3628C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53950376 | ||||||
| chr8:53950441
|
G | A | 182 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(179): Show | 182 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.744-3635G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53950441 | ||||||
| chr8:53950620
|
GT | G | 8 | a0001c0001t0001g0112a0001c0001t0001g0116a0001c0001t0001g0197others(5): Show | 8 | HG00323.hp2 HG01109.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.744-3443delT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53950620 | |||||
| chr8:53950836
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.744-3240A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53950836 | ||||||
| chr8:53950853
|
G | A | 2 | a0001c0001t0005g0118a0001c0001t0005g0119 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.744-3223G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53950853 | ||||||
| chr8:53950933
|
C | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.744-3143C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53950933 | ||||||
| chr8:53951348
|
C | T | 6 | a0001c0001t0002g0106a0001c0001t0002g0232a0001c0001t0004g0037others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.744-2728C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53951348 | ||||||
| chr8:53951405
|
A | G | 2 | a0001c0001t0003g0030a0001c0001t0003g0170 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.744-2671A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53951405 | ||||||
| chr8:53951888
|
C | G | 3 | a0001c0001t0005g0118a0001c0001t0005g0119a0001c0003t0002g0025 | 3 | HG02055.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.744-2188C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53951888 | ||||||
| chr8:53951909
|
C | T | 1 | a0001c0001t0002g0185 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.744-2167C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53951909 | ||||||
| chr8:53951973
|
C | T | 1 | a0001c0001t0002g0257 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.744-2103C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53951973 | ||||||
| chr8:53952171
|
G | A | 12 | a0001c0001t0001g0041a0001c0001t0001g0065a0001c0001t0001g0068others(9): Show | 12 | HG00438.hp2 HG02165.hp2 NA18612.hp2 others(9): Show |
intron_variant | MODIFIER | c.744-1905G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53952171 | ||||||
| chr8:53952244
|
A | AT | 43 | a0001c0001t0001g0015a0001c0001t0001g0048a0001c0001t0001g0076others(40): Show | 43 | HG00639.hp2 HG01109.hp2 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.744-1811dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53952244 | |||||
| chr8:53952244
|
A | ATT | 6 | a0001c0001t0002g0020a0001c0001t0002g0168a0001c0001t0002g0196others(3): Show | 6 | HG01109.hp1 HG02486.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.744-1812_744-1811d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53952244 | |||||
| chr8:53952244
|
AT | A | 13 | a0001c0001t0002g0106a0001c0001t0002g0232a0001c0001t0002g0236others(10): Show | 13 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.744-1811delT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53952244 | |||||
| chr8:53952297
|
C | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.744-1779C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53952297 | ||||||
| chr8:53952483
|
C | T | 6 | a0001c0001t0002g0131a0001c0001t0002g0139a0001c0001t0002g0185others(3): Show | 6 | HG01070.hp1 HG01975.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.744-1593C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53952483 | ||||||
| chr8:53952590
|
G | A | 181 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(178): Show | 181 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.744-1486G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53952590 | ||||||
| chr8:53952657
|
C | T | 2 | a0001c0001t0003g0030a0001c0001t0003g0170 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.744-1419C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53952657 | ||||||
| chr8:53952681
|
G | A | 120 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(117): Show | 120 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.744-1395G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53952681 | ||||||
| chr8:53952864
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.744-1212T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53952864 | ||||||
| chr8:53952876
|
G | A | 1 | a0001c0001t0002g0149 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.744-1200G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53952876 | ||||||
| chr8:53952969
|
T | G | 2 | a0001c0001t0001g0069a0001c0001t0001g0123 | 2 | NA18945.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.744-1107T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53952969 | ||||||
| chr8:53952972
|
A | G | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.744-1104A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53952972 | ||||||
| chr8:53953300
|
C | A | 1 | a0001c0001t0001g0222 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.744-776C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53953300 | ||||||
| chr8:53953484
|
G | T | 1 | a0001c0001t0009g0136 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.744-592G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53953484 | ||||||
| chr8:53953520
|
C | CA | 215 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.744-544dupA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53953520 | |||||
| chr8:53953588
|
C | T | 167 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(164): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.744-488C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53953588 | ||||||
| chr8:53953622
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.744-454T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53953622 | ||||||
| chr8:53953931
|
C | A | 167 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(164): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.744-145C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53953931 | ||||||
| chr8:53954430
|
G | T | 1 | a0001c0001t0002g0191 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.978+120G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53954430 | ||||||
| chr8:53954489
|
C | T | 1 | a0001c0001t0002g0131 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.978+179C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53954489 | ||||||
| chr8:53954689
|
CT | C | 45 | a0001c0001t0001g0059a0001c0001t0002g0094a0001c0001t0002g0117others(42): Show | 45 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.978+395delT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 53954689 | |||||
| chr8:53954716
|
C | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.978+406C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53954716 | ||||||
| chr8:53954727
|
G | A | 21 | a0001c0001t0002g0016a0001c0001t0002g0020a0001c0001t0002g0038others(18): Show | 21 | HG01192.hp2 HG01891.hp1 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.978+417G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53954727 | ||||||
| chr8:53954845
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.978+535G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53954845 | ||||||
| chr8:53954982
|
G | A | 1 | a0001c0001t0002g0215 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.978+672G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53954982 | ||||||
| chr8:53955057
|
C | T | 4 | a0001c0001t0002g0133a0001c0001t0006g0043a0001c0001t0006g0044others(1): Show | 4 | HG01069.hp2 HG02630.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.978+747C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53955057 | ||||||
| chr8:53955209
|
T | C | 54 | a0001c0001t0002g0016a0001c0001t0002g0020a0001c0001t0002g0021others(51): Show | 54 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.978+899T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53955209 | ||||||
| chr8:53955499
|
T | C | 2 | a0001c0001t0009g0128a0001c0001t0009g0136 | 2 | HG04184.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.978+1189T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53955499 | ||||||
| chr8:53955612
|
C | G | 2 | a0001c0001t0002g0196a0001c0001t0002g0240 | 2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.978+1302C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53955612 | ||||||
| chr8:53955721
|
C | T | 35 | a0001c0001t0001g0031a0001c0001t0001g0035a0001c0001t0001g0036others(32): Show | 35 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.978+1411C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53955721 | ||||||
| chr8:53955787
|
C | T | 1 | a0001c0001t0002g0108 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.978+1477C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53955787 | ||||||
| chr8:53955913
|
T | C | 124 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(121): Show | 124 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.978+1603T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53955913 | ||||||
| chr8:53955938
|
G | A | 54 | a0001c0001t0002g0016a0001c0001t0002g0020a0001c0001t0002g0021others(51): Show | 54 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.978+1628G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53955938 | ||||||
| chr8:53956239
|
G | C | 7 | a0001c0001t0002g0020a0001c0001t0002g0038a0001c0001t0002g0108others(4): Show | 7 | HG01891.hp1 HG02572.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.978+1929G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53956239 | ||||||
| chr8:53956246
|
A | G | 178 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(175): Show | 178 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.978+1936A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53956246 | ||||||
| chr8:53956264
|
A | T | 2 | a0001c0001t0002g0021a0001c0001t0011g0208 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.978+1954A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53956264 | ||||||
| chr8:53956471
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.979-1799G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53956471 | ||||||
| chr8:53956490
|
A | C | 15 | a0001c0001t0002g0106a0001c0001t0002g0176a0001c0001t0002g0232others(12): Show | 15 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.979-1780A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53956490 | ||||||
| chr8:53956592
|
T | A | 1 | a0001c0001t0002g0182 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.979-1678T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53956592 | ||||||
| chr8:53956643
|
C | T | 1 | a0001c0001t0002g0244 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.979-1627C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53956643 | ||||||
| chr8:53956730
|
T | A | 1 | a0001c0001t0002g0094 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.979-1540T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53956730 | ||||||
| chr8:53956905
|
T | C | 1 | a0001c0002t0003g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.979-1365T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53956905 | ||||||
| chr8:53956913
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.979-1357C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53956913 | ||||||
| chr8:53957124
|
A | ATTTTG | 15 | a0001c0001t0003g0001a0001c0001t0003g0024a0001c0001t0003g0030others(12): Show | 15 | HG01168.hp2 HG01169.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.979-1131_979-1127d others(7): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 53957124 | |||||
| chr8:53957320
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.979-950G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53957320 | ||||||
| chr8:53957393
|
G | C | 55 | a0001c0001t0002g0016a0001c0001t0002g0020a0001c0001t0002g0021others(52): Show | 55 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.979-877G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53957393 | ||||||
| chr8:53957442
|
T | C | 7 | a0001c0001t0002g0053a0001c0001t0002g0070a0001c0001t0002g0167others(4): Show | 7 | HG01099.hp1 HG01496.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.979-828T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53957442 | ||||||
| chr8:53957498
|
C | G | 1 | a0001c0001t0001g0166 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.979-772C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53957498 | ||||||
| chr8:53957675
|
T | C | 1 | a0001c0005t0002g0113 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.979-595T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53957675 | ||||||
| chr8:53957783
|
T | C | 3 | a0001c0001t0001g0046a0001c0001t0001g0095a0001c0001t0001g0186 | 3 | HG00621.hp1 HG02040.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.979-487T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53957783 | ||||||
| chr8:53957823
|
T | C | 1 | a0001c0001t0001g0166 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.979-447T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53957823 | ||||||
| chr8:53957945
|
G | A | 2 | a0001c0001t0002g0129a0001c0001t0002g0160 | 2 | NA18955.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.979-325G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53957945 | ||||||
| chr8:53958168
|
A | C | 1 | a0001c0001t0002g0124 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.979-102A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53958168 | ||||||
| chr8:53958206
|
A | T | 1 | a0001c0001t0001g0090 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.979-64A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53958206 |