| geneid | 26166 |
|---|---|
| ensemblid | ENSG00000132554.21 |
| hgncid | 24499 |
| symbol | RGS22 |
| name | regulator of G protein signaling 22 |
| refseq_nuc | NM_015668.5 |
| refseq_prot | NP_056483.3 |
| ensembl_nuc | ENST00000360863.11 |
| ensembl_prot | ENSP00000354109.6 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 99960936 |
| end | 100106049 |
| strand | - |
| ver | v1.2 |
| region | chr8:99960936-100106049 |
| region5000 | chr8:99955936-100111049 |
| regionname0 | RGS22_chr8_99960936_100106049 |
| regionname5000 | RGS22_chr8_99955936_100111049 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000 | 0/0 | 0 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0001 | 1/1 | 1264 | 249 | 57 | 49 | 103 | 8 | 30 | 76 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0002 | 0/0 | 1264 | 24 | 1 | 1 | 19 | 0 | 3 | 16 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0003 | 0/0 | 1264 | 15 | 15 | 0 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0004 | 0/0 | 1264 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0005 | 0/0 | 1264 | 3 | 0 | 1 | 2 | 0 | 0 | 2 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0006 | 0/0 | 1264 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0007 | 0/0 | 1264 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0008 | 0/0 | 1264 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0009 | 0/0 | 1264 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0010 | 0/0 | 1264 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0011 | 0/0 | 1264 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0012 | 0/0 | 1264 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0013 | 0/0 | 1264 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0014 | 0/0 | 1264 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0015 | 0/0 | 1264 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0016 | 0/0 | 1264 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| 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 | 3795 | 209 | 27 | 46 | 97 | 8 | 29 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| c0002 | 0/0 | 3795 | 22 | 1 | 1 | 18 | 0 | 2 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| c0003 | 0/0 | 3795 | 20 | 13 | 0 | 6 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| c0004 | 0/0 | 3795 | 15 | 12 | 3 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| c0005 | 0/0 | 3795 | 14 | 14 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| c0006 | 0/0 | 3795 | 3 | 0 | 1 | 2 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| c0007 | 0/0 | 3795 | 3 | 3 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| c0008 | 0/0 | 3795 | 3 | 0 | 0 | 3 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| c0009 | 0/0 | 3795 | 2 | 2 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| c0010 | 0/0 | 3795 | 2 | 0 | 0 | 2 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| c0011 | 0/0 | 3795 | 2 | 0 | 0 | 1 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| c0012 | 0/0 | 3795 | 2 | 2 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| c0013 | 0/0 | 3795 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| c0014 | 0/0 | 3795 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| c0015 | 0/0 | 3795 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| c0016 | 0/0 | 3795 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| c0017 | 0/0 | 3795 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| c0018 | 0/0 | 3795 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| c0019 | 0/0 | 3795 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| c0020 | 0/0 | 3795 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| c0021 | 0/0 | 3795 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| c0022 | 0/0 | 3795 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| c0023 | 0/0 | 3795 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| c0024 | 0/0 | 3795 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| c0025 | 0/0 | 3795 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| 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 | 1/1 | 435 | 291 | 66 | 48 | 134 | 8 | 33 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| t0002 | 0/0 | 435 | 15 | 12 | 3 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| t0003 | 0/0 | 435 | 2 | 1 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| t0004 | 0/0 | 435 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| t0005 | 0/0 | 435 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0226 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0288 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0019 | 0/0 | 3795 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0000c0021 | 0/0 | 3795 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0001c0001 | 1/1 | 3795 | 209 | 27 | 46 | 97 | 8 | 29 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0001c0003 | 0/0 | 3795 | 20 | 13 | 0 | 6 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0001c0004 | 0/0 | 3795 | 15 | 12 | 3 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0001c0009 | 0/0 | 3795 | 2 | 2 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0001c0012 | 0/0 | 3795 | 2 | 2 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0001c0024 | 0/0 | 3795 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0002c0002 | 0/0 | 3795 | 22 | 1 | 1 | 18 | 0 | 2 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0002c0011 | 0/0 | 3795 | 2 | 0 | 0 | 1 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0003c0005 | 0/0 | 3795 | 14 | 14 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0003c0022 | 0/0 | 3795 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0004c0008 | 0/0 | 3795 | 3 | 0 | 0 | 3 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0005c0006 | 0/0 | 3795 | 3 | 0 | 1 | 2 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0006c0007 | 0/0 | 3795 | 3 | 3 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0007c0010 | 0/0 | 3795 | 2 | 0 | 0 | 2 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0008c0013 | 0/0 | 3795 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0009c0014 | 0/0 | 3795 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0010c0015 | 0/0 | 3795 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0011c0016 | 0/0 | 3795 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0012c0023 | 0/0 | 3795 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0013c0020 | 0/0 | 3795 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0014c0018 | 0/0 | 3795 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0015c0017 | 0/0 | 3795 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0016c0025 | 0/0 | 3795 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0019t0001 | 0/0 | 4229 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0000c0021t0001 | 0/0 | 4229 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0001c0001t0001 | 1/1 | 4229 | 207 | 27 | 45 | 97 | 8 | 28 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0001c0001t0003 | 0/0 | 4229 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0001c0001t0004 | 0/0 | 4229 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0001c0003t0001 | 0/0 | 4229 | 20 | 13 | 0 | 6 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0001c0004t0002 | 0/0 | 4229 | 14 | 11 | 3 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0001c0004t0005 | 0/0 | 4229 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0001c0009t0001 | 0/0 | 4229 | 2 | 2 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0001c0012t0001 | 0/0 | 4229 | 2 | 2 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0001c0024t0001 | 0/0 | 4229 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0002c0002t0001 | 0/0 | 4229 | 22 | 1 | 1 | 18 | 0 | 2 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0002c0011t0001 | 0/0 | 4229 | 2 | 0 | 0 | 1 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0003c0005t0001 | 0/0 | 4229 | 14 | 14 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0003c0022t0002 | 0/0 | 4229 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0004c0008t0001 | 0/0 | 4229 | 3 | 0 | 0 | 3 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0005c0006t0001 | 0/0 | 4229 | 3 | 0 | 1 | 2 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0006c0007t0001 | 0/0 | 4229 | 3 | 3 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0007c0010t0001 | 0/0 | 4229 | 2 | 0 | 0 | 2 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0008c0013t0001 | 0/0 | 4229 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0009c0014t0001 | 0/0 | 4229 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0010c0015t0001 | 0/0 | 4229 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0011c0016t0001 | 0/0 | 4229 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0012c0023t0003 | 0/0 | 4229 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0013c0020t0001 | 0/0 | 4229 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0014c0018t0001 | 0/0 | 4229 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0015c0017t0001 | 0/0 | 4229 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| a0016c0025t0001 | 0/0 | 4229 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | copy fasta | chr8 | 99955936 | 100111049 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0019t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0000c0021t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0226 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0288 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0003g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0003t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0003t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0003t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0003t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0003t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0003t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0003t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0003t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0003t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0003t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0003t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0004t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0004t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0004t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0004t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0004t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0004t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0004t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0004t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0004t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0004t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0004t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0004t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0004t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0004t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0004t0005g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0009t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0009t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0012t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0012t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0001c0024t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0002c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0002c0011t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0002c0011t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0003c0005t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0003c0005t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0003c0005t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0003c0005t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0003c0005t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0003c0005t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0003c0005t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0003c0005t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0003c0005t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0003c0005t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0003c0005t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0003c0005t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0003c0005t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0003c0022t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0004c0008t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0004c0008t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0004c0008t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0005c0006t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0005c0006t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0005c0006t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0006c0007t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0006c0007t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0006c0007t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0007c0010t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0007c0010t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0008c0013t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0009c0014t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0010c0015t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0011c0016t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0012c0023t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0013c0020t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0014c0018t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0015c0017t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| a0016c0025t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | GBR | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0198 | EUR | GBR | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0156 | EAS | CHS | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | CHS | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | CHS | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG00673 | hp1 | a0000 | c0019 | t0001 | g0248 | EAS | CHS | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG00673 | hp2 | a0000 | c0021 | t0001 | g0150 | EAS | CHS | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG00733 | hp1 | a0001 | c0004 | t0002 | g0115 | AMR | PUR | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG00738 | hp2 | a0001 | c0004 | t0002 | g0116 | AMR | PUR | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01081 | hp1 | a0005 | c0006 | t0001 | g0082 | AMR | PUR | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01175 | hp1 | a0013 | c0020 | t0001 | g0279 | AMR | PUR | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01243 | hp1 | a0001 | c0004 | t0002 | g0120 | AMR | PUR | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | IBS | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0203 | EUR | IBS | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01884 | hp1 | a0001 | c0004 | t0002 | g0114 | AFR | ACB | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01884 | hp2 | a0006 | c0007 | t0001 | g0113 | AFR | ACB | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0033 | AMR | PEL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PEL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0153 | EAS | KHV | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02145 | hp1 | a0001 | c0003 | t0001 | g0076 | AFR | ACB | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02145 | hp2 | a0001 | c0012 | t0001 | g0112 | AFR | ACB | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | CDX | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CDX | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02257 | hp1 | a0001 | c0004 | t0002 | g0053 | AFR | ACB | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02257 | hp2 | a0001 | c0003 | t0001 | g0239 | AFR | ACB | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02280 | hp1 | a0003 | c0005 | t0001 | g0059 | AFR | ACB | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0075 | AFR | ACB | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02451 | hp1 | a0001 | c0024 | t0001 | g0299 | AFR | ACB | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02451 | hp2 | a0003 | c0022 | t0002 | g0110 | AFR | ACB | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02572 | hp2 | a0001 | c0009 | t0001 | g0100 | AFR | GWD | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02615 | hp1 | a0001 | c0004 | t0002 | g0121 | AFR | GWD | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0130 | AFR | GWD | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0064 | AFR | GWD | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02717 | hp1 | a0003 | c0005 | t0001 | g0069 | AFR | GWD | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02723 | hp1 | a0001 | c0004 | t0002 | g0124 | AFR | GWD | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02735 | hp1 | a0002 | c0011 | t0001 | g0071 | SAS | PJL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | PJL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02809 | hp1 | a0003 | c0005 | t0001 | g0108 | AFR | GWD | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02809 | hp2 | a0001 | c0004 | t0005 | g0308 | AFR | GWD | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02818 | hp1 | a0012 | c0023 | t0003 | g0105 | AFR | GWD | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02895 | hp2 | a0001 | c0004 | t0002 | g0062 | AFR | GWD | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02897 | hp1 | a0001 | c0004 | t0002 | g0063 | AFR | GWD | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ESN | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02965 | hp1 | a0001 | c0004 | t0002 | g0123 | AFR | ESN | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02965 | hp2 | a0003 | c0005 | t0001 | g0107 | AFR | ESN | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0077 | AFR | ESN | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0289 | AFR | ESN | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03041 | hp2 | a0003 | c0005 | t0001 | g0057 | AFR | GWD | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03098 | hp2 | a0001 | c0004 | t0002 | g0127 | AFR | MSL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03139 | hp2 | a0003 | c0005 | t0001 | g0002 | AFR | ESN | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03195 | hp1 | a0001 | c0004 | t0002 | g0122 | AFR | ESN | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03195 | hp2 | a0003 | c0005 | t0001 | g0109 | AFR | ESN | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03209 | hp1 | a0001 | c0012 | t0001 | g0131 | AFR | MSL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03209 | hp2 | a0001 | c0004 | t0002 | g0119 | AFR | MSL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03225 | hp1 | a0001 | c0003 | t0001 | g0052 | AFR | MSL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03225 | hp2 | a0011 | c0016 | t0001 | g0132 | AFR | MSL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0056 | AFR | MSL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03453 | hp2 | a0003 | c0005 | t0001 | g0060 | AFR | MSL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0055 | AFR | MSL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03540 | hp1 | a0010 | c0015 | t0001 | g0117 | AFR | GWD | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03579 | hp2 | a0003 | c0005 | t0001 | g0061 | AFR | MSL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0259 | SAS | PJL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | BEB | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | BEB | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | BEB | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0142 | SAS | STU | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | STU | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | BEB | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0133 | SAS | BEB | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | STU | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | STU | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | STU | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG04228 | hp2 | a0009 | c0014 | t0001 | g0146 | SAS | STU | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHB | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18612 | hp2 | a0001 | c0003 | t0001 | g0079 | EAS | CHB | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18747 | hp1 | a0001 | c0003 | t0001 | g0078 | EAS | CHB | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0151 | EAS | CHB | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18906 | hp1 | a0003 | c0005 | t0001 | g0095 | AFR | YRI | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | YRI | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18950 | hp2 | a0001 | c0003 | t0001 | g0080 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18962 | hp1 | a0001 | c0003 | t0001 | g0140 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18963 | hp1 | a0016 | c0025 | t0001 | g0307 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18966 | hp2 | a0005 | c0006 | t0001 | g0092 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18968 | hp2 | a0007 | c0010 | t0001 | g0291 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18970 | hp1 | a0004 | c0008 | t0001 | g0189 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18991 | hp1 | a0014 | c0018 | t0001 | g0148 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18992 | hp2 | a0001 | c0003 | t0001 | g0264 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19001 | hp1 | a0001 | c0003 | t0001 | g0214 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19030 | hp1 | a0003 | c0005 | t0001 | g0094 | AFR | LWK | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19030 | hp2 | a0006 | c0007 | t0001 | g0125 | AFR | LWK | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | LWK | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0001 | AFR | LWK | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19058 | hp1 | a0015 | c0017 | t0001 | g0046 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19068 | hp1 | a0004 | c0008 | t0001 | g0173 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19082 | hp1 | a0002 | c0011 | t0001 | g0147 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19085 | hp1 | a0005 | c0006 | t0001 | g0091 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19087 | hp1 | a0004 | c0008 | t0001 | g0191 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19090 | hp2 | a0007 | c0010 | t0001 | g0171 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | YRI | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0074 | AFR | YRI | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ASW | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA20129 | hp2 | a0008 | c0013 | t0001 | g0089 | AFR | ASW | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0243 | EUR | TSI | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0241 | EUR | TSI | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0219 | EUR | TSI | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | TSI | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | GIH | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA20905 | hp2 | a0001 | c0003 | t0001 | g0009 | SAS | GIH | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02109 | hp1 | a0001 | c0004 | t0002 | g0054 | AFR | ACB | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02486 | hp1 | a0003 | c0005 | t0001 | g0002 | AFR | ACB | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02486 | hp2 | a0001 | c0009 | t0001 | g0101 | AFR | ACB | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG02559 | hp2 | a0003 | c0005 | t0001 | g0068 | AFR | ACB | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0005 | AFR | MSL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | USA | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| HG06807 | hp2 | a0006 | c0007 | t0001 | g0126 | AFR | USA | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | USA | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA20300 | hp2 | a0003 | c0005 | t0001 | g0106 | AFR | USA | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | LWK | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| NA21309 | hp2 | a0001 | c0003 | t0001 | g0001 | AFR | LWK | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0226 | REF | REF | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0288 | REF | REF | RGS22_chr8_99955936_100111049 | RGS22 | chr8 | 99955936 | 100111049 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:99962441
|
A | G | 1 | a0000 | 2 | HG00673.hp1 HG00673.hp2 |
stop_lost&splice_region_variant | HIGH | c.3793T>C | p.Ter1265Argext*? | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 27/28 | 3921/4229 | 3793/3795 | 1265/1264 | chr8 | 99962441 | ||
| chr8:99981944
|
T | C | 1 | a0013 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.3353A>G | p.Glu1118Gly | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/28 | 3481/4229 | 3353/3795 | 1118/1264 | chr8 | 99981944 | ||
| chr8:99981975
|
G | C | 1 | a0007 | 2 | NA18968.hp2 NA19090.hp2 |
missense_variant | MODERATE | c.3322C>G | p.Arg1108Gly | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/28 | 3450/4229 | 3322/3795 | 1108/1264 | chr8 | 99981975 | ||
| chr8:99982093
|
A | C | 1 | a0006 | 3 | HG01884.hp2 HG06807.hp2 NA19030.hp2 |
missense_variant | MODERATE | c.3204T>G | p.Asp1068Glu | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/28 | 3332/4229 | 3204/3795 | 1068/1264 | chr8 | 99982093 | ||
| chr8:99999366
|
G | A | 1 | a0012 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.2845C>T | p.Pro949Ser | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 19/28 | 2973/4229 | 2845/3795 | 949/1264 | chr8 | 99999366 | ||
| chr8:99999384
|
G | A | 4 | a0000a0002a0005others(1): Show | 29 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(26): Show |
missense_variant | MODERATE | c.2827C>T | p.His943Tyr | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 19/28 | 2955/4229 | 2827/3795 | 943/1264 | chr8 | 99999384 | ||
| chr8:100004023
|
C | T | 1 | a0005 | 3 | HG01081.hp1 NA18966.hp2 NA19085.hp1 |
missense_variant | MODERATE | c.2530G>A | p.Val844Ile | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 17/28 | 2658/4229 | 2530/3795 | 844/1264 | chr8 | 100004023 | ||
| chr8:100038945
|
A | G | 1 | a0010 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.2152T>C | p.Cys718Arg | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/28 | 2280/4229 | 2152/3795 | 718/1264 | chr8 | 100038945 | ||
| chr8:100062748
|
G | A | 1 | a0014 | 1 | NA18991.hp1 | missense_variant | MODERATE | c.1357C>T | p.Leu453Phe | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/28 | 1485/4229 | 1357/3795 | 453/1264 | chr8 | 100062748 | ||
| chr8:100062750
|
T | A | 1 | a0014 | 1 | NA18991.hp1 | missense_variant&splice_region_variant | MODERATE | c.1355A>T | p.His452Leu | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/28 | 1483/4229 | 1355/3795 | 452/1264 | chr8 | 100062750 | ||
| chr8:100062751
|
G | T | 1 | a0014 | 1 | NA18991.hp1 | missense_variant&splice_region_variant | MODERATE | c.1354C>A | p.His452Asn | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/28 | 1482/4229 | 1354/3795 | 452/1264 | chr8 | 100062751 | ||
| chr8:100063480
|
A | C | 1 | a0010 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.1288T>G | p.Tyr430Asp | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 8/28 | 1416/4229 | 1288/3795 | 430/1264 | chr8 | 100063480 | ||
| chr8:100063578
|
C | A | 1 | a0004 | 3 | NA18970.hp1 NA19068.hp1 NA19087.hp1 |
missense_variant | MODERATE | c.1190G>T | p.Arg397Met | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 8/28 | 1318/4229 | 1190/3795 | 397/1264 | chr8 | 100063578 | ||
| chr8:100063702
|
A | G | 1 | a0015 | 1 | NA19058.hp1 | missense_variant | MODERATE | c.1066T>C | p.Cys356Arg | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 8/28 | 1194/4229 | 1066/3795 | 356/1264 | chr8 | 100063702 | ||
| chr8:100063946
|
T | G | 3 | a0003a0008a0012 | 17 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(14): Show |
missense_variant | MODERATE | c.822A>C | p.Glu274Asp | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 8/28 | 950/4229 | 822/3795 | 274/1264 | chr8 | 100063946 | ||
| chr8:100063982
|
G | T | 2 | a0010a0011 | 2 | HG03225.hp2 HG03540.hp1 |
missense_variant | MODERATE | c.786C>A | p.Asn262Lys | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 8/28 | 914/4229 | 786/3795 | 262/1264 | chr8 | 100063982 | ||
| chr8:100066172
|
A | G | 1 | a0009 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.719T>C | p.Val240Ala | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 7/28 | 847/4229 | 719/3795 | 240/1264 | chr8 | 100066172 | ||
| chr8:100071455
|
C | T | 1 | a0008 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.508G>A | p.Val170Met | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/28 | 636/4229 | 508/3795 | 170/1264 | chr8 | 100071455 | ||
| chr8:100105912
|
T | G | 1 | a0016 | 1 | NA18963.hp1 | missense_variant | MODERATE | c.10A>C | p.Lys4Gln | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 1/28 | 138/4229 | 10/3795 | 4/1264 | chr8 | 100105912 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:99962943
|
T | C | 2 | a0001c0004a0003c0022 | 16 | HG00733.hp1 HG00738.hp2 HG01243.hp1 others(13): Show |
synonymous_variant | LOW | c.3651A>G | p.Leu1217Leu | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 25/28 | 3779/4229 | 3651/3795 | 1217/1264 | chr8 | 99962943 | ||
| chr8:99977949
|
A | G | 4 | a0001c0003a0002c0011a0015c0017others(1): Show | 24 | HG02145.hp1 HG02257.hp2 HG02280.hp2 others(21): Show |
synonymous_variant | LOW | c.3487T>C | p.Leu1163Leu | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/28 | 3615/4229 | 3487/3795 | 1163/1264 | chr8 | 99977949 | ||
| chr8:100008519
|
G | A | 1 | a0001c0012 | 2 | HG02145.hp2 HG03209.hp1 |
synonymous_variant | LOW | c.2217C>T | p.Leu739Leu | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 15/28 | 2345/4229 | 2217/3795 | 739/1264 | chr8 | 100008519 | ||
| chr8:100093501
|
A | G | 1 | a0001c0009 | 2 | HG02486.hp2 HG02572.hp2 |
synonymous_variant | LOW | c.63T>C | p.Ser21Ser | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/28 | 191/4229 | 63/3795 | 21/1264 | chr8 | 100093501 | ||
| chr8:100105386
|
T | C | 1 | a0001c0024 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.42A>G | p.Thr14Thr | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/28 | 170/4229 | 42/3795 | 14/1264 | chr8 | 100105386 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:99960966
|
T | C | 1 | a0001c0001t0004 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*276A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 28/28 | 1473 | chr8 | 99960966 | |||||
| chr8:99961022
|
T | C | 2 | a0001c0001t0003a0012c0023t0003 | 2 | HG01243.hp2 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*220A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 28/28 | 1417 | chr8 | 99961022 | |||||
| chr8:99961070
|
A | C | 3 | a0001c0004t0002a0001c0004t0005a0003c0022t0002 | 16 | HG00733.hp1 HG00738.hp2 HG01243.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*172T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 28/28 | 1369 | chr8 | 99961070 | |||||
| chr8:100105980
|
G | C | 1 | a0001c0004t0005 | 1 | HG02809.hp2 | 5_prime_UTR_variant | MODIFIER | c.-59C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 1/28 | 59 | chr8 | 100105980 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:99961237
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.*46-41A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 27/27 | chr8 | 99961237 | ||||||
| chr8:99961321
|
A | C | 16 | a0001c0004t0002g0053a0001c0004t0002g0054a0001c0004t0002g0062others(13): Show | 16 | HG00733.hp1 HG00738.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.*46-125T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 27/27 | chr8 | 99961321 | ||||||
| chr8:99961388
|
G | T | 38 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(35): Show | 39 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.*46-192C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 27/27 | chr8 | 99961388 | ||||||
| chr8:99961531
|
C | T | 34 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(31): Show | 35 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.*46-335G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 27/27 | chr8 | 99961531 | ||||||
| chr8:99961791
|
T | C | 1 | a0001c0009t0001g0100 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.*46-595A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 27/27 | chr8 | 99961791 | ||||||
| chr8:99962014
|
T | A | 1 | a0001c0001t0001g0104 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.*45+380A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 27/27 | chr8 | 99962014 | ||||||
| chr8:99962065
|
CT | C | 304 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0006others(301): Show | 306 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.*45+328delA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 27/27 | chr8 | 99962065 | ||||||
| chr8:99962131
|
C | G | 1 | a0001c0001t0001g0201 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.*45+263G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 27/27 | chr8 | 99962131 | ||||||
| chr8:99962275
|
C | T | 38 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(35): Show | 39 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.*45+119G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 27/27 | chr8 | 99962275 | ||||||
| chr8:99962774
|
A | G | 304 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(301): Show | 306 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(303): Show |
splice_region_variant&intron_variant | LOW | c.3710-7T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 25/27 | chr8 | 99962774 | ||||||
| chr8:99962779
|
TAAAAG | T | 3 | a0006c0007t0001g0113a0006c0007t0001g0125a0006c0007t0001g0126 | 3 | HG01884.hp2 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3710-17_3710-13del others(5): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 25/27 | chr8 | 99962779 | ||||||
| chr8:99963130
|
T | C | 2 | a0001c0003t0001g0140a0001c0003t0001g0214 | 2 | NA18962.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.3616-152A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 24/27 | chr8 | 99963130 | ||||||
| chr8:99963195
|
C | A | 14 | a0001c0001t0001g0093a0001c0001t0001g0270a0001c0001t0001g0272others(11): Show | 14 | HG00408.hp2 HG00558.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.3616-217G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 24/27 | chr8 | 99963195 | ||||||
| chr8:99963722
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3616-744G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 24/27 | chr8 | 99963722 | ||||||
| chr8:99963824
|
G | C | 1 | a0001c0004t0002g0121 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3616-846C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 24/27 | chr8 | 99963824 | ||||||
| chr8:99963829
|
A | C | 3 | a0006c0007t0001g0113a0006c0007t0001g0125a0006c0007t0001g0126 | 3 | HG01884.hp2 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3616-851T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 24/27 | chr8 | 99963829 | ||||||
| chr8:99964069
|
TTC | T | 67 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0037others(64): Show | 68 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.3616-1093_3616-109 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 24/27 | chr8 | 99964069 | ||||||
| chr8:99964274
|
G | A | 3 | a0001c0001t0001g0067a0001c0001t0001g0128a0001c0001t0001g0199 | 3 | HG03041.hp1 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3615+1061C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 24/27 | chr8 | 99964274 | ||||||
| chr8:99964326
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.3615+1009G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 24/27 | chr8 | 99964326 | ||||||
| chr8:99964439
|
G | C | 44 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(41): Show | 45 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.3615+896C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 24/27 | chr8 | 99964439 | ||||||
| chr8:99964477
|
C | CA | 27 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0041others(24): Show | 28 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.3615+857dupT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 24/27 | chr8 | 99964477 | ||||||
| chr8:99964477
|
C | CAA | 7 | a0001c0001t0001g0118a0001c0001t0001g0136a0001c0001t0001g0205others(4): Show | 7 | HG02145.hp2 HG02922.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.3615+856_3615+857d others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 24/27 | chr8 | 99964477 | ||||||
| chr8:99964477
|
CA | C | 9 | a0001c0001t0001g0013a0001c0001t0001g0099a0001c0001t0001g0141others(6): Show | 9 | HG02572.hp1 HG02735.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.3615+857delT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 24/27 | chr8 | 99964477 | ||||||
| chr8:99964489
|
A | C | 1 | a0002c0002t0001g0087 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.3615+846T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 24/27 | chr8 | 99964489 | ||||||
| chr8:99964600
|
G | T | 1 | a0001c0001t0001g0296 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3615+735C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 24/27 | chr8 | 99964600 | ||||||
| chr8:99964992
|
G | C | 1 | a0001c0001t0001g0295 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3615+343C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 24/27 | chr8 | 99964992 | ||||||
| chr8:99965309
|
A | T | 4 | a0001c0001t0001g0118a0001c0001t0001g0253a0001c0012t0001g0112others(1): Show | 4 | HG02145.hp2 HG02922.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.3615+26T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 24/27 | chr8 | 99965309 | ||||||
| chr8:99965576
|
T | C | 1 | a0003c0005t0001g0059 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3520-146A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99965576 | ||||||
| chr8:99965673
|
A | G | 3 | a0006c0007t0001g0113a0006c0007t0001g0125a0006c0007t0001g0126 | 3 | HG01884.hp2 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3520-243T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99965673 | ||||||
| chr8:99965815
|
C | G | 36 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(33): Show | 37 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.3520-385G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99965815 | ||||||
| chr8:99965951
|
C | T | 1 | a0003c0005t0001g0059 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3520-521G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99965951 | ||||||
| chr8:99965997
|
A | C | 1 | a0001c0001t0001g0104 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3520-567T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99965997 | ||||||
| chr8:99966241
|
T | C | 1 | a0001c0001t0001g0240 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3520-811A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99966241 | ||||||
| chr8:99966272
|
A | G | 1 | a0001c0001t0003g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3520-842T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99966272 | ||||||
| chr8:99966377
|
C | T | 34 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(31): Show | 35 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.3520-947G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99966377 | ||||||
| chr8:99966405
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3520-975G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99966405 | ||||||
| chr8:99966429
|
T | G | 1 | a0001c0001t0001g0090 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3520-999A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99966429 | ||||||
| chr8:99966459
|
GA | G | 38 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(35): Show | 39 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.3520-1030delT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99966459 | ||||||
| chr8:99966851
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3520-1421A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99966851 | ||||||
| chr8:99966856
|
G | A | 1 | a0016c0025t0001g0307 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3520-1426C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99966856 | ||||||
| chr8:99966902
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3520-1472A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99966902 | ||||||
| chr8:99967023
|
C | G | 3 | a0001c0001t0001g0240a0002c0002t0001g0213a0005c0006t0001g0091 | 3 | NA18979.hp1 NA19074.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.3520-1593G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99967023 | ||||||
| chr8:99967123
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3520-1693G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99967123 | ||||||
| chr8:99967206
|
C | T | 224 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(221): Show | 226 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(223): Show |
intron_variant | MODIFIER | c.3520-1776G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99967206 | ||||||
| chr8:99967231
|
G | A | 3 | a0006c0007t0001g0113a0006c0007t0001g0125a0006c0007t0001g0126 | 3 | HG01884.hp2 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3520-1801C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99967231 | ||||||
| chr8:99967336
|
T | TG | 3 | a0006c0007t0001g0113a0006c0007t0001g0125a0006c0007t0001g0126 | 3 | HG01884.hp2 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3520-1907_3520-190 others(5): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99967336 | ||||||
| chr8:99967350
|
C | T | 1 | a0000c0019t0001g0248 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3520-1920G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99967350 | ||||||
| chr8:99967415
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3520-1985T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99967415 | ||||||
| chr8:99967648
|
C | G | 1 | a0001c0001t0001g0200 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.3520-2218G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99967648 | ||||||
| chr8:99967670
|
C | A | 1 | a0001c0001t0001g0183 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3520-2240G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99967670 | ||||||
| chr8:99967713
|
A | T | 36 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(33): Show | 37 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.3520-2283T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99967713 | ||||||
| chr8:99967761
|
C | T | 1 | a0007c0010t0001g0171 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.3520-2331G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99967761 | ||||||
| chr8:99967801
|
G | A | 6 | a0001c0001t0001g0037a0001c0001t0001g0226a0001c0003t0001g0140others(3): Show | 6 | HG03471.hp2 NA18962.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.3520-2371C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99967801 | ||||||
| chr8:99967874
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3520-2444C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99967874 | ||||||
| chr8:99967959
|
G | A | 7 | a0001c0001t0001g0139a0001c0001t0001g0143a0001c0001t0001g0175others(4): Show | 7 | HG00438.hp1 HG00621.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.3520-2529C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99967959 | ||||||
| chr8:99968265
|
A | C | 6 | a0001c0001t0001g0066a0001c0001t0001g0111a0001c0001t0001g0233others(3): Show | 6 | HG02280.hp1 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.3520-2835T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99968265 | ||||||
| chr8:99968387
|
C | T | 1 | a0002c0011t0001g0071 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3520-2957G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99968387 | ||||||
| chr8:99968533
|
C | T | 5 | a0001c0001t0001g0144a0001c0001t0001g0165a0001c0001t0001g0167others(2): Show | 6 | HG02486.hp1 HG03139.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.3520-3103G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99968533 | ||||||
| chr8:99968599
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3520-3169A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99968599 | ||||||
| chr8:99968840
|
G | A | 3 | a0001c0001t0001g0253a0001c0012t0001g0112a0003c0005t0001g0061 | 3 | HG02145.hp2 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3520-3410C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99968840 | ||||||
| chr8:99968861
|
G | A | 38 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(35): Show | 39 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.3520-3431C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99968861 | ||||||
| chr8:99968978
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.3520-3548C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99968978 | ||||||
| chr8:99969069
|
A | G | 1 | a0001c0001t0001g0188 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3520-3639T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99969069 | ||||||
| chr8:99969296
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3520-3866A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99969296 | ||||||
| chr8:99969424
|
A | G | 42 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(39): Show | 43 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.3520-3994T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99969424 | ||||||
| chr8:99969472
|
G | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0219 | 2 | HG01123.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.3520-4042C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99969472 | ||||||
| chr8:99969528
|
G | T | 1 | a0012c0023t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3520-4098C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99969528 | ||||||
| chr8:99969593
|
G | A | 38 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(35): Show | 39 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.3520-4163C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99969593 | ||||||
| chr8:99969597
|
CAG | C | 34 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(31): Show | 35 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.3520-4169_3520-416 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99969597 | ||||||
| chr8:99969981
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3520-4551T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99969981 | ||||||
| chr8:99970016
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3520-4586T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99970016 | ||||||
| chr8:99970179
|
A | C | 1 | a0001c0001t0001g0004 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3520-4749T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99970179 | ||||||
| chr8:99970298
|
T | C | 2 | a0001c0001t0003g0003a0012c0023t0003g0105 | 2 | HG01243.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.3520-4868A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99970298 | ||||||
| chr8:99970478
|
C | T | 1 | a0002c0002t0001g0289 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3520-5048G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99970478 | ||||||
| chr8:99970510
|
G | T | 1 | a0001c0001t0003g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3520-5080C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99970510 | ||||||
| chr8:99970605
|
A | G | 36 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(33): Show | 37 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.3520-5175T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99970605 | ||||||
| chr8:99971024
|
C | T | 1 | a0002c0002t0001g0289 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3520-5594G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99971024 | ||||||
| chr8:99971304
|
T | A | 2 | a0001c0001t0003g0003a0012c0023t0003g0105 | 2 | HG01243.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.3520-5874A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99971304 | ||||||
| chr8:99971340
|
C | A | 1 | a0002c0002t0001g0259 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3520-5910G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99971340 | ||||||
| chr8:99971423
|
G | C | 2 | a0001c0001t0001g0282a0001c0001t0001g0285 | 2 | HG02027.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.3520-5993C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99971423 | ||||||
| chr8:99971453
|
G | C | 4 | a0001c0001t0001g0139a0001c0001t0001g0143a0001c0001t0001g0175others(1): Show | 4 | HG00438.hp1 HG00621.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.3520-6023C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99971453 | ||||||
| chr8:99971559
|
C | A | 39 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(36): Show | 40 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.3520-6129G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99971559 | ||||||
| chr8:99971585
|
GACAA | G | 3 | a0006c0007t0001g0113a0006c0007t0001g0125a0006c0007t0001g0126 | 3 | HG01884.hp2 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3520-6159_3520-615 others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99971585 | ||||||
| chr8:99971821
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3519+6096A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99971821 | ||||||
| chr8:99971868
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3519+6049A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99971868 | ||||||
| chr8:99971911
|
T | C | 16 | a0001c0004t0002g0053a0001c0004t0002g0054a0001c0004t0002g0062others(13): Show | 16 | HG00733.hp1 HG00738.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.3519+6006A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99971911 | ||||||
| chr8:99972670
|
A | G | 1 | a0004c0008t0001g0173 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3519+5247T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99972670 | ||||||
| chr8:99972743
|
C | T | 2 | a0001c0001t0001g0182a0001c0001t0001g0290 | 2 | HG01175.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.3519+5174G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99972743 | ||||||
| chr8:99972917
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3519+5000G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99972917 | ||||||
| chr8:99972983
|
C | CA | 66 | a0001c0001t0001g0030a0001c0001t0001g0037a0001c0001t0001g0041others(63): Show | 67 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.3519+4933dupT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99972983 | ||||||
| chr8:99973015
|
T | C | 45 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(42): Show | 46 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.3519+4902A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99973015 | ||||||
| chr8:99973065
|
G | A | 16 | a0001c0004t0002g0053a0001c0004t0002g0054a0001c0004t0002g0062others(13): Show | 16 | HG00733.hp1 HG00738.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.3519+4852C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99973065 | ||||||
| chr8:99973104
|
G | A | 1 | a0003c0022t0002g0110 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3519+4813C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99973104 | ||||||
| chr8:99973171
|
C | T | 1 | a0001c0001t0003g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3519+4746G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99973171 | ||||||
| chr8:99973537
|
G | C | 36 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(33): Show | 37 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.3519+4380C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99973537 | ||||||
| chr8:99973563
|
T | C | 2 | a0007c0010t0001g0171a0007c0010t0001g0291 | 2 | NA18968.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.3519+4354A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99973563 | ||||||
| chr8:99973586
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3519+4331G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99973586 | ||||||
| chr8:99973738
|
G | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0003g0003others(4): Show | 7 | HG01243.hp2 HG02818.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.3519+4179C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99973738 | ||||||
| chr8:99973756
|
C | T | 3 | a0006c0007t0001g0113a0006c0007t0001g0125a0006c0007t0001g0126 | 3 | HG01884.hp2 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3519+4161G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99973756 | ||||||
| chr8:99973868
|
C | CA | 44 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0041others(41): Show | 45 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.3519+4048dupT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99973868 | ||||||
| chr8:99973883
|
C | A | 1 | a0001c0001t0001g0047 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3519+4034G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99973883 | ||||||
| chr8:99973996
|
A | C | 3 | a0006c0007t0001g0113a0006c0007t0001g0125a0006c0007t0001g0126 | 3 | HG01884.hp2 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3519+3921T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99973996 | ||||||
| chr8:99974493
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3519+3424T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99974493 | ||||||
| chr8:99974499
|
A | T | 14 | a0001c0001t0001g0093a0001c0001t0001g0270a0001c0001t0001g0272others(11): Show | 14 | HG00408.hp2 HG00558.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.3519+3418T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99974499 | ||||||
| chr8:99974595
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0028 | 2 | HG02300.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.3519+3322G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99974595 | ||||||
| chr8:99974795
|
C | CA | 57 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0035others(54): Show | 58 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.3519+3121dupT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99974795 | ||||||
| chr8:99974827
|
A | G | 4 | a0001c0001t0001g0012a0001c0001t0001g0231a0001c0001t0001g0260others(1): Show | 4 | HG00544.hp2 NA18973.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.3519+3090T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99974827 | ||||||
| chr8:99974949
|
A | G | 3 | a0006c0007t0001g0113a0006c0007t0001g0125a0006c0007t0001g0126 | 3 | HG01884.hp2 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3519+2968T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99974949 | ||||||
| chr8:99974954
|
T | C | 35 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(32): Show | 36 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.3519+2963A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99974954 | ||||||
| chr8:99975020
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3519+2897G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99975020 | ||||||
| chr8:99975065
|
G | C | 1 | a0001c0001t0001g0004 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3519+2852C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99975065 | ||||||
| chr8:99975233
|
A | C | 3 | a0006c0007t0001g0113a0006c0007t0001g0125a0006c0007t0001g0126 | 3 | HG01884.hp2 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3519+2684T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99975233 | ||||||
| chr8:99975284
|
A | G | 1 | a0001c0001t0003g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3519+2633T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99975284 | ||||||
| chr8:99975437
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3519+2480G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99975437 | ||||||
| chr8:99975604
|
C | CA | 34 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(31): Show | 35 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.3519+2312dupT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99975604 | ||||||
| chr8:99975838
|
T | A | 66 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0037others(63): Show | 67 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.3519+2079A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99975838 | ||||||
| chr8:99975947
|
T | C | 1 | a0001c0001t0001g0243 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3519+1970A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99975947 | ||||||
| chr8:99975988
|
G | A | 3 | a0001c0001t0001g0024a0005c0006t0001g0082a0005c0006t0001g0092 | 3 | HG01081.hp1 NA18966.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.3519+1929C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99975988 | ||||||
| chr8:99975990
|
G | A | 3 | a0006c0007t0001g0113a0006c0007t0001g0125a0006c0007t0001g0126 | 3 | HG01884.hp2 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3519+1927C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99975990 | ||||||
| chr8:99976051
|
A | G | 3 | a0006c0007t0001g0113a0006c0007t0001g0125a0006c0007t0001g0126 | 3 | HG01884.hp2 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3519+1866T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99976051 | ||||||
| chr8:99976147
|
A | G | 38 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(35): Show | 39 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.3519+1770T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99976147 | ||||||
| chr8:99976161
|
G | C | 4 | a0001c0001t0001g0139a0001c0001t0001g0143a0001c0001t0001g0175others(1): Show | 4 | HG00438.hp1 HG00621.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.3519+1756C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99976161 | ||||||
| chr8:99976206
|
A | T | 1 | a0001c0001t0003g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3519+1711T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99976206 | ||||||
| chr8:99976301
|
C | A | 40 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(37): Show | 41 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.3519+1616G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99976301 | ||||||
| chr8:99976350
|
T | TTTTG | 3 | a0006c0007t0001g0113a0006c0007t0001g0125a0006c0007t0001g0126 | 3 | HG01884.hp2 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3519+1563_3519+156 others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99976350 | ||||||
| chr8:99976423
|
G | A | 5 | a0002c0002t0001g0058a0002c0002t0001g0081a0002c0002t0001g0083others(2): Show | 5 | NA18944.hp2 NA18949.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.3519+1494C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99976423 | ||||||
| chr8:99976510
|
T | C | 5 | a0002c0002t0001g0058a0002c0002t0001g0081a0002c0002t0001g0083others(2): Show | 5 | NA18944.hp2 NA18949.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.3519+1407A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99976510 | ||||||
| chr8:99976516
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3519+1401G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99976516 | ||||||
| chr8:99976523
|
G | A | 3 | a0001c0001t0001g0232a0001c0001t0001g0235a0001c0001t0001g0262 | 3 | NA18963.hp2 NA18965.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.3519+1394C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99976523 | ||||||
| chr8:99976567
|
T | C | 4 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0026others(1): Show | 4 | NA18952.hp1 NA19068.hp2 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.3519+1350A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99976567 | ||||||
| chr8:99976578
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3519+1339C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99976578 | ||||||
| chr8:99976607
|
C | T | 2 | a0001c0001t0001g0182a0001c0001t0001g0290 | 2 | HG01175.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.3519+1310G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99976607 | ||||||
| chr8:99976650
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3519+1267A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99976650 | ||||||
| chr8:99976667
|
C | T | 9 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(6): Show | 9 | HG00621.hp1 HG00735.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.3519+1250G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99976667 | ||||||
| chr8:99976716
|
C | G | 1 | a0001c0001t0001g0265 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3519+1201G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99976716 | ||||||
| chr8:99976861
|
T | C | 1 | a0002c0002t0001g0058 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3519+1056A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99976861 | ||||||
| chr8:99976943
|
G | T | 1 | a0003c0005t0001g0060 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3519+974C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99976943 | ||||||
| chr8:99976961
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.3519+956C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99976961 | ||||||
| chr8:99977156
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.3519+761A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99977156 | ||||||
| chr8:99977157
|
G | GT | 16 | a0001c0004t0002g0053a0001c0004t0002g0054a0001c0004t0002g0062others(13): Show | 16 | HG00733.hp1 HG00738.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.3519+759dupA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99977157 | ||||||
| chr8:99977270
|
A | AT | 25 | a0001c0001t0001g0042a0001c0001t0001g0103a0001c0001t0001g0139others(22): Show | 25 | HG00438.hp1 HG00738.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.3519+646dupA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99977270 | ||||||
| chr8:99977270
|
AT | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0163others(3): Show | 6 | HG01168.hp1 HG02735.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.3519+646delA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99977270 | ||||||
| chr8:99977270
|
ATTTTT | A | 30 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(27): Show | 31 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.3519+642_3519+646d others(7): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99977270 | ||||||
| chr8:99977311
|
T | C | 42 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(39): Show | 43 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.3519+606A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99977311 | ||||||
| chr8:99977603
|
T | C | 1 | a0001c0001t0001g0104 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3519+314A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99977603 | ||||||
| chr8:99977663
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3519+254G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99977663 | ||||||
| chr8:99977727
|
A | C | 1 | a0002c0011t0001g0071 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3519+190T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99977727 | ||||||
| chr8:99977819
|
C | A | 1 | a0001c0001t0001g0044 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3519+98G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 23/27 | chr8 | 99977819 | ||||||
| chr8:99978091
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3361-16A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99978091 | ||||||
| chr8:99978272
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.3361-197A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99978272 | ||||||
| chr8:99978278
|
T | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0028 | 2 | HG02300.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.3361-203A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99978278 | ||||||
| chr8:99978645
|
C | T | 1 | a0001c0009t0001g0101 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3361-570G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99978645 | ||||||
| chr8:99978790
|
T | G | 38 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(35): Show | 39 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.3361-715A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99978790 | ||||||
| chr8:99979139
|
T | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0028 | 2 | HG02300.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.3361-1064A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99979139 | ||||||
| chr8:99979141
|
C | T | 3 | a0006c0007t0001g0113a0006c0007t0001g0125a0006c0007t0001g0126 | 3 | HG01884.hp2 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3361-1066G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99979141 | ||||||
| chr8:99979258
|
A | G | 3 | a0006c0007t0001g0113a0006c0007t0001g0125a0006c0007t0001g0126 | 3 | HG01884.hp2 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3361-1183T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99979258 | ||||||
| chr8:99979381
|
T | C | 16 | a0001c0004t0002g0053a0001c0004t0002g0054a0001c0004t0002g0062others(13): Show | 16 | HG00733.hp1 HG00738.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.3361-1306A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99979381 | ||||||
| chr8:99979427
|
C | T | 2 | a0001c0003t0001g0140a0001c0003t0001g0214 | 2 | NA18962.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.3361-1352G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99979427 | ||||||
| chr8:99979448
|
A | G | 1 | a0001c0001t0001g0252 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3361-1373T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99979448 | ||||||
| chr8:99979528
|
T | C | 1 | a0001c0001t0001g0026 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.3361-1453A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99979528 | ||||||
| chr8:99979570
|
A | C | 4 | a0001c0001t0001g0118a0001c0001t0001g0253a0001c0012t0001g0112others(1): Show | 4 | HG02145.hp2 HG02922.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.3361-1495T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99979570 | ||||||
| chr8:99979851
|
G | C | 34 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(31): Show | 35 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.3361-1776C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99979851 | ||||||
| chr8:99979981
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.3361-1906T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99979981 | ||||||
| chr8:99980005
|
A | C | 1 | a0001c0003t0001g0080 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3361-1930T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99980005 | ||||||
| chr8:99980231
|
A | G | 294 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(291): Show | 296 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(293): Show |
intron_variant | MODIFIER | c.3360+1706T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99980231 | ||||||
| chr8:99980375
|
A | T | 1 | a0001c0001t0001g0220 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3360+1562T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99980375 | ||||||
| chr8:99980609
|
A | C | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3360+1328T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99980609 | ||||||
| chr8:99980692
|
T | G | 1 | a0001c0004t0002g0114 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3360+1245A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99980692 | ||||||
| chr8:99980784
|
C | T | 2 | a0001c0001t0001g0186a0001c0001t0001g0286 | 2 | HG02083.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.3360+1153G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99980784 | ||||||
| chr8:99980785
|
G | A | 34 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(31): Show | 35 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.3360+1152C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99980785 | ||||||
| chr8:99980919
|
C | T | 30 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0003g0003others(27): Show | 31 | HG01243.hp2 HG02145.hp1 HG02257.hp2 others(28): Show |
intron_variant | MODIFIER | c.3360+1018G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99980919 | ||||||
| chr8:99981007
|
C | T | 2 | a0001c0009t0001g0100a0001c0009t0001g0101 | 2 | HG02486.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.3360+930G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99981007 | ||||||
| chr8:99981244
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3360+693C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99981244 | ||||||
| chr8:99981265
|
G | T | 3 | a0001c0001t0001g0067a0001c0001t0001g0128a0001c0001t0001g0199 | 3 | HG03041.hp1 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3360+672C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99981265 | ||||||
| chr8:99981322
|
T | C | 89 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0037others(86): Show | 91 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.3360+615A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99981322 | ||||||
| chr8:99981435
|
C | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0041 | 2 | HG00099.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.3360+502G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99981435 | ||||||
| chr8:99981435
|
C | G | 41 | a0001c0001t0001g0051a0001c0001t0001g0093a0001c0001t0001g0103others(38): Show | 42 | HG00408.hp2 HG00558.hp2 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.3360+502G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99981435 | ||||||
| chr8:99981520
|
T | C | 33 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(30): Show | 34 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.3360+417A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99981520 | ||||||
| chr8:99981525
|
T | C | 16 | a0001c0004t0002g0053a0001c0004t0002g0054a0001c0004t0002g0062others(13): Show | 16 | HG00733.hp1 HG00738.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.3360+412A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99981525 | ||||||
| chr8:99981724
|
G | GT | 8 | a0001c0001t0001g0118a0001c0001t0001g0204a0001c0001t0001g0224others(5): Show | 8 | HG01099.hp2 HG02145.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.3360+212dupA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99981724 | ||||||
| chr8:99981724
|
GT | G | 60 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0037others(57): Show | 61 | HG00733.hp1 HG00738.hp2 HG01168.hp1 others(58): Show |
intron_variant | MODIFIER | c.3360+212delA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99981724 | ||||||
| chr8:99981840
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3360+97C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99981840 | ||||||
| chr8:99981898
|
A | G | 43 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(40): Show | 44 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.3360+39T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 22/27 | chr8 | 99981898 | ||||||
| chr8:99982134
|
T | C | 9 | a0001c0003t0001g0078a0001c0003t0001g0079a0001c0003t0001g0080others(6): Show | 9 | NA18612.hp2 NA18747.hp1 NA18950.hp2 others(6): Show |
intron_variant | MODIFIER | c.3181-18A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99982134 | ||||||
| chr8:99982161
|
C | T | 120 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(117): Show | 122 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.3181-45G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99982161 | ||||||
| chr8:99982483
|
C | G | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3181-367G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99982483 | ||||||
| chr8:99982800
|
A | T | 1 | a0001c0001t0001g0015 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.3181-684T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99982800 | ||||||
| chr8:99982844
|
C | T | 16 | a0001c0004t0002g0053a0001c0004t0002g0054a0001c0004t0002g0062others(13): Show | 16 | HG00733.hp1 HG00738.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.3181-728G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99982844 | ||||||
| chr8:99982919
|
C | T | 32 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(29): Show | 33 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.3181-803G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99982919 | ||||||
| chr8:99983011
|
T | C | 3 | a0006c0007t0001g0113a0006c0007t0001g0125a0006c0007t0001g0126 | 3 | HG01884.hp2 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3181-895A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99983011 | ||||||
| chr8:99983056
|
A | T | 43 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(40): Show | 44 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.3181-940T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99983056 | ||||||
| chr8:99983485
|
A | C | 39 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(36): Show | 40 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.3181-1369T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99983485 | ||||||
| chr8:99983502
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3181-1386A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99983502 | ||||||
| chr8:99983667
|
T | A | 2 | a0001c0001t0001g0205a0001c0001t0001g0212 | 2 | HG00597.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.3181-1551A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99983667 | ||||||
| chr8:99983927
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3181-1811G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99983927 | ||||||
| chr8:99983968
|
C | G | 2 | a0001c0001t0001g0270a0001c0001t0001g0272 | 2 | HG00408.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.3181-1852G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99983968 | ||||||
| chr8:99984219
|
T | C | 43 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(40): Show | 44 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.3181-2103A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99984219 | ||||||
| chr8:99984437
|
A | AT | 44 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0051others(41): Show | 45 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.3181-2322dupA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99984437 | ||||||
| chr8:99984437
|
AT | A | 54 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0102others(51): Show | 55 | HG00733.hp1 HG00738.hp2 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.3181-2322delA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99984437 | ||||||
| chr8:99984562
|
G | C | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3181-2446C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99984562 | ||||||
| chr8:99984674
|
T | G | 43 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0030others(40): Show | 44 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.3181-2558A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99984674 | ||||||
| chr8:99984774
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3181-2658A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99984774 | ||||||
| chr8:99984786
|
C | T | 50 | a0001c0001t0001g0037a0001c0001t0001g0104a0001c0001t0001g0118others(47): Show | 51 | HG00733.hp1 HG00738.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.3181-2670G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99984786 | ||||||
| chr8:99984788
|
G | GAC | 61 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(58): Show | 62 | HG01071.hp2 HG01168.hp1 HG01175.hp2 others(59): Show |
intron_variant | MODIFIER | c.3180+2668_3180+266 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99984788 | ||||||
| chr8:99984788
|
G | GACAC | 28 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0027others(25): Show | 29 | HG00733.hp1 HG00738.hp2 HG02486.hp1 others(26): Show |
intron_variant | MODIFIER | c.3180+2666_3180+266 others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99984788 | ||||||
| chr8:99984788
|
G | GACACAC | 21 | a0001c0001t0001g0017a0001c0001t0001g0041a0001c0001t0001g0093others(18): Show | 21 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.3180+2664_3180+266 others(10): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99984788 | ||||||
| chr8:99984788
|
G | GACACACA others(1): Show |
3 | a0001c0001t0001g0023a0001c0001t0003g0003a0002c0002t0001g0133 | 3 | HG01243.hp2 HG04184.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.3180+2662_3180+266 others(12): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99984788 | ||||||
| chr8:99984788
|
G | GACACACA others(3): Show |
2 | a0003c0005t0001g0068a0003c0005t0001g0094 | 2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3180+2660_3180+266 others(14): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99984788 | ||||||
| chr8:99984788
|
GAC | G | 3 | a0001c0001t0001g0103a0001c0003t0001g0079a0012c0023t0003g0105 | 3 | HG02630.hp1 HG02818.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.3180+2668_3180+266 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99984788 | ||||||
| chr8:99984788
|
GACACAC | G | 4 | a0001c0001t0001g0012a0001c0001t0001g0231a0001c0001t0001g0260others(1): Show | 4 | HG00544.hp2 NA18973.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.3180+2664_3180+266 others(10): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99984788 | ||||||
| chr8:99984927
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3180+2531G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99984927 | ||||||
| chr8:99985193
|
C | T | 5 | a0001c0001t0001g0103a0001c0001t0001g0253a0001c0004t0002g0120others(2): Show | 5 | HG01243.hp1 HG02630.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.3180+2265G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99985193 | ||||||
| chr8:99985338
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3180+2120T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99985338 | ||||||
| chr8:99985393
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3180+2065G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99985393 | ||||||
| chr8:99985408
|
C | T | 22 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0042others(19): Show | 23 | HG00408.hp2 HG02040.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.3180+2050G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99985408 | ||||||
| chr8:99985460
|
A | G | 1 | a0001c0001t0001g0301 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3180+1998T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99985460 | ||||||
| chr8:99985461
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3180+1997A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99985461 | ||||||
| chr8:99985486
|
C | T | 61 | a0000c0019t0001g0248a0001c0001t0001g0006a0001c0001t0001g0007others(58): Show | 61 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.3180+1972G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99985486 | ||||||
| chr8:99985511
|
C | G | 114 | a0000c0019t0001g0248a0001c0001t0001g0006a0001c0001t0001g0007others(111): Show | 116 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.3180+1947G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99985511 | ||||||
| chr8:99985598
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3180+1860G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99985598 | ||||||
| chr8:99985989
|
ATGTGAAA others(3): Show |
A | 1 | a0001c0001t0001g0228 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3180+1459_3180+146 others(14): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99985989 | ||||||
| chr8:99986018
|
A | C | 2 | a0001c0009t0001g0100a0001c0009t0001g0101 | 2 | HG02486.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.3180+1440T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99986018 | ||||||
| chr8:99986245
|
T | C | 4 | a0001c0001t0001g0067a0001c0001t0001g0098a0001c0001t0001g0128others(1): Show | 4 | HG01099.hp1 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.3180+1213A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99986245 | ||||||
| chr8:99986260
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3180+1198A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99986260 | ||||||
| chr8:99986321
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3180+1137T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99986321 | ||||||
| chr8:99986430
|
G | T | 15 | a0001c0001t0001g0298a0003c0005t0001g0002a0003c0005t0001g0057others(12): Show | 16 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.3180+1028C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99986430 | ||||||
| chr8:99986431
|
C | T | 15 | a0001c0001t0001g0298a0003c0005t0001g0002a0003c0005t0001g0057others(12): Show | 16 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.3180+1027G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99986431 | ||||||
| chr8:99986515
|
G | A | 18 | a0001c0001t0001g0118a0001c0001t0001g0129a0001c0001t0001g0284others(15): Show | 18 | HG00733.hp1 HG00738.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.3180+943C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99986515 | ||||||
| chr8:99986533
|
T | C | 7 | a0001c0001t0001g0103a0001c0001t0001g0104a0003c0005t0001g0106others(4): Show | 7 | HG01884.hp2 HG02630.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.3180+925A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99986533 | ||||||
| chr8:99986654
|
C | T | 5 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0024others(2): Show | 5 | NA18952.hp1 NA19063.hp2 NA19068.hp2 others(2): Show |
intron_variant | MODIFIER | c.3180+804G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99986654 | ||||||
| chr8:99986669
|
T | C | 1 | a0015c0017t0001g0046 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3180+789A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99986669 | ||||||
| chr8:99987082
|
G | A | 1 | a0012c0023t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3180+376C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99987082 | ||||||
| chr8:99987347
|
A | T | 80 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(77): Show | 80 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.3180+111T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99987347 | ||||||
| chr8:99987388
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.3180+70A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99987388 | ||||||
| chr8:99987409
|
G | A | 46 | a0000c0019t0001g0248a0001c0001t0001g0008a0001c0001t0001g0018others(43): Show | 47 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.3180+49C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99987409 | ||||||
| chr8:99987434
|
T | G | 3 | a0001c0001t0001g0233a0001c0001t0001g0247a0011c0016t0001g0132 | 3 | HG01255.hp2 HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3180+24A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99987434 | ||||||
| chr8:99987440
|
T | C | 32 | a0000c0021t0001g0150a0001c0001t0001g0233a0001c0001t0001g0247others(29): Show | 32 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.3180+18A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 21/27 | chr8 | 99987440 | ||||||
| chr8:99988060
|
T | C | 18 | a0001c0001t0001g0118a0001c0001t0001g0129a0001c0001t0001g0284others(15): Show | 18 | HG00733.hp1 HG00738.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.3019-441A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99988060 | ||||||
| chr8:99988167
|
T | A | 30 | a0001c0001t0001g0022a0001c0001t0001g0048a0001c0001t0001g0049others(27): Show | 30 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.3019-548A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99988167 | ||||||
| chr8:99988880
|
C | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(4): Show | 7 | NA18955.hp1 NA18970.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.3019-1261G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99988880 | ||||||
| chr8:99989011
|
A | G | 3 | a0001c0001t0001g0233a0001c0001t0001g0247a0011c0016t0001g0132 | 3 | HG01255.hp2 HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3019-1392T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99989011 | ||||||
| chr8:99989058
|
T | A | 46 | a0000c0019t0001g0248a0001c0001t0001g0008a0001c0001t0001g0018others(43): Show | 47 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.3019-1439A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99989058 | ||||||
| chr8:99989324
|
A | G | 29 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(26): Show | 29 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.3019-1705T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99989324 | ||||||
| chr8:99989456
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3019-1837A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99989456 | ||||||
| chr8:99989476
|
C | A | 1 | a0001c0001t0001g0128 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3019-1857G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99989476 | ||||||
| chr8:99989595
|
G | C | 2 | a0001c0012t0001g0112a0001c0012t0001g0131 | 2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3019-1976C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99989595 | ||||||
| chr8:99989861
|
C | CAGAT | 93 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0017others(90): Show | 94 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.3019-2246_3019-224 others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99989861 | ||||||
| chr8:99989861
|
C | CAGATAGA others(1): Show |
15 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0048others(12): Show | 15 | HG01099.hp1 HG01109.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.3019-2250_3019-224 others(12): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99989861 | ||||||
| chr8:99989861
|
C | CAGATAGA others(5): Show |
2 | a0001c0001t0001g0282a0001c0001t0001g0285 | 2 | HG02027.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.3019-2254_3019-224 others(16): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99989861 | ||||||
| chr8:99989861
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3019-2242G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99989861 | ||||||
| chr8:99989861
|
CAGAT | C | 49 | a0000c0019t0001g0248a0001c0001t0001g0004a0001c0001t0001g0008others(46): Show | 50 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.3019-2246_3019-224 others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99989861 | ||||||
| chr8:99989861
|
CAGATAGA others(1): Show |
C | 3 | a0001c0001t0001g0219a0001c0012t0001g0112a0016c0025t0001g0307 | 3 | HG02145.hp2 NA18963.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.3019-2250_3019-224 others(12): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99989861 | ||||||
| chr8:99989861
|
CAGATAGA others(5): Show |
C | 1 | a0001c0003t0001g0064 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3019-2254_3019-224 others(16): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99989861 | ||||||
| chr8:99989878
|
A | AGATG | 4 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0190others(1): Show | 4 | NA18946.hp1 NA18953.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.3019-2260_3019-225 others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99989878 | ||||||
| chr8:99989905
|
T | TAG | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | NA18955.hp2 NA19005.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.3019-2287_3019-228 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99989905 | ||||||
| chr8:99989905
|
TATAG | T | 8 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0136others(5): Show | 8 | HG01243.hp2 HG01255.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.3019-2290_3019-228 others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99989905 | ||||||
| chr8:99989907
|
T | G | 1 | a0002c0002t0001g0289 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3019-2288A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99989907 | ||||||
| chr8:99989909
|
G | GAT | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | NA18955.hp2 NA19005.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.3019-2292_3019-229 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99989909 | ||||||
| chr8:99989909
|
G | T | 1 | a0002c0002t0001g0289 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3019-2290C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99989909 | ||||||
| chr8:99990171
|
C | T | 1 | a0002c0002t0001g0086 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3019-2552G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99990171 | ||||||
| chr8:99990226
|
C | T | 29 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(26): Show | 29 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.3019-2607G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99990226 | ||||||
| chr8:99990239
|
G | A | 2 | a0001c0001t0001g0102a0001c0003t0001g0055 | 2 | HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3019-2620C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99990239 | ||||||
| chr8:99990242
|
A | G | 2 | a0001c0012t0001g0112a0001c0012t0001g0131 | 2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3019-2623T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99990242 | ||||||
| chr8:99990280
|
A | G | 1 | a0001c0001t0001g0128 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3019-2661T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99990280 | ||||||
| chr8:99990341
|
G | T | 1 | a0001c0001t0001g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3019-2722C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99990341 | ||||||
| chr8:99990362
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3019-2743G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99990362 | ||||||
| chr8:99990456
|
G | A | 46 | a0000c0019t0001g0248a0001c0001t0001g0008a0001c0001t0001g0018others(43): Show | 47 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.3019-2837C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99990456 | ||||||
| chr8:99990489
|
C | T | 6 | a0001c0001t0001g0202a0001c0001t0001g0240a0001c0001t0001g0246others(3): Show | 6 | NA18968.hp1 NA18978.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.3019-2870G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99990489 | ||||||
| chr8:99990592
|
C | T | 80 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(77): Show | 80 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.3019-2973G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99990592 | ||||||
| chr8:99990634
|
T | C | 1 | a0012c0023t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3019-3015A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99990634 | ||||||
| chr8:99990645
|
G | A | 1 | a0003c0005t0001g0060 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3019-3026C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99990645 | ||||||
| chr8:99990767
|
C | T | 29 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(26): Show | 29 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.3019-3148G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99990767 | ||||||
| chr8:99990819
|
C | G | 3 | a0001c0001t0001g0233a0001c0001t0001g0247a0011c0016t0001g0132 | 3 | HG01255.hp2 HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3019-3200G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99990819 | ||||||
| chr8:99990879
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3019-3260C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99990879 | ||||||
| chr8:99990906
|
C | T | 80 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(77): Show | 80 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.3019-3287G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99990906 | ||||||
| chr8:99990966
|
C | G | 3 | a0001c0001t0001g0067a0001c0001t0001g0128a0001c0003t0001g0005 | 3 | HG03471.hp1 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3019-3347G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99990966 | ||||||
| chr8:99991103
|
T | A | 1 | a0001c0001t0001g0137 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.3019-3484A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99991103 | ||||||
| chr8:99991221
|
G | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0221 | 2 | NA18946.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.3019-3602C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99991221 | ||||||
| chr8:99991299
|
T | C | 210 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(207): Show | 212 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(209): Show |
intron_variant | MODIFIER | c.3019-3680A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99991299 | ||||||
| chr8:99991346
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0093 | 2 | NA19010.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.3019-3727G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99991346 | ||||||
| chr8:99991419
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3019-3800A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99991419 | ||||||
| chr8:99991461
|
G | A | 1 | a0001c0001t0001g0293 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3019-3842C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99991461 | ||||||
| chr8:99991462
|
C | T | 209 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(206): Show | 211 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(208): Show |
intron_variant | MODIFIER | c.3019-3843G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99991462 | ||||||
| chr8:99991476
|
G | A | 2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3019-3857C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99991476 | ||||||
| chr8:99991584
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3019-3965G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99991584 | ||||||
| chr8:99991632
|
A | G | 8 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0152others(5): Show | 8 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.3019-4013T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99991632 | ||||||
| chr8:99991664
|
G | C | 1 | a0012c0023t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3019-4045C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99991664 | ||||||
| chr8:99991911
|
A | G | 147 | a0000c0021t0001g0150a0001c0001t0001g0006a0001c0001t0001g0007others(144): Show | 148 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(145): Show |
intron_variant | MODIFIER | c.3019-4292T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99991911 | ||||||
| chr8:99992006
|
C | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0099 | 2 | HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3019-4387G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99992006 | ||||||
| chr8:99992152
|
G | C | 147 | a0000c0021t0001g0150a0001c0001t0001g0006a0001c0001t0001g0007others(144): Show | 148 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(145): Show |
intron_variant | MODIFIER | c.3018+4310C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99992152 | ||||||
| chr8:99992178
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3018+4284G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99992178 | ||||||
| chr8:99992288
|
G | A | 1 | a0012c0023t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3018+4174C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99992288 | ||||||
| chr8:99992394
|
T | C | 1 | a0001c0001t0001g0257 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.3018+4068A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99992394 | ||||||
| chr8:99992458
|
T | G | 210 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(207): Show | 212 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(209): Show |
intron_variant | MODIFIER | c.3018+4004A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99992458 | ||||||
| chr8:99992490
|
T | C | 77 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(74): Show | 77 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.3018+3972A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99992490 | ||||||
| chr8:99992525
|
G | A | 146 | a0000c0021t0001g0150a0001c0001t0001g0006a0001c0001t0001g0007others(143): Show | 147 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(144): Show |
intron_variant | MODIFIER | c.3018+3937C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99992525 | ||||||
| chr8:99992659
|
A | G | 3 | a0001c0001t0001g0067a0001c0001t0001g0128a0001c0003t0001g0005 | 3 | HG03471.hp1 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3018+3803T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99992659 | ||||||
| chr8:99992680
|
A | G | 29 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(26): Show | 29 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.3018+3782T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99992680 | ||||||
| chr8:99992792
|
C | T | 62 | a0000c0019t0001g0248a0001c0001t0001g0004a0001c0001t0001g0008others(59): Show | 63 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.3018+3670G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99992792 | ||||||
| chr8:99992834
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3018+3628G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99992834 | ||||||
| chr8:99992953
|
G | T | 3 | a0001c0001t0001g0233a0001c0001t0001g0247a0011c0016t0001g0132 | 3 | HG01255.hp2 HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3018+3509C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99992953 | ||||||
| chr8:99993030
|
G | A | 4 | a0001c0003t0001g0074a0001c0003t0001g0075a0001c0003t0001g0076others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.3018+3432C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99993030 | ||||||
| chr8:99993136
|
T | C | 1 | a0001c0012t0001g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3018+3326A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99993136 | ||||||
| chr8:99993190
|
C | T | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3018+3272G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99993190 | ||||||
| chr8:99993191
|
A | G | 3 | a0001c0001t0001g0233a0001c0001t0001g0247a0011c0016t0001g0132 | 3 | HG01255.hp2 HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3018+3271T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99993191 | ||||||
| chr8:99993479
|
A | G | 7 | a0001c0001t0001g0103a0001c0001t0001g0104a0003c0005t0001g0106others(4): Show | 7 | HG01884.hp2 HG02630.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.3018+2983T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99993479 | ||||||
| chr8:99993484
|
C | G | 1 | a0001c0001t0001g0167 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.3018+2978G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99993484 | ||||||
| chr8:99993687
|
C | T | 29 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(26): Show | 29 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.3018+2775G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99993687 | ||||||
| chr8:99993736
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3018+2726T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99993736 | ||||||
| chr8:99993850
|
G | C | 1 | a0001c0001t0001g0196 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3018+2612C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99993850 | ||||||
| chr8:99993935
|
T | C | 7 | a0001c0001t0001g0232a0001c0001t0001g0234a0001c0001t0001g0235others(4): Show | 7 | HG00408.hp2 NA18960.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.3018+2527A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99993935 | ||||||
| chr8:99994199
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3018+2263G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99994199 | ||||||
| chr8:99994235
|
A | G | 15 | a0001c0001t0001g0298a0003c0005t0001g0002a0003c0005t0001g0057others(12): Show | 16 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.3018+2227T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99994235 | ||||||
| chr8:99994465
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3018+1997A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99994465 | ||||||
| chr8:99994532
|
A | T | 29 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(26): Show | 29 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.3018+1930T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99994532 | ||||||
| chr8:99994644
|
C | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0295 | 2 | HG02738.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.3018+1818G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99994644 | ||||||
| chr8:99994779
|
C | T | 4 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(1): Show | 4 | HG01496.hp2 HG02004.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.3018+1683G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99994779 | ||||||
| chr8:99994890
|
A | G | 1 | a0012c0023t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3018+1572T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99994890 | ||||||
| chr8:99995071
|
A | T | 29 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(26): Show | 29 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.3018+1391T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99995071 | ||||||
| chr8:99995109
|
A | C | 46 | a0000c0019t0001g0248a0001c0001t0001g0008a0001c0001t0001g0018others(43): Show | 47 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.3018+1353T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99995109 | ||||||
| chr8:99995396
|
C | T | 46 | a0000c0019t0001g0248a0001c0001t0001g0008a0001c0001t0001g0018others(43): Show | 47 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.3018+1066G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99995396 | ||||||
| chr8:99995397
|
G | A | 4 | a0001c0001t0001g0233a0001c0001t0001g0247a0001c0001t0001g0284others(1): Show | 4 | HG01255.hp2 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3018+1065C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99995397 | ||||||
| chr8:99995406
|
A | G | 1 | a0001c0001t0003g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3018+1056T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99995406 | ||||||
| chr8:99995420
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3018+1042C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99995420 | ||||||
| chr8:99995441
|
A | G | 60 | a0000c0019t0001g0248a0001c0001t0001g0008a0001c0001t0001g0018others(57): Show | 61 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.3018+1021T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99995441 | ||||||
| chr8:99995449
|
G | A | 208 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(205): Show | 210 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(207): Show |
intron_variant | MODIFIER | c.3018+1013C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99995449 | ||||||
| chr8:99995487
|
A | G | 15 | a0001c0001t0001g0118a0001c0001t0001g0129a0001c0004t0002g0062others(12): Show | 15 | HG00733.hp1 HG00738.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.3018+975T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99995487 | ||||||
| chr8:99995697
|
G | T | 1 | a0001c0001t0001g0039 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3018+765C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99995697 | ||||||
| chr8:99995759
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.3018+703C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99995759 | ||||||
| chr8:99995791
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3018+671C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99995791 | ||||||
| chr8:99995966
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3018+496T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99995966 | ||||||
| chr8:99996115
|
G | T | 2 | a0005c0006t0001g0091a0005c0006t0001g0092 | 2 | NA18966.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.3018+347C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99996115 | ||||||
| chr8:99996239
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3018+223T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99996239 | ||||||
| chr8:99996428
|
T | A | 1 | a0001c0001t0001g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3018+34A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 20/27 | chr8 | 99996428 | ||||||
| chr8:99996571
|
T | G | 2 | a0001c0001t0001g0237a0001c0001t0001g0254 | 2 | NA18984.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.2950-41A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 19/27 | chr8 | 99996571 | ||||||
| chr8:99996640
|
T | C | 3 | a0001c0001t0001g0233a0001c0001t0001g0247a0011c0016t0001g0132 | 3 | HG01255.hp2 HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2950-110A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 19/27 | chr8 | 99996640 | ||||||
| chr8:99996783
|
A | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0099 | 2 | HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2950-253T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 19/27 | chr8 | 99996783 | ||||||
| chr8:99996802
|
C | T | 6 | a0001c0001t0001g0103a0001c0001t0001g0104a0006c0007t0001g0113others(3): Show | 6 | HG01884.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2950-272G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 19/27 | chr8 | 99996802 | ||||||
| chr8:99996829
|
C | G | 1 | a0001c0001t0001g0297 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2950-299G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 19/27 | chr8 | 99996829 | ||||||
| chr8:99996901
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2950-371T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 19/27 | chr8 | 99996901 | ||||||
| chr8:99997006
|
T | C | 31 | a0000c0021t0001g0150a0001c0012t0001g0112a0001c0012t0001g0131others(28): Show | 31 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.2950-476A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 19/27 | chr8 | 99997006 | ||||||
| chr8:99997170
|
A | G | 1 | a0001c0003t0001g0130 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2950-640T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 19/27 | chr8 | 99997170 | ||||||
| chr8:99997187
|
C | T | 29 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(26): Show | 29 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.2950-657G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 19/27 | chr8 | 99997187 | ||||||
| chr8:99997195
|
C | T | 226 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(223): Show | 228 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.2950-665G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 19/27 | chr8 | 99997195 | ||||||
| chr8:99997602
|
T | C | 1 | a0012c0023t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2950-1072A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 19/27 | chr8 | 99997602 | ||||||
| chr8:99997991
|
C | A | 1 | a0001c0001t0001g0008 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2949+1271G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 19/27 | chr8 | 99997991 | ||||||
| chr8:99998000
|
G | A | 156 | a0000c0019t0001g0248a0001c0001t0001g0004a0001c0001t0001g0008others(153): Show | 157 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.2949+1262C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 19/27 | chr8 | 99998000 | ||||||
| chr8:99998397
|
G | GT | 98 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0034others(95): Show | 98 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.2949+864dupA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 19/27 | chr8 | 99998397 | ||||||
| chr8:99998453
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2949+809G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 19/27 | chr8 | 99998453 | ||||||
| chr8:99998612
|
C | T | 2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2949+650G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 19/27 | chr8 | 99998612 | ||||||
| chr8:99998640
|
A | T | 1 | a0001c0001t0001g0004 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2949+622T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 19/27 | chr8 | 99998640 | ||||||
| chr8:99998882
|
C | A | 1 | a0001c0001t0003g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2949+380G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 19/27 | chr8 | 99998882 | ||||||
| chr8:99998888
|
G | A | 2 | a0001c0001t0001g0233a0001c0001t0001g0247 | 2 | HG01255.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2949+374C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 19/27 | chr8 | 99998888 | ||||||
| chr8:99998948
|
G | T | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2949+314C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 19/27 | chr8 | 99998948 | ||||||
| chr8:99998968
|
G | A | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2949+294C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 19/27 | chr8 | 99998968 | ||||||
| chr8:99999120
|
C | T | 46 | a0000c0019t0001g0248a0001c0001t0001g0008a0001c0001t0001g0018others(43): Show | 47 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.2949+142G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 19/27 | chr8 | 99999120 | ||||||
| chr8:99999158
|
T | TA | 28 | a0000c0019t0001g0248a0001c0001t0001g0008a0001c0001t0001g0018others(25): Show | 29 | HG00099.hp1 HG00673.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.2949+103dupT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 19/27 | chr8 | 99999158 | ||||||
| chr8:99999189
|
C | T | 29 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(26): Show | 29 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.2949+73G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 19/27 | chr8 | 99999189 | ||||||
| chr8:99999546
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0099 | 2 | HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2791-126C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 99999546 | ||||||
| chr8:99999599
|
A | C | 31 | a0000c0021t0001g0150a0001c0012t0001g0112a0001c0012t0001g0131others(28): Show | 31 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.2791-179T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 99999599 | ||||||
| chr8:99999793
|
T | C | 1 | a0002c0002t0001g0033 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2791-373A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 99999793 | ||||||
| chr8:99999910
|
G | A | 1 | a0001c0001t0001g0219 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2791-490C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 99999910 | ||||||
| chr8:100000022
|
A | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0233others(2): Show | 5 | HG01255.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2791-602T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100000022 | ||||||
| chr8:100000187
|
A | G | 1 | a0002c0002t0001g0155 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2791-767T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100000187 | ||||||
| chr8:100000193
|
C | T | 98 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0034others(95): Show | 98 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.2791-773G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100000193 | ||||||
| chr8:100000224
|
C | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0049 | 2 | NA18954.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.2791-804G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100000224 | ||||||
| chr8:100000427
|
A | C | 1 | a0001c0001t0001g0051 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2791-1007T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100000427 | ||||||
| chr8:100000548
|
G | T | 1 | a0001c0004t0002g0114 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2791-1128C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100000548 | ||||||
| chr8:100000581
|
A | G | 1 | a0001c0012t0001g0131 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2791-1161T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100000581 | ||||||
| chr8:100000685
|
T | C | 17 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0066others(14): Show | 17 | HG00597.hp2 HG02145.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.2791-1265A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100000685 | ||||||
| chr8:100000734
|
C | T | 15 | a0001c0001t0001g0118a0001c0001t0001g0129a0001c0004t0002g0062others(12): Show | 15 | HG00733.hp1 HG00738.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.2791-1314G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100000734 | ||||||
| chr8:100000754
|
C | T | 2 | a0001c0001t0001g0251a0001c0001t0001g0252 | 2 | HG00609.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.2791-1334G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100000754 | ||||||
| chr8:100001038
|
A | G | 1 | a0001c0001t0001g0231 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2790+1164T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100001038 | ||||||
| chr8:100001145
|
A | G | 146 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0022others(143): Show | 146 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.2790+1057T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100001145 | ||||||
| chr8:100001202
|
T | A | 1 | a0001c0001t0001g0159 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2790+1000A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100001202 | ||||||
| chr8:100001202
|
T | TTATA | 146 | a0000c0019t0001g0248a0001c0001t0001g0008a0001c0001t0001g0018others(143): Show | 147 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.2790+996_2790+999d others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100001202 | ||||||
| chr8:100001202
|
T | TTATATA | 6 | a0001c0001t0001g0073a0001c0001t0001g0135a0001c0001t0001g0136others(3): Show | 6 | HG02922.hp2 HG03098.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.2790+994_2790+999d others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100001202 | ||||||
| chr8:100001202
|
T | TTATATAT others(11): Show |
1 | a0001c0003t0001g0130 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2790+999_2790+1000 others(21): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100001202 | ||||||
| chr8:100001202
|
T | TTATATAT others(13): Show |
59 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(56): Show | 59 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.2790+980_2790+999d others(22): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100001202 | ||||||
| chr8:100001202
|
T | TTATATAT others(33): Show |
3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244 | 3 | HG01496.hp2 HG02004.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2790+999_2790+1000 others(43): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100001202 | ||||||
| chr8:100001202
|
T | TTATATAT others(15): Show |
42 | a0001c0001t0001g0118a0001c0001t0001g0129a0001c0001t0001g0232others(39): Show | 43 | HG00408.hp2 HG00733.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.2790+999_2790+1000 others(25): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100001202 | ||||||
| chr8:100001203
|
T | TATATATA others(13): Show |
1 | a0003c0005t0001g0061 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2790+998_2790+999i others(22): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100001203 | ||||||
| chr8:100001204
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2790+997_2790+998i others(14): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100001204 | ||||||
| chr8:100001219
|
T | TATAC | 28 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(25): Show | 28 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.2790+982_2790+983i others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100001219 | ||||||
| chr8:100001219
|
T | TATATATA others(9): Show |
2 | a0001c0001t0001g0004a0001c0001t0001g0099 | 2 | HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2790+982_2790+983i others(18): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100001219 | ||||||
| chr8:100001219
|
T | TATATATA others(11): Show |
1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2790+982_2790+983i others(20): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100001219 | ||||||
| chr8:100001221
|
C | T | 29 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(26): Show | 29 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.2790+981G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100001221 | ||||||
| chr8:100001235
|
C | T | 1 | a0001c0001t0001g0277 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2790+967G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100001235 | ||||||
| chr8:100001236
|
A | ATATACAT others(14): Show |
1 | a0001c0001t0001g0277 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2790+965_2790+966i others(23): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100001236 | ||||||
| chr8:100001236
|
AT | A | 98 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0034others(95): Show | 98 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.2790+965delA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100001236 | ||||||
| chr8:100001273
|
G | A | 29 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(26): Show | 29 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.2790+929C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100001273 | ||||||
| chr8:100001300
|
A | G | 9 | a0001c0001t0001g0280a0001c0003t0001g0078a0001c0003t0001g0079others(6): Show | 9 | HG00597.hp2 NA18612.hp2 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.2790+902T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100001300 | ||||||
| chr8:100001499
|
G | T | 15 | a0001c0001t0001g0298a0003c0005t0001g0002a0003c0005t0001g0057others(12): Show | 16 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.2790+703C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100001499 | ||||||
| chr8:100001524
|
A | G | 211 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(208): Show | 212 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.2790+678T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 18/27 | chr8 | 100001524 | ||||||
| chr8:100002514
|
C | T | 8 | a0001c0001t0001g0139a0001c0001t0001g0157a0001c0001t0001g0179others(5): Show | 8 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(5): Show |
intron_variant | MODIFIER | c.2628-150G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 17/27 | chr8 | 100002514 | ||||||
| chr8:100003814
|
T | C | 3 | a0001c0003t0001g0079a0001c0003t0001g0080a0001c0003t0001g0264 | 3 | NA18612.hp2 NA18950.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.2627+112A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 17/27 | chr8 | 100003814 | ||||||
| chr8:100004237
|
T | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0233others(2): Show | 5 | HG01255.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2455-139A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 16/27 | chr8 | 100004237 | ||||||
| chr8:100004445
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2455-347G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 16/27 | chr8 | 100004445 | ||||||
| chr8:100004576
|
A | C | 1 | a0001c0001t0001g0035 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2455-478T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 16/27 | chr8 | 100004576 | ||||||
| chr8:100004716
|
T | C | 97 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0034others(94): Show | 97 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.2455-618A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 16/27 | chr8 | 100004716 | ||||||
| chr8:100004739
|
T | TTTTATAA others(317): Show |
1 | a0003c0022t0002g0110 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2455-642_2455-641i others(326): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 16/27 | chr8 | 100004739 | ||||||
| chr8:100004783
|
T | C | 97 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0034others(94): Show | 97 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.2455-685A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 16/27 | chr8 | 100004783 | ||||||
| chr8:100004837
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2455-739G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 16/27 | chr8 | 100004837 | ||||||
| chr8:100004987
|
C | T | 4 | a0001c0001t0001g0067a0001c0001t0001g0098a0001c0001t0001g0128others(1): Show | 4 | HG01099.hp1 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2455-889G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 16/27 | chr8 | 100004987 | ||||||
| chr8:100005267
|
T | A | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020 | 3 | HG01257.hp1 HG01258.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.2454+750A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 16/27 | chr8 | 100005267 | ||||||
| chr8:100005276
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2454+741A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 16/27 | chr8 | 100005276 | ||||||
| chr8:100005389
|
A | T | 2 | a0001c0001t0001g0233a0001c0001t0001g0247 | 2 | HG01255.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2454+628T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 16/27 | chr8 | 100005389 | ||||||
| chr8:100005618
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0099 | 2 | HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2454+399C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 16/27 | chr8 | 100005618 | ||||||
| chr8:100005990
|
G | GT | 9 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0103others(6): Show | 9 | HG01884.hp2 HG02630.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.2454+26dupA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 16/27 | chr8 | 100005990 | ||||||
| chr8:100006309
|
A | G | 1 | a0001c0001t0001g0220 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2362-200T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 15/27 | chr8 | 100006309 | ||||||
| chr8:100006406
|
T | C | 1 | a0001c0012t0001g0131 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2362-297A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 15/27 | chr8 | 100006406 | ||||||
| chr8:100006530
|
TAA | T | 3 | a0006c0007t0001g0113a0006c0007t0001g0125a0006c0007t0001g0126 | 3 | HG01884.hp2 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2362-423_2362-422d others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 15/27 | chr8 | 100006530 | ||||||
| chr8:100006596
|
T | G | 1 | a0001c0003t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2362-487A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 15/27 | chr8 | 100006596 | ||||||
| chr8:100006836
|
A | C | 2 | a0001c0001t0001g0143a0001c0001t0001g0271 | 2 | HG00621.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.2362-727T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 15/27 | chr8 | 100006836 | ||||||
| chr8:100006930
|
C | CT | 32 | a0000c0021t0001g0150a0001c0001t0001g0067a0001c0001t0001g0128others(29): Show | 32 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.2362-822dupA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 15/27 | chr8 | 100006930 | ||||||
| chr8:100007280
|
G | C | 3 | a0001c0001t0001g0233a0001c0001t0001g0247a0010c0015t0001g0117 | 3 | HG01255.hp2 HG03540.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2361+1095C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 15/27 | chr8 | 100007280 | ||||||
| chr8:100007357
|
A | C | 1 | a0001c0001t0001g0219 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2361+1018T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 15/27 | chr8 | 100007357 | ||||||
| chr8:100007370
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2361+1005G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 15/27 | chr8 | 100007370 | ||||||
| chr8:100007437
|
A | G | 3 | a0001c0001t0001g0233a0001c0001t0001g0247a0010c0015t0001g0117 | 3 | HG01255.hp2 HG03540.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2361+938T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 15/27 | chr8 | 100007437 | ||||||
| chr8:100007549
|
A | C | 1 | a0001c0009t0001g0100 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2361+826T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 15/27 | chr8 | 100007549 | ||||||
| chr8:100007761
|
CAAT | C | 3 | a0001c0001t0001g0138a0001c0001t0001g0203a0001c0001t0001g0225 | 3 | HG01109.hp2 HG01517.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.2361+611_2361+613d others(5): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 15/27 | chr8 | 100007761 | ||||||
| chr8:100007787
|
GA | G | 14 | a0003c0005t0001g0002a0003c0005t0001g0057a0003c0005t0001g0059others(11): Show | 15 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.2361+587delT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 15/27 | chr8 | 100007787 | ||||||
| chr8:100007849
|
C | CA | 22 | a0001c0001t0001g0144a0001c0001t0001g0162a0001c0001t0001g0165others(19): Show | 22 | HG00408.hp1 HG01256.hp2 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.2361+525dupT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 15/27 | chr8 | 100007849 | ||||||
| chr8:100008189
|
C | G | 3 | a0001c0001t0001g0284a0001c0009t0001g0100a0001c0009t0001g0101 | 3 | HG02486.hp2 HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2361+186G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 15/27 | chr8 | 100008189 | ||||||
| chr8:100008195
|
G | A | 2 | a0010c0015t0001g0117a0011c0016t0001g0132 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2361+180C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 15/27 | chr8 | 100008195 | ||||||
| chr8:100008208
|
T | C | 2 | a0001c0001t0001g0290a0001c0001t0001g0292 | 2 | HG00738.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.2361+167A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 15/27 | chr8 | 100008208 | ||||||
| chr8:100008240
|
G | A | 4 | a0000c0019t0001g0248a0001c0001t0001g0282a0001c0001t0001g0285others(1): Show | 4 | HG00673.hp1 HG02027.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2361+135C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 15/27 | chr8 | 100008240 | ||||||
| chr8:100008320
|
C | G | 205 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.2361+55G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 15/27 | chr8 | 100008320 | ||||||
| chr8:100008344
|
T | C | 28 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(25): Show | 28 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.2361+31A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 15/27 | chr8 | 100008344 | ||||||
| chr8:100008738
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2167-169G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100008738 | ||||||
| chr8:100008739
|
G | A | 1 | a0010c0015t0001g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2167-170C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100008739 | ||||||
| chr8:100009011
|
A | C | 30 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(27): Show | 30 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.2167-442T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100009011 | ||||||
| chr8:100009018
|
C | T | 2 | a0010c0015t0001g0117a0011c0016t0001g0132 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2167-449G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100009018 | ||||||
| chr8:100009348
|
G | A | 18 | a0000c0019t0001g0248a0001c0001t0001g0118a0001c0001t0001g0129others(15): Show | 18 | HG00673.hp1 HG00733.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.2167-779C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100009348 | ||||||
| chr8:100009424
|
C | CA | 14 | a0001c0001t0001g0073a0001c0001t0001g0098a0001c0001t0001g0134others(11): Show | 14 | HG01071.hp1 HG01099.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.2167-856dupT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100009424 | ||||||
| chr8:100009424
|
C | CAA | 25 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(22): Show | 25 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.2167-857_2167-856d others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100009424 | ||||||
| chr8:100009424
|
CA | C | 8 | a0001c0001t0001g0010a0001c0001t0001g0048a0001c0001t0001g0210others(5): Show | 8 | HG01243.hp2 HG01256.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.2167-856delT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100009424 | ||||||
| chr8:100009439
|
A | AG | 5 | a0001c0001t0001g0067a0001c0001t0001g0128a0001c0001t0001g0233others(2): Show | 5 | HG01255.hp2 HG03471.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2167-871_2167-870i others(3): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100009439 | ||||||
| chr8:100009485
|
G | A | 3 | a0001c0001t0001g0284a0001c0009t0001g0100a0001c0009t0001g0101 | 3 | HG02486.hp2 HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2167-916C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100009485 | ||||||
| chr8:100009729
|
A | C | 175 | a0000c0019t0001g0248a0001c0001t0001g0004a0001c0001t0001g0008others(172): Show | 175 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.2167-1160T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100009729 | ||||||
| chr8:100009730
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2167-1161C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100009730 | ||||||
| chr8:100009794
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2167-1225C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100009794 | ||||||
| chr8:100009860
|
G | T | 1 | a0001c0001t0001g0042 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2167-1291C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100009860 | ||||||
| chr8:100009891
|
G | A | 1 | a0001c0012t0001g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2167-1322C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100009891 | ||||||
| chr8:100009902
|
T | C | 16 | a0003c0005t0001g0002a0003c0005t0001g0057a0003c0005t0001g0059others(13): Show | 17 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.2167-1333A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100009902 | ||||||
| chr8:100009962
|
C | T | 16 | a0003c0005t0001g0002a0003c0005t0001g0057a0003c0005t0001g0059others(13): Show | 17 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.2167-1393G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100009962 | ||||||
| chr8:100010153
|
C | T | 16 | a0001c0001t0001g0030a0001c0001t0001g0035a0001c0001t0001g0038others(13): Show | 16 | HG00099.hp1 HG01071.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.2167-1584G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100010153 | ||||||
| chr8:100010157
|
C | T | 5 | a0001c0001t0001g0103a0001c0001t0001g0104a0006c0007t0001g0113others(2): Show | 5 | HG01884.hp2 HG02630.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2167-1588G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100010157 | ||||||
| chr8:100010253
|
C | T | 3 | a0001c0001t0001g0284a0001c0009t0001g0100a0001c0009t0001g0101 | 3 | HG02486.hp2 HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2167-1684G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100010253 | ||||||
| chr8:100010254
|
G | A | 6 | a0001c0001t0001g0067a0001c0001t0001g0098a0001c0001t0001g0128others(3): Show | 6 | HG01099.hp1 HG01255.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.2167-1685C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100010254 | ||||||
| chr8:100010303
|
T | G | 1 | a0002c0002t0001g0133 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2167-1734A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100010303 | ||||||
| chr8:100010512
|
C | T | 57 | a0000c0019t0001g0248a0001c0001t0001g0008a0001c0001t0001g0018others(54): Show | 57 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.2167-1943G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100010512 | ||||||
| chr8:100010583
|
T | A | 1 | a0001c0004t0002g0123 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2167-2014A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100010583 | ||||||
| chr8:100010754
|
G | T | 3 | a0001c0001t0001g0284a0001c0009t0001g0100a0001c0009t0001g0101 | 3 | HG02486.hp2 HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2167-2185C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100010754 | ||||||
| chr8:100010808
|
CT | C | 12 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0030others(9): Show | 12 | HG01243.hp2 HG01256.hp1 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.2167-2240delA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100010808 | ||||||
| chr8:100010825
|
A | G | 2 | a0001c0001t0001g0233a0001c0001t0001g0247 | 2 | HG01255.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2167-2256T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100010825 | ||||||
| chr8:100010864
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2167-2295C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100010864 | ||||||
| chr8:100011007
|
G | C | 1 | a0001c0001t0001g0301 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2167-2438C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100011007 | ||||||
| chr8:100011026
|
C | T | 29 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(26): Show | 29 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.2167-2457G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100011026 | ||||||
| chr8:100011027
|
G | A | 1 | a0001c0001t0003g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2167-2458C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100011027 | ||||||
| chr8:100011161
|
G | C | 1 | a0001c0001t0001g0276 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2167-2592C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100011161 | ||||||
| chr8:100011590
|
A | G | 3 | a0001c0001t0001g0284a0001c0009t0001g0100a0001c0009t0001g0101 | 3 | HG02486.hp2 HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2167-3021T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100011590 | ||||||
| chr8:100011879
|
A | G | 224 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(221): Show | 225 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.2167-3310T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100011879 | ||||||
| chr8:100011914
|
T | C | 1 | a0001c0001t0003g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2167-3345A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100011914 | ||||||
| chr8:100011951
|
G | T | 1 | a0001c0001t0003g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2167-3382C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100011951 | ||||||
| chr8:100012099
|
T | TTA | 28 | a0000c0021t0001g0150a0001c0001t0001g0275a0002c0002t0001g0033others(25): Show | 28 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.2167-3532_2167-353 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100012099 | ||||||
| chr8:100012101
|
A | T | 3 | a0003c0005t0001g0057a0003c0005t0001g0068a0008c0013t0001g0089 | 3 | HG02559.hp2 HG03041.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2167-3532T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100012101 | ||||||
| chr8:100012277
|
A | C | 57 | a0000c0019t0001g0248a0001c0001t0001g0008a0001c0001t0001g0018others(54): Show | 57 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.2167-3708T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100012277 | ||||||
| chr8:100012550
|
C | G | 1 | a0001c0001t0001g0065 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2167-3981G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100012550 | ||||||
| chr8:100012593
|
G | A | 2 | a0010c0015t0001g0117a0011c0016t0001g0132 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2167-4024C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100012593 | ||||||
| chr8:100012666
|
T | A | 1 | a0001c0001t0001g0038 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2167-4097A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100012666 | ||||||
| chr8:100012751
|
A | G | 1 | a0010c0015t0001g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2167-4182T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100012751 | ||||||
| chr8:100012965
|
G | T | 2 | a0010c0015t0001g0117a0011c0016t0001g0132 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2167-4396C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100012965 | ||||||
| chr8:100012978
|
A | AT | 12 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0043others(9): Show | 12 | HG00438.hp2 HG00735.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.2167-4410dupA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100012978 | ||||||
| chr8:100012978
|
AT | A | 120 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0034others(117): Show | 121 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.2167-4410delA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100012978 | ||||||
| chr8:100012978
|
ATT | A | 55 | a0000c0019t0001g0248a0001c0001t0001g0008a0001c0001t0001g0018others(52): Show | 55 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.2167-4411_2167-441 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100012978 | ||||||
| chr8:100013021
|
G | A | 3 | a0001c0001t0001g0067a0001c0001t0001g0128a0001c0003t0001g0005 | 3 | HG03471.hp1 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2167-4452C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100013021 | ||||||
| chr8:100013066
|
T | C | 208 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.2167-4497A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100013066 | ||||||
| chr8:100013206
|
G | A | 3 | a0001c0001t0001g0198a0001c0001t0001g0215a0001c0001t0001g0294 | 3 | HG00099.hp2 HG02698.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.2167-4637C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100013206 | ||||||
| chr8:100013403
|
C | T | 57 | a0000c0019t0001g0248a0001c0001t0001g0008a0001c0001t0001g0018others(54): Show | 57 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.2167-4834G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100013403 | ||||||
| chr8:100013582
|
T | C | 6 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0302others(3): Show | 6 | NA18960.hp1 NA18977.hp1 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.2167-5013A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100013582 | ||||||
| chr8:100013594
|
T | C | 1 | a0001c0003t0001g0214 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2167-5025A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100013594 | ||||||
| chr8:100013596
|
G | T | 1 | a0001c0003t0001g0214 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2167-5027C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100013596 | ||||||
| chr8:100013770
|
C | T | 204 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.2167-5201G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100013770 | ||||||
| chr8:100013877
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2167-5308G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100013877 | ||||||
| chr8:100013946
|
A | G | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2167-5377T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100013946 | ||||||
| chr8:100014210
|
C | T | 1 | a0001c0001t0001g0297 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2167-5641G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100014210 | ||||||
| chr8:100014211
|
G | A | 1 | a0001c0004t0002g0124 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2167-5642C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100014211 | ||||||
| chr8:100014235
|
A | C | 2 | a0001c0001t0001g0282a0001c0001t0001g0285 | 2 | HG02027.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.2167-5666T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100014235 | ||||||
| chr8:100014497
|
G | A | 85 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0001g0036others(82): Show | 85 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.2167-5928C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100014497 | ||||||
| chr8:100014517
|
C | T | 1 | a0010c0015t0001g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2167-5948G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100014517 | ||||||
| chr8:100014678
|
C | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020 | 3 | HG01257.hp1 HG01258.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.2167-6109G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100014678 | ||||||
| chr8:100014845
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2167-6276C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100014845 | ||||||
| chr8:100015082
|
A | C | 1 | a0001c0001t0001g0066 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2167-6513T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100015082 | ||||||
| chr8:100015234
|
C | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0093 | 2 | NA19010.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.2167-6665G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100015234 | ||||||
| chr8:100015289
|
T | TTTTC | 11 | a0001c0001t0001g0022a0001c0001t0001g0145a0001c0001t0001g0158others(8): Show | 11 | HG00621.hp1 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.2167-6724_2167-672 others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100015289 | ||||||
| chr8:100015380
|
C | A | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2167-6811G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100015380 | ||||||
| chr8:100015449
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2167-6880G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100015449 | ||||||
| chr8:100015456
|
C | G | 27 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(24): Show | 27 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.2167-6887G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100015456 | ||||||
| chr8:100015572
|
T | C | 1 | a0002c0002t0001g0149 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2167-7003A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100015572 | ||||||
| chr8:100015615
|
C | T | 1 | a0001c0001t0004g0142 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2167-7046G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100015615 | ||||||
| chr8:100015618
|
T | C | 1 | a0001c0001t0001g0225 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2167-7049A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100015618 | ||||||
| chr8:100015667
|
T | A | 208 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.2167-7098A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100015667 | ||||||
| chr8:100015817
|
G | T | 17 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0066others(14): Show | 17 | HG00597.hp2 HG02145.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.2167-7248C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100015817 | ||||||
| chr8:100016011
|
G | A | 57 | a0000c0019t0001g0248a0001c0001t0001g0008a0001c0001t0001g0018others(54): Show | 57 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.2167-7442C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100016011 | ||||||
| chr8:100016037
|
C | T | 3 | a0001c0001t0001g0284a0001c0009t0001g0100a0001c0009t0001g0101 | 3 | HG02486.hp2 HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2167-7468G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100016037 | ||||||
| chr8:100016131
|
A | T | 10 | a0001c0001t0001g0178a0001c0001t0001g0183a0001c0001t0001g0187others(7): Show | 10 | HG00099.hp2 HG00733.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.2167-7562T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100016131 | ||||||
| chr8:100016187
|
T | A | 174 | a0000c0019t0001g0248a0001c0001t0001g0004a0001c0001t0001g0008others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.2167-7618A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100016187 | ||||||
| chr8:100016371
|
C | CT | 179 | a0000c0019t0001g0248a0001c0001t0001g0004a0001c0001t0001g0008others(176): Show | 179 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.2167-7803dupA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100016371 | ||||||
| chr8:100016393
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2167-7824T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100016393 | ||||||
| chr8:100016452
|
C | T | 26 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(23): Show | 26 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.2167-7883G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100016452 | ||||||
| chr8:100016692
|
G | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0221 | 2 | NA18946.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.2167-8123C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100016692 | ||||||
| chr8:100016693
|
C | T | 31 | a0000c0021t0001g0150a0001c0001t0001g0035a0001c0001t0001g0038others(28): Show | 31 | HG00558.hp2 HG00673.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.2167-8124G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100016693 | ||||||
| chr8:100016754
|
G | A | 1 | a0003c0022t0002g0110 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2167-8185C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100016754 | ||||||
| chr8:100016830
|
G | A | 2 | a0001c0001t0001g0268a0001c0001t0001g0273 | 2 | HG01433.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2167-8261C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100016830 | ||||||
| chr8:100016861
|
C | T | 3 | a0001c0001t0001g0067a0001c0001t0001g0128a0001c0003t0001g0005 | 3 | HG03471.hp1 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2167-8292G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100016861 | ||||||
| chr8:100016978
|
C | CT | 39 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0024others(36): Show | 39 | HG00438.hp2 HG00621.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.2167-8410dupA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100016978 | ||||||
| chr8:100016978
|
C | CTT | 21 | a0000c0021t0001g0150a0001c0001t0001g0011a0001c0001t0001g0166others(18): Show | 21 | HG00558.hp2 HG00673.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.2167-8411_2167-841 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100016978 | ||||||
| chr8:100016978
|
CT | C | 26 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0090others(23): Show | 26 | HG00099.hp2 HG00621.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.2167-8410delA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100016978 | ||||||
| chr8:100016978
|
CTT | C | 39 | a0001c0001t0001g0098a0001c0001t0001g0118a0001c0001t0001g0138others(36): Show | 39 | HG00733.hp1 HG00733.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.2167-8411_2167-841 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100016978 | ||||||
| chr8:100016978
|
CTTT | C | 51 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0034others(48): Show | 51 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.2167-8412_2167-841 others(7): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100016978 | ||||||
| chr8:100016978
|
CTTTT | C | 12 | a0000c0019t0001g0248a0001c0001t0001g0067a0001c0001t0001g0129others(9): Show | 12 | HG00673.hp1 HG01074.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.2167-8413_2167-841 others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100016978 | ||||||
| chr8:100016978
|
CTTTTT | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0040others(7): Show | 10 | HG01517.hp1 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.2167-8414_2167-841 others(9): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100016978 | ||||||
| chr8:100016978
|
CTTTTTT | C | 14 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(11): Show | 14 | HG01071.hp2 HG01255.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.2167-8415_2167-841 others(10): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100016978 | ||||||
| chr8:100016978
|
CTTTTTTT | C | 14 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0042others(11): Show | 14 | HG00099.hp1 HG00558.hp1 HG00597.hp2 others(11): Show |
intron_variant | MODIFIER | c.2167-8416_2167-841 others(11): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100016978 | ||||||
| chr8:100016978
|
CTTTTTTT others(1): Show |
C | 10 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0019others(7): Show | 10 | HG01257.hp1 HG01258.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.2167-8417_2167-841 others(12): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100016978 | ||||||
| chr8:100016978
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2167-8419_2167-841 others(14): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100016978 | ||||||
| chr8:100016978
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0222 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2167-8423_2167-841 others(18): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100016978 | ||||||
| chr8:100016978
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0028 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2167-8425_2167-841 others(20): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100016978 | ||||||
| chr8:100016978
|
CTTTTTTT others(10): Show |
C | 8 | a0001c0001t0001g0180a0001c0001t0001g0297a0003c0005t0001g0057others(5): Show | 8 | HG02559.hp2 HG03041.hp2 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.2167-8426_2167-841 others(21): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100016978 | ||||||
| chr8:100016978
|
CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0001g0139 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2167-8427_2167-841 others(22): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100016978 | ||||||
| chr8:100016978
|
CTTTTTTT others(13): Show |
C | 1 | a0001c0001t0003g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2167-8429_2167-841 others(24): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100016978 | ||||||
| chr8:100017016
|
T | A | 1 | a0001c0001t0001g0285 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2167-8447A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100017016 | ||||||
| chr8:100017042
|
C | T | 3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045 | 3 | HG00735.hp2 HG01081.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2167-8473G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100017042 | ||||||
| chr8:100017153
|
T | C | 1 | a0001c0001t0001g0263 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2167-8584A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100017153 | ||||||
| chr8:100017603
|
T | C | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2167-9034A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100017603 | ||||||
| chr8:100017611
|
T | C | 27 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(24): Show | 27 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.2167-9042A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100017611 | ||||||
| chr8:100017968
|
C | A | 1 | a0001c0001t0001g0129 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2167-9399G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100017968 | ||||||
| chr8:100017996
|
T | G | 2 | a0003c0005t0001g0002a0003c0005t0001g0109 | 3 | HG02486.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2167-9427A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100017996 | ||||||
| chr8:100018017
|
C | G | 2 | a0010c0015t0001g0117a0011c0016t0001g0132 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2167-9448G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100018017 | ||||||
| chr8:100018159
|
T | G | 29 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(26): Show | 29 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.2167-9590A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100018159 | ||||||
| chr8:100018212
|
CA | C | 176 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0010others(173): Show | 176 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.2167-9644delT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100018212 | ||||||
| chr8:100018212
|
CAA | C | 28 | a0000c0021t0001g0150a0001c0003t0001g0079a0002c0002t0001g0033others(25): Show | 28 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.2167-9645_2167-964 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100018212 | ||||||
| chr8:100018361
|
T | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0028 | 2 | HG02300.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2167-9792A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100018361 | ||||||
| chr8:100018429
|
GAC | G | 7 | a0001c0001t0001g0067a0001c0001t0001g0134a0001c0001t0001g0284others(4): Show | 7 | HG01109.hp1 HG01243.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2167-9862_2167-986 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100018429 | ||||||
| chr8:100018429
|
GACAC | G | 201 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.2167-9864_2167-986 others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100018429 | ||||||
| chr8:100018457
|
T | C | 224 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(221): Show | 225 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.2167-9888A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100018457 | ||||||
| chr8:100018989
|
C | CA | 284 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0006others(281): Show | 286 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.2167-10421dupT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100018989 | ||||||
| chr8:100018989
|
C | CAA | 11 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0103others(8): Show | 11 | HG01884.hp2 HG02630.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.2167-10422_2167-10 others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100018989 | ||||||
| chr8:100019177
|
A | G | 30 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0137others(27): Show | 30 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.2167-10608T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100019177 | ||||||
| chr8:100019354
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2167-10785G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100019354 | ||||||
| chr8:100019647
|
T | C | 1 | a0001c0001t0001g0253 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2167-11078A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100019647 | ||||||
| chr8:100019732
|
C | T | 1 | a0001c0001t0001g0249 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2167-11163G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100019732 | ||||||
| chr8:100019853
|
G | C | 28 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(25): Show | 28 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.2167-11284C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100019853 | ||||||
| chr8:100019889
|
T | G | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2167-11320A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100019889 | ||||||
| chr8:100019945
|
TGCAATCT others(9): Show |
T | 172 | a0000c0019t0001g0248a0001c0001t0001g0004a0001c0001t0001g0008others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.2167-11392_2167-11 others(22): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100019945 | ||||||
| chr8:100019971
|
G | A | 67 | a0000c0019t0001g0248a0001c0001t0001g0004a0001c0001t0001g0008others(64): Show | 67 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.2167-11402C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100019971 | ||||||
| chr8:100020130
|
C | T | 28 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(25): Show | 28 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.2167-11561G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100020130 | ||||||
| chr8:100020269
|
C | T | 4 | a0001c0001t0001g0067a0001c0001t0001g0134a0001c0001t0003g0003others(1): Show | 4 | HG01109.hp1 HG01243.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2167-11700G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100020269 | ||||||
| chr8:100020316
|
C | T | 2 | a0001c0012t0001g0112a0001c0012t0001g0131 | 2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2167-11747G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100020316 | ||||||
| chr8:100020320
|
C | G | 1 | a0001c0001t0001g0030 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2167-11751G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100020320 | ||||||
| chr8:100020419
|
G | A | 22 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0019others(19): Show | 22 | HG00099.hp1 HG01071.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.2167-11850C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100020419 | ||||||
| chr8:100020464
|
A | G | 28 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(25): Show | 28 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.2167-11895T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100020464 | ||||||
| chr8:100020525
|
C | A | 1 | a0001c0001t0001g0032 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2167-11956G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100020525 | ||||||
| chr8:100020683
|
T | C | 28 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(25): Show | 28 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.2167-12114A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100020683 | ||||||
| chr8:100020946
|
C | T | 202 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.2167-12377G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100020946 | ||||||
| chr8:100020957
|
T | A | 1 | a0001c0001t0001g0195 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2167-12388A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100020957 | ||||||
| chr8:100021072
|
G | A | 1 | a0001c0003t0001g0009 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2167-12503C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100021072 | ||||||
| chr8:100021165
|
G | T | 2 | a0001c0001t0001g0067a0001c0003t0001g0005 | 2 | HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2167-12596C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100021165 | ||||||
| chr8:100021509
|
G | A | 195 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0008others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.2167-12940C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100021509 | ||||||
| chr8:100021559
|
T | A | 1 | a0001c0001t0001g0263 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2167-12990A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100021559 | ||||||
| chr8:100021670
|
G | A | 3 | a0001c0001t0001g0284a0001c0009t0001g0100a0001c0009t0001g0101 | 3 | HG02486.hp2 HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2167-13101C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100021670 | ||||||
| chr8:100021708
|
C | T | 6 | a0001c0001t0001g0172a0001c0001t0001g0177a0001c0001t0001g0194others(3): Show | 6 | HG01433.hp1 HG01934.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.2167-13139G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100021708 | ||||||
| chr8:100021711
|
G | C | 3 | a0003c0005t0001g0069a0003c0005t0001g0107a0003c0005t0001g0108 | 3 | HG02717.hp1 HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2167-13142C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100021711 | ||||||
| chr8:100021781
|
G | GA | 29 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(26): Show | 29 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.2167-13213dupT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100021781 | ||||||
| chr8:100021840
|
A | C | 1 | a0003c0005t0001g0061 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2167-13271T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100021840 | ||||||
| chr8:100022237
|
A | G | 2 | a0001c0001t0001g0067a0001c0003t0001g0005 | 2 | HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2167-13668T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100022237 | ||||||
| chr8:100022408
|
C | T | 2 | a0001c0001t0001g0290a0001c0001t0001g0292 | 2 | HG00738.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.2167-13839G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100022408 | ||||||
| chr8:100022427
|
A | G | 28 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(25): Show | 28 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.2167-13858T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100022427 | ||||||
| chr8:100022656
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2167-14087T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100022656 | ||||||
| chr8:100022657
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2167-14088G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100022657 | ||||||
| chr8:100022733
|
A | C | 1 | a0001c0001t0001g0144 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2167-14164T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100022733 | ||||||
| chr8:100022746
|
A | T | 5 | a0001c0001t0001g0047a0001c0001t0001g0098a0001c0001t0001g0298others(2): Show | 5 | HG01099.hp1 HG01243.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2167-14177T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100022746 | ||||||
| chr8:100022748
|
T | C | 2 | a0002c0002t0001g0087a0002c0002t0001g0088 | 2 | NA18946.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.2167-14179A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100022748 | ||||||
| chr8:100022750
|
T | A | 32 | a0000c0019t0001g0248a0001c0001t0001g0004a0001c0001t0001g0016others(29): Show | 33 | HG00621.hp2 HG00673.hp1 HG02027.hp1 others(30): Show |
intron_variant | MODIFIER | c.2167-14181A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100022750 | ||||||
| chr8:100022754
|
T | A | 2 | a0003c0005t0001g0106a0012c0023t0003g0105 | 2 | HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2167-14185A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100022754 | ||||||
| chr8:100022968
|
G | A | 2 | a0001c0001t0001g0233a0001c0001t0001g0247 | 2 | HG01255.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2167-14399C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100022968 | ||||||
| chr8:100023518
|
C | T | 3 | a0001c0001t0001g0098a0001c0001t0001g0233a0001c0001t0001g0247 | 3 | HG01099.hp1 HG01255.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2167-14949G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100023518 | ||||||
| chr8:100023607
|
T | A | 58 | a0000c0019t0001g0248a0001c0001t0001g0008a0001c0001t0001g0018others(55): Show | 58 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.2167-15038A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100023607 | ||||||
| chr8:100023802
|
G | C | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG01071.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.2166+15129C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100023802 | ||||||
| chr8:100023821
|
T | C | 2 | a0002c0002t0001g0155a0002c0002t0001g0156 | 2 | HG00558.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.2166+15110A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100023821 | ||||||
| chr8:100024089
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2166+14842C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100024089 | ||||||
| chr8:100024124
|
G | A | 58 | a0000c0019t0001g0248a0001c0001t0001g0008a0001c0001t0001g0018others(55): Show | 58 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.2166+14807C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100024124 | ||||||
| chr8:100024128
|
G | A | 3 | a0001c0001t0001g0284a0001c0009t0001g0100a0001c0009t0001g0101 | 3 | HG02486.hp2 HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2166+14803C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100024128 | ||||||
| chr8:100024371
|
ACACT | A | 7 | a0001c0001t0001g0102a0001c0003t0001g0001a0001c0003t0001g0052others(4): Show | 8 | HG02109.hp1 HG02257.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.2166+14556_2166+14 others(10): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100024371 | ||||||
| chr8:100024496
|
AT | A | 16 | a0003c0005t0001g0002a0003c0005t0001g0057a0003c0005t0001g0059others(13): Show | 17 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.2166+14434delA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100024496 | ||||||
| chr8:100024586
|
G | T | 1 | a0001c0001t0001g0031 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2166+14345C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100024586 | ||||||
| chr8:100024777
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2166+14154C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100024777 | ||||||
| chr8:100025001
|
T | C | 1 | a0001c0001t0001g0201 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2166+13930A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100025001 | ||||||
| chr8:100025003
|
T | TATAA | 157 | a0000c0019t0001g0248a0001c0001t0001g0004a0001c0001t0001g0008others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.2166+13924_2166+13 others(10): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100025003 | ||||||
| chr8:100025003
|
T | TATAAATA others(1): Show |
20 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0037others(17): Show | 20 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.2166+13920_2166+13 others(14): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100025003 | ||||||
| chr8:100025003
|
T | TATAAATA others(5): Show |
1 | a0002c0011t0001g0071 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2166+13916_2166+13 others(18): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100025003 | ||||||
| chr8:100025003
|
TATAAATA others(1): Show |
T | 27 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(24): Show | 27 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.2166+13920_2166+13 others(14): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100025003 | ||||||
| chr8:100025003
|
TATAAATA others(5): Show |
T | 1 | a0010c0015t0001g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2166+13916_2166+13 others(18): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100025003 | ||||||
| chr8:100025363
|
T | C | 27 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(24): Show | 27 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.2166+13568A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100025363 | ||||||
| chr8:100025559
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2166+13372G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100025559 | ||||||
| chr8:100025581
|
C | T | 2 | a0001c0001t0001g0030a0011c0016t0001g0132 | 2 | HG03225.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.2166+13350G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100025581 | ||||||
| chr8:100025815
|
T | C | 1 | a0001c0003t0001g0078 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2166+13116A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100025815 | ||||||
| chr8:100026148
|
T | C | 3 | a0001c0001t0001g0284a0001c0009t0001g0100a0001c0009t0001g0101 | 3 | HG02486.hp2 HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2166+12783A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100026148 | ||||||
| chr8:100026243
|
C | T | 1 | a0016c0025t0001g0307 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2166+12688G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100026243 | ||||||
| chr8:100026411
|
ATT | A | 27 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(24): Show | 27 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.2166+12518_2166+12 others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100026411 | ||||||
| chr8:100026773
|
A | C | 1 | a0001c0003t0001g0077 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2166+12158T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100026773 | ||||||
| chr8:100026857
|
G | A | 2 | a0001c0001t0001g0145a0009c0014t0001g0146 | 2 | HG03654.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.2166+12074C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100026857 | ||||||
| chr8:100026864
|
T | TA | 29 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(26): Show | 29 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.2166+12066dupT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100026864 | ||||||
| chr8:100026927
|
T | C | 1 | a0001c0001t0001g0006 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2166+12004A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100026927 | ||||||
| chr8:100027008
|
T | C | 172 | a0000c0019t0001g0248a0001c0001t0001g0004a0001c0001t0001g0008others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.2166+11923A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100027008 | ||||||
| chr8:100027016
|
G | A | 5 | a0001c0001t0001g0103a0001c0001t0001g0104a0006c0007t0001g0113others(2): Show | 5 | HG01884.hp2 HG02630.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2166+11915C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100027016 | ||||||
| chr8:100027029
|
A | C | 1 | a0001c0001t0001g0251 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2166+11902T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100027029 | ||||||
| chr8:100027073
|
T | C | 5 | a0001c0001t0001g0256a0001c0001t0001g0258a0001c0003t0001g0064others(2): Show | 5 | HG02630.hp2 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2166+11858A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100027073 | ||||||
| chr8:100027080
|
G | C | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2166+11851C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100027080 | ||||||
| chr8:100027127
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2166+11804C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100027127 | ||||||
| chr8:100027458
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2166+11473G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100027458 | ||||||
| chr8:100027605
|
T | C | 201 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.2166+11326A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100027605 | ||||||
| chr8:100027769
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2166+11162G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100027769 | ||||||
| chr8:100027970
|
C | A | 3 | a0001c0001t0001g0284a0001c0009t0001g0100a0001c0009t0001g0101 | 3 | HG02486.hp2 HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2166+10961G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100027970 | ||||||
| chr8:100028455
|
C | CA | 25 | a0001c0001t0001g0182a0001c0001t0001g0194a0001c0001t0001g0204others(22): Show | 26 | HG01074.hp1 HG01099.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.2166+10475dupT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100028455 | ||||||
| chr8:100028455
|
CA | C | 71 | a0000c0019t0001g0248a0001c0001t0001g0004a0001c0001t0001g0008others(68): Show | 71 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.2166+10475delT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100028455 | ||||||
| chr8:100028455
|
CAA | C | 27 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(24): Show | 27 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.2166+10474_2166+10 others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100028455 | ||||||
| chr8:100028471
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2166+10460T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100028471 | ||||||
| chr8:100028473
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2166+10458C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100028473 | ||||||
| chr8:100028507
|
C | T | 1 | a0003c0005t0001g0059 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2166+10424G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100028507 | ||||||
| chr8:100028597
|
T | G | 208 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.2166+10334A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100028597 | ||||||
| chr8:100028619
|
G | A | 8 | a0002c0002t0001g0058a0002c0002t0001g0081a0002c0002t0001g0083others(5): Show | 8 | HG01081.hp1 NA18944.hp2 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.2166+10312C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100028619 | ||||||
| chr8:100028626
|
A | G | 8 | a0002c0002t0001g0058a0002c0002t0001g0081a0002c0002t0001g0083others(5): Show | 8 | HG01081.hp1 NA18944.hp2 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.2166+10305T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100028626 | ||||||
| chr8:100028682
|
C | T | 27 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(24): Show | 27 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.2166+10249G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100028682 | ||||||
| chr8:100028805
|
C | T | 13 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0149others(10): Show | 13 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.2166+10126G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100028805 | ||||||
| chr8:100028903
|
C | T | 27 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(24): Show | 27 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.2166+10028G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100028903 | ||||||
| chr8:100029131
|
C | G | 1 | a0001c0001t0001g0159 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2166+9800G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100029131 | ||||||
| chr8:100029416
|
A | G | 224 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(221): Show | 225 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.2166+9515T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100029416 | ||||||
| chr8:100029505
|
C | G | 1 | a0001c0001t0003g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2166+9426G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100029505 | ||||||
| chr8:100029531
|
G | A | 2 | a0001c0001t0001g0168a0007c0010t0001g0291 | 2 | NA18968.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.2166+9400C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100029531 | ||||||
| chr8:100029639
|
A | G | 205 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.2166+9292T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100029639 | ||||||
| chr8:100029702
|
C | CA | 67 | a0000c0019t0001g0248a0001c0001t0001g0004a0001c0001t0001g0008others(64): Show | 67 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.2166+9228dupT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100029702 | ||||||
| chr8:100029702
|
CA | C | 45 | a0000c0021t0001g0150a0001c0001t0001g0067a0001c0001t0001g0137others(42): Show | 46 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.2166+9228delT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100029702 | ||||||
| chr8:100029718
|
A | G | 1 | a0001c0001t0001g0240 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2166+9213T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100029718 | ||||||
| chr8:100029791
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2166+9140C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100029791 | ||||||
| chr8:100030074
|
A | G | 6 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0019others(3): Show | 6 | HG01257.hp1 HG01258.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.2166+8857T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100030074 | ||||||
| chr8:100030147
|
T | C | 1 | a0003c0022t0002g0110 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2166+8784A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100030147 | ||||||
| chr8:100030927
|
C | G | 1 | a0001c0001t0001g0295 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2166+8004G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100030927 | ||||||
| chr8:100030928
|
G | A | 27 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(24): Show | 27 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.2166+8003C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100030928 | ||||||
| chr8:100031009
|
T | C | 173 | a0000c0019t0001g0248a0001c0001t0001g0004a0001c0001t0001g0008others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.2166+7922A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100031009 | ||||||
| chr8:100031078
|
C | T | 2 | a0001c0001t0001g0233a0001c0001t0001g0247 | 2 | HG01255.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2166+7853G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100031078 | ||||||
| chr8:100031098
|
AT | A | 3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045 | 3 | HG00735.hp2 HG01081.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2166+7832delA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100031098 | ||||||
| chr8:100031347
|
C | T | 1 | a0010c0015t0001g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2166+7584G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100031347 | ||||||
| chr8:100031377
|
C | A | 2 | a0001c0012t0001g0112a0001c0012t0001g0131 | 2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2166+7554G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100031377 | ||||||
| chr8:100031383
|
C | T | 27 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(24): Show | 27 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.2166+7548G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100031383 | ||||||
| chr8:100031587
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2166+7344C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100031587 | ||||||
| chr8:100031590
|
C | G | 1 | a0013c0020t0001g0279 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2166+7341G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100031590 | ||||||
| chr8:100031778
|
C | T | 3 | a0001c0003t0001g0064a0001c0004t0002g0062a0001c0004t0002g0063 | 3 | HG02647.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2166+7153G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100031778 | ||||||
| chr8:100031820
|
C | T | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG02683.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2166+7111G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100031820 | ||||||
| chr8:100032121
|
A | G | 3 | a0001c0001t0001g0098a0001c0001t0001g0233a0001c0001t0001g0247 | 3 | HG01099.hp1 HG01255.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2166+6810T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100032121 | ||||||
| chr8:100032160
|
T | C | 1 | a0001c0001t0001g0260 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2166+6771A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100032160 | ||||||
| chr8:100032283
|
G | A | 1 | a0001c0003t0001g0079 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2166+6648C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100032283 | ||||||
| chr8:100032355
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2166+6576C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100032355 | ||||||
| chr8:100032410
|
G | T | 201 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.2166+6521C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100032410 | ||||||
| chr8:100032421
|
G | A | 102 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0034others(99): Show | 102 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.2166+6510C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100032421 | ||||||
| chr8:100032566
|
T | C | 58 | a0000c0019t0001g0248a0001c0001t0001g0008a0001c0001t0001g0018others(55): Show | 58 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.2166+6365A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100032566 | ||||||
| chr8:100032567
|
G | A | 2 | a0001c0004t0002g0121a0001c0004t0002g0122 | 2 | HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2166+6364C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100032567 | ||||||
| chr8:100032593
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2166+6338A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100032593 | ||||||
| chr8:100032612
|
A | G | 2 | a0001c0012t0001g0112a0001c0012t0001g0131 | 2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2166+6319T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100032612 | ||||||
| chr8:100032724
|
G | T | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2166+6207C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100032724 | ||||||
| chr8:100032751
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2166+6180C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100032751 | ||||||
| chr8:100032921
|
A | G | 27 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(24): Show | 27 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.2166+6010T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100032921 | ||||||
| chr8:100032925
|
A | C | 27 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(24): Show | 27 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.2166+6006T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100032925 | ||||||
| chr8:100033023
|
T | C | 27 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(24): Show | 27 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.2166+5908A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100033023 | ||||||
| chr8:100033419
|
A | C | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2166+5512T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100033419 | ||||||
| chr8:100033434
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2166+5497G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100033434 | ||||||
| chr8:100033444
|
T | A | 3 | a0003c0005t0001g0069a0003c0005t0001g0107a0003c0005t0001g0108 | 3 | HG02717.hp1 HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2166+5487A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100033444 | ||||||
| chr8:100033475
|
T | C | 1 | a0003c0022t0002g0110 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2166+5456A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100033475 | ||||||
| chr8:100033539
|
C | CA | 104 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0034others(101): Show | 104 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.2166+5391dupT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100033539 | ||||||
| chr8:100033557
|
C | T | 1 | a0010c0015t0001g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2166+5374G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100033557 | ||||||
| chr8:100033661
|
C | A | 3 | a0001c0001t0001g0067a0001c0001t0003g0003a0001c0003t0001g0005 | 3 | HG01243.hp2 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2166+5270G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100033661 | ||||||
| chr8:100033747
|
CA | C | 164 | a0000c0019t0001g0248a0001c0001t0001g0008a0001c0001t0001g0018others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.2166+5183delT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100033747 | ||||||
| chr8:100033755
|
T | C | 27 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(24): Show | 27 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.2166+5176A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100033755 | ||||||
| chr8:100034183
|
T | G | 1 | a0016c0025t0001g0307 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2166+4748A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100034183 | ||||||
| chr8:100034220
|
C | T | 27 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(24): Show | 27 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.2166+4711G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100034220 | ||||||
| chr8:100034221
|
A | G | 27 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(24): Show | 27 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.2166+4710T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100034221 | ||||||
| chr8:100034484
|
A | G | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2166+4447T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100034484 | ||||||
| chr8:100034599
|
G | T | 1 | a0001c0001t0001g0219 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2166+4332C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100034599 | ||||||
| chr8:100034696
|
C | T | 5 | a0001c0001t0001g0103a0001c0001t0001g0104a0006c0007t0001g0113others(2): Show | 5 | HG01884.hp2 HG02630.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2166+4235G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100034696 | ||||||
| chr8:100034905
|
T | C | 2 | a0001c0001t0001g0270a0001c0001t0001g0272 | 2 | HG00408.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.2166+4026A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100034905 | ||||||
| chr8:100034906
|
G | A | 2 | a0001c0001t0001g0270a0001c0001t0001g0272 | 2 | HG00408.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.2166+4025C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100034906 | ||||||
| chr8:100034909
|
A | G | 2 | a0001c0001t0001g0270a0001c0001t0001g0272 | 2 | HG00408.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.2166+4022T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100034909 | ||||||
| chr8:100035044
|
T | C | 1 | a0003c0005t0001g0108 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2166+3887A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100035044 | ||||||
| chr8:100035123
|
G | T | 27 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(24): Show | 27 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.2166+3808C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100035123 | ||||||
| chr8:100035220
|
C | T | 58 | a0000c0019t0001g0248a0001c0001t0001g0008a0001c0001t0001g0018others(55): Show | 58 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.2166+3711G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100035220 | ||||||
| chr8:100035380
|
G | C | 24 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(21): Show | 24 | HG00438.hp2 HG02300.hp1 NA18943.hp1 others(21): Show |
intron_variant | MODIFIER | c.2166+3551C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100035380 | ||||||
| chr8:100035793
|
T | C | 1 | a0001c0003t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2166+3138A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100035793 | ||||||
| chr8:100036091
|
G | T | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG02683.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2166+2840C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100036091 | ||||||
| chr8:100036126
|
A | AAAT | 29 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(26): Show | 29 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.2166+2804_2166+280 others(7): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100036126 | ||||||
| chr8:100036157
|
TA | T | 27 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(24): Show | 27 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.2166+2773delT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100036157 | ||||||
| chr8:100036169
|
A | C | 1 | a0004c0008t0001g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2166+2762T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100036169 | ||||||
| chr8:100036296
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2166+2635T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100036296 | ||||||
| chr8:100036546
|
T | C | 2 | a0001c0001t0001g0102a0001c0003t0001g0055 | 2 | HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2166+2385A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100036546 | ||||||
| chr8:100036553
|
C | T | 1 | a0001c0003t0001g0077 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2166+2378G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100036553 | ||||||
| chr8:100036723
|
T | C | 205 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.2166+2208A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100036723 | ||||||
| chr8:100036911
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2166+2020A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100036911 | ||||||
| chr8:100036957
|
A | C | 3 | a0001c0001t0001g0098a0001c0001t0001g0233a0001c0001t0001g0247 | 3 | HG01099.hp1 HG01255.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2166+1974T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100036957 | ||||||
| chr8:100037013
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2166+1918G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100037013 | ||||||
| chr8:100037115
|
T | C | 224 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(221): Show | 225 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.2166+1816A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100037115 | ||||||
| chr8:100037162
|
G | A | 3 | a0001c0001t0001g0284a0001c0009t0001g0100a0001c0009t0001g0101 | 3 | HG02486.hp2 HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2166+1769C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100037162 | ||||||
| chr8:100037237
|
T | C | 2 | a0001c0001t0001g0233a0001c0001t0001g0247 | 2 | HG01255.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2166+1694A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100037237 | ||||||
| chr8:100037252
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2166+1679G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100037252 | ||||||
| chr8:100037339
|
T | C | 3 | a0001c0003t0001g0074a0001c0003t0001g0075a0001c0003t0001g0076 | 3 | HG02145.hp1 HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2166+1592A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100037339 | ||||||
| chr8:100037443
|
C | T | 27 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(24): Show | 27 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.2166+1488G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100037443 | ||||||
| chr8:100037511
|
A | G | 27 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(24): Show | 27 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.2166+1420T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100037511 | ||||||
| chr8:100037668
|
T | C | 6 | a0001c0001t0001g0093a0001c0001t0001g0202a0001c0001t0001g0240others(3): Show | 6 | NA18968.hp1 NA18978.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.2166+1263A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100037668 | ||||||
| chr8:100037691
|
T | C | 2 | a0001c0009t0001g0100a0001c0009t0001g0101 | 2 | HG02486.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.2166+1240A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100037691 | ||||||
| chr8:100037708
|
A | C | 1 | a0001c0001t0001g0275 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2166+1223T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100037708 | ||||||
| chr8:100037972
|
C | G | 1 | a0001c0001t0001g0211 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2166+959G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100037972 | ||||||
| chr8:100038134
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2166+797A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100038134 | ||||||
| chr8:100038333
|
AT | A | 36 | a0000c0021t0001g0150a0001c0001t0001g0067a0001c0001t0001g0098others(33): Show | 36 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.2166+597delA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100038333 | ||||||
| chr8:100038333
|
ATT | A | 171 | a0000c0019t0001g0248a0001c0001t0001g0004a0001c0001t0001g0008others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.2166+596_2166+597d others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100038333 | ||||||
| chr8:100038418
|
T | C | 1 | a0001c0012t0001g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2166+513A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100038418 | ||||||
| chr8:100038450
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2166+481A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100038450 | ||||||
| chr8:100038474
|
C | T | 197 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.2166+457G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100038474 | ||||||
| chr8:100038521
|
C | T | 1 | a0010c0015t0001g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2166+410G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100038521 | ||||||
| chr8:100038555
|
T | C | 1 | a0001c0004t0002g0124 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2166+376A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100038555 | ||||||
| chr8:100038653
|
A | G | 1 | a0001c0009t0001g0101 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2166+278T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100038653 | ||||||
| chr8:100038712
|
G | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0103others(4): Show | 7 | HG01884.hp2 HG02630.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2166+219C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100038712 | ||||||
| chr8:100038726
|
C | T | 1 | a0010c0015t0001g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2166+205G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100038726 | ||||||
| chr8:100038768
|
T | C | 3 | a0001c0001t0001g0284a0001c0009t0001g0100a0001c0009t0001g0101 | 3 | HG02486.hp2 HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2166+163A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100038768 | ||||||
| chr8:100038796
|
C | A | 199 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.2166+135G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100038796 | ||||||
| chr8:100038839
|
C | T | 1 | a0001c0001t0001g0240 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2166+92G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100038839 | ||||||
| chr8:100038840
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2166+91C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 14/27 | chr8 | 100038840 | ||||||
| chr8:100039127
|
G | C | 1 | a0001c0012t0001g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2065-95C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 13/27 | chr8 | 100039127 | ||||||
| chr8:100039265
|
AATGGTAA others(10): Show |
A | 2 | a0001c0001t0001g0183a0001c0001t0001g0187 | 2 | HG01123.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.2065-250_2065-234d others(19): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 13/27 | chr8 | 100039265 | ||||||
| chr8:100039283
|
T | G | 2 | a0001c0001t0001g0183a0001c0001t0001g0187 | 2 | HG01123.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.2065-251A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 13/27 | chr8 | 100039283 | ||||||
| chr8:100039285
|
A | C | 2 | a0001c0001t0001g0183a0001c0001t0001g0187 | 2 | HG01123.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.2065-253T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 13/27 | chr8 | 100039285 | ||||||
| chr8:100039286
|
C | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0187 | 2 | HG01123.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.2065-254G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 13/27 | chr8 | 100039286 | ||||||
| chr8:100039288
|
G | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0187 | 2 | HG01123.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.2065-256C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 13/27 | chr8 | 100039288 | ||||||
| chr8:100039298
|
A | T | 2 | a0001c0001t0001g0067a0001c0003t0001g0005 | 2 | HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2065-266T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 13/27 | chr8 | 100039298 | ||||||
| chr8:100039348
|
C | T | 3 | a0001c0004t0002g0115a0001c0004t0002g0116a0001c0004t0005g0308 | 3 | HG00733.hp1 HG00738.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2065-316G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 13/27 | chr8 | 100039348 | ||||||
| chr8:100039370
|
G | A | 2 | a0001c0001t0001g0067a0001c0003t0001g0005 | 2 | HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2065-338C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 13/27 | chr8 | 100039370 | ||||||
| chr8:100039378
|
CT | C | 294 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(291): Show | 296 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(293): Show |
intron_variant | MODIFIER | c.2065-347delA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 13/27 | chr8 | 100039378 | ||||||
| chr8:100039385
|
T | C | 1 | a0001c0001t0001g0168 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2065-353A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 13/27 | chr8 | 100039385 | ||||||
| chr8:100039514
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2064+448A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 13/27 | chr8 | 100039514 | ||||||
| chr8:100039617
|
C | A | 1 | a0003c0005t0001g0094 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2064+345G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 13/27 | chr8 | 100039617 | ||||||
| chr8:100039636
|
G | A | 199 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.2064+326C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 13/27 | chr8 | 100039636 | ||||||
| chr8:100039666
|
G | A | 197 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.2064+296C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 13/27 | chr8 | 100039666 | ||||||
| chr8:100039720
|
A | T | 27 | a0000c0021t0001g0150a0001c0001t0001g0193a0002c0002t0001g0033others(24): Show | 27 | HG00558.hp2 HG00673.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.2064+242T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 13/27 | chr8 | 100039720 | ||||||
| chr8:100040172
|
T | C | 1 | a0010c0015t0001g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1939-85A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 12/27 | chr8 | 100040172 | ||||||
| chr8:100040346
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1939-259G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 12/27 | chr8 | 100040346 | ||||||
| chr8:100040488
|
T | A | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1939-401A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 12/27 | chr8 | 100040488 | ||||||
| chr8:100040873
|
T | C | 3 | a0002c0002t0001g0153a0002c0002t0001g0155a0002c0002t0001g0156 | 3 | HG00558.hp2 HG02040.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.1939-786A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 12/27 | chr8 | 100040873 | ||||||
| chr8:100041127
|
T | C | 302 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(299): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.1938+675A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 12/27 | chr8 | 100041127 | ||||||
| chr8:100041259
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1938+543G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 12/27 | chr8 | 100041259 | ||||||
| chr8:100041285
|
G | T | 199 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.1938+517C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 12/27 | chr8 | 100041285 | ||||||
| chr8:100041286
|
C | T | 4 | a0001c0001t0001g0067a0001c0001t0001g0134a0001c0001t0003g0003others(1): Show | 4 | HG01109.hp1 HG01243.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1938+516G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 12/27 | chr8 | 100041286 | ||||||
| chr8:100041352
|
G | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0103others(4): Show | 7 | HG01884.hp2 HG02630.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1938+450C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 12/27 | chr8 | 100041352 | ||||||
| chr8:100041364
|
G | A | 1 | a0010c0015t0001g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1938+438C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 12/27 | chr8 | 100041364 | ||||||
| chr8:100041463
|
C | T | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1938+339G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 12/27 | chr8 | 100041463 | ||||||
| chr8:100041489
|
C | CA | 179 | a0000c0019t0001g0248a0001c0001t0001g0004a0001c0001t0001g0008others(176): Show | 180 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.1938+312dupT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 12/27 | chr8 | 100041489 | ||||||
| chr8:100041489
|
C | CAA | 28 | a0000c0021t0001g0150a0001c0001t0001g0169a0001c0001t0001g0304others(25): Show | 28 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1938+311_1938+312d others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 12/27 | chr8 | 100041489 | ||||||
| chr8:100041499
|
A | AT | 5 | a0001c0001t0001g0103a0001c0001t0001g0104a0006c0007t0001g0113others(2): Show | 5 | HG01884.hp2 HG02630.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1938+302_1938+303i others(3): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 12/27 | chr8 | 100041499 | ||||||
| chr8:100041561
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1938+241G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 12/27 | chr8 | 100041561 | ||||||
| chr8:100041691
|
T | C | 2 | a0001c0012t0001g0112a0001c0012t0001g0131 | 2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1938+111A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 12/27 | chr8 | 100041691 | ||||||
| chr8:100041752
|
C | T | 199 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.1938+50G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 12/27 | chr8 | 100041752 | ||||||
| chr8:100041782
|
T | G | 1 | a0002c0002t0001g0152 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1938+20A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 12/27 | chr8 | 100041782 | ||||||
| chr8:100042060
|
C | T | 197 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1824-144G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100042060 | ||||||
| chr8:100042386
|
G | A | 2 | a0001c0001t0001g0256a0001c0001t0001g0258 | 2 | HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1824-470C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100042386 | ||||||
| chr8:100042544
|
T | C | 1 | a0010c0015t0001g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1824-628A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100042544 | ||||||
| chr8:100043011
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1824-1095G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100043011 | ||||||
| chr8:100043089
|
A | G | 197 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1824-1173T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100043089 | ||||||
| chr8:100043197
|
C | T | 1 | a0001c0001t0003g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1824-1281G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100043197 | ||||||
| chr8:100043281
|
C | T | 26 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(23): Show | 26 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.1824-1365G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100043281 | ||||||
| chr8:100043318
|
T | TC | 58 | a0000c0019t0001g0248a0001c0001t0001g0008a0001c0001t0001g0018others(55): Show | 58 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.1824-1403dupG | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100043318 | ||||||
| chr8:100043363
|
A | G | 2 | a0010c0015t0001g0117a0011c0016t0001g0132 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1824-1447T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100043363 | ||||||
| chr8:100043416
|
C | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0099 | 2 | HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1824-1500G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100043416 | ||||||
| chr8:100043505
|
G | A | 1 | a0001c0001t0001g0225 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1824-1589C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100043505 | ||||||
| chr8:100043732
|
C | T | 85 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0001g0036others(82): Show | 85 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1824-1816G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100043732 | ||||||
| chr8:100043751
|
G | A | 30 | a0000c0021t0001g0150a0001c0001t0001g0284a0001c0009t0001g0100others(27): Show | 30 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.1824-1835C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100043751 | ||||||
| chr8:100043782
|
C | A | 4 | a0001c0001t0001g0067a0001c0001t0001g0134a0001c0001t0003g0003others(1): Show | 4 | HG01109.hp1 HG01243.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1824-1866G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100043782 | ||||||
| chr8:100043804
|
A | C | 2 | a0010c0015t0001g0117a0011c0016t0001g0132 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1824-1888T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100043804 | ||||||
| chr8:100043808
|
C | A | 1 | a0001c0001t0001g0183 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1824-1892G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100043808 | ||||||
| chr8:100044082
|
T | G | 1 | a0000c0019t0001g0248 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1824-2166A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100044082 | ||||||
| chr8:100044626
|
C | CT | 91 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0008others(88): Show | 91 | HG00099.hp1 HG00558.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.1824-2711dupA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100044626 | ||||||
| chr8:100044723
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1823+2740T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100044723 | ||||||
| chr8:100044868
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1823+2595A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100044868 | ||||||
| chr8:100045053
|
G | T | 1 | a0010c0015t0001g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1823+2410C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100045053 | ||||||
| chr8:100045093
|
A | G | 2 | a0004c0008t0001g0173a0004c0008t0001g0189 | 2 | NA18970.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1823+2370T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100045093 | ||||||
| chr8:100045097
|
A | C | 200 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.1823+2366T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100045097 | ||||||
| chr8:100045113
|
CA | C | 18 | a0003c0005t0001g0002a0003c0005t0001g0057a0003c0005t0001g0059others(15): Show | 19 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.1823+2349delT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100045113 | ||||||
| chr8:100045296
|
C | G | 1 | a0001c0001t0003g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1823+2167G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100045296 | ||||||
| chr8:100045359
|
C | A | 94 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(91): Show | 94 | HG00099.hp1 HG00558.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.1823+2104G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100045359 | ||||||
| chr8:100045362
|
C | T | 1 | a0001c0009t0001g0101 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1823+2101G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100045362 | ||||||
| chr8:100045455
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1823+2008T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100045455 | ||||||
| chr8:100045593
|
T | A | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1823+1870A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100045593 | ||||||
| chr8:100045616
|
T | C | 17 | a0001c0001t0001g0036a0001c0001t0001g0178a0001c0001t0001g0182others(14): Show | 17 | HG00099.hp2 HG00733.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.1823+1847A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100045616 | ||||||
| chr8:100045708
|
A | C | 222 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.1823+1755T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100045708 | ||||||
| chr8:100045803
|
C | T | 27 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(24): Show | 27 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.1823+1660G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100045803 | ||||||
| chr8:100045817
|
A | G | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1823+1646T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100045817 | ||||||
| chr8:100046085
|
G | C | 68 | a0000c0019t0001g0248a0001c0001t0001g0004a0001c0001t0001g0008others(65): Show | 68 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.1823+1378C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100046085 | ||||||
| chr8:100046283
|
A | T | 199 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.1823+1180T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100046283 | ||||||
| chr8:100046342
|
G | A | 199 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.1823+1121C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100046342 | ||||||
| chr8:100046369
|
G | A | 222 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.1823+1094C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100046369 | ||||||
| chr8:100046465
|
G | A | 199 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.1823+998C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100046465 | ||||||
| chr8:100046715
|
A | C | 2 | a0010c0015t0001g0117a0011c0016t0001g0132 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1823+748T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100046715 | ||||||
| chr8:100046715
|
A | G | 201 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.1823+748T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100046715 | ||||||
| chr8:100046842
|
G | A | 27 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(24): Show | 27 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.1823+621C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100046842 | ||||||
| chr8:100047105
|
G | A | 2 | a0001c0001t0001g0067a0001c0003t0001g0005 | 2 | HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1823+358C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100047105 | ||||||
| chr8:100047216
|
C | A | 1 | a0001c0001t0001g0268 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1823+247G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100047216 | ||||||
| chr8:100047336
|
T | C | 2 | a0010c0015t0001g0117a0011c0016t0001g0132 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1823+127A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100047336 | ||||||
| chr8:100047404
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1823+59T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100047404 | ||||||
| chr8:100047415
|
C | T | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1823+48G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100047415 | ||||||
| chr8:100047434
|
G | A | 197 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1823+29C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 11/27 | chr8 | 100047434 | ||||||
| chr8:100047890
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1690-294C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100047890 | ||||||
| chr8:100047903
|
A | G | 4 | a0001c0001t0001g0231a0001c0001t0001g0240a0001c0001t0001g0260others(1): Show | 4 | HG00544.hp2 NA18979.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.1690-307T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100047903 | ||||||
| chr8:100047953
|
T | C | 1 | a0001c0001t0001g0219 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1690-357A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100047953 | ||||||
| chr8:100047962
|
TG | T | 222 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.1690-367delC | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100047962 | ||||||
| chr8:100047963
|
G | T | 1 | a0001c0001t0001g0224 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1690-367C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100047963 | ||||||
| chr8:100048088
|
T | C | 2 | a0001c0001t0001g0090a0001c0001t0001g0276 | 2 | NA19010.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1690-492A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100048088 | ||||||
| chr8:100048258
|
G | T | 1 | a0001c0001t0001g0237 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1690-662C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100048258 | ||||||
| chr8:100048442
|
T | C | 1 | a0001c0001t0001g0286 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1690-846A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100048442 | ||||||
| chr8:100048869
|
G | C | 1 | a0001c0001t0001g0294 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1690-1273C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100048869 | ||||||
| chr8:100048897
|
G | C | 1 | a0001c0004t0002g0127 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1690-1301C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100048897 | ||||||
| chr8:100049058
|
G | C | 1 | a0001c0001t0001g0045 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1690-1462C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100049058 | ||||||
| chr8:100049386
|
C | T | 1 | a0001c0001t0001g0236 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1690-1790G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100049386 | ||||||
| chr8:100049451
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1690-1855T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100049451 | ||||||
| chr8:100049530
|
T | C | 2 | a0001c0012t0001g0112a0001c0012t0001g0131 | 2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1690-1934A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100049530 | ||||||
| chr8:100049587
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1690-1991A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100049587 | ||||||
| chr8:100049910
|
G | C | 67 | a0000c0019t0001g0248a0001c0001t0001g0004a0001c0001t0001g0008others(64): Show | 67 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.1690-2314C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100049910 | ||||||
| chr8:100049996
|
C | T | 1 | a0002c0002t0001g0213 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1690-2400G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100049996 | ||||||
| chr8:100050036
|
C | T | 1 | a0009c0014t0001g0146 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1690-2440G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100050036 | ||||||
| chr8:100050050
|
C | CA | 196 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1690-2455dupT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100050050 | ||||||
| chr8:100050051
|
A | G | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | NA18970.hp2 NA18973.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.1690-2455T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100050051 | ||||||
| chr8:100050308
|
T | C | 3 | a0001c0001t0001g0093a0001c0001t0001g0246a0001c0001t0001g0249 | 3 | NA18968.hp1 NA19000.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1689+2494A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100050308 | ||||||
| chr8:100050316
|
A | C | 199 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.1689+2486T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100050316 | ||||||
| chr8:100050660
|
G | A | 59 | a0000c0019t0001g0248a0001c0001t0001g0008a0001c0001t0001g0018others(56): Show | 59 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.1689+2142C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100050660 | ||||||
| chr8:100050771
|
T | C | 3 | a0002c0002t0001g0083a0002c0002t0001g0084a0002c0002t0001g0085 | 3 | NA18944.hp2 NA18983.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1689+2031A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100050771 | ||||||
| chr8:100050941
|
C | T | 2 | a0010c0015t0001g0117a0011c0016t0001g0132 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1689+1861G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100050941 | ||||||
| chr8:100050961
|
T | C | 28 | a0000c0021t0001g0150a0001c0001t0001g0098a0002c0002t0001g0033others(25): Show | 28 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1689+1841A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100050961 | ||||||
| chr8:100051171
|
C | A | 1 | a0001c0001t0001g0247 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1689+1631G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051171 | ||||||
| chr8:100051213
|
C | T | 200 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.1689+1589G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051213 | ||||||
| chr8:100051395
|
T | A | 2 | a0010c0015t0001g0117a0011c0016t0001g0132 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1689+1407A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051395 | ||||||
| chr8:100051396
|
T | TATATATA others(20): Show |
2 | a0001c0001t0001g0025a0001c0001t0001g0028 | 2 | HG02300.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1689+1379_1689+140 others(31): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051396 | ||||||
| chr8:100051407
|
T | A | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1689+1395A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051407 | ||||||
| chr8:100051410
|
T | A | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1689+1392A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051410 | ||||||
| chr8:100051413
|
T | A | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1689+1389A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051413 | ||||||
| chr8:100051423
|
C | A | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1689+1379G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051423 | ||||||
| chr8:100051432
|
A | T | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1689+1370T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051432 | ||||||
| chr8:100051445
|
TTTATA | T | 4 | a0001c0001t0001g0067a0001c0001t0001g0134a0001c0001t0003g0003others(1): Show | 4 | HG01109.hp1 HG01243.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1689+1352_1689+135 others(9): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051445 | ||||||
| chr8:100051446
|
T | A | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1689+1356A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051446 | ||||||
| chr8:100051446
|
TTATA | T | 20 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0030others(17): Show | 20 | HG00099.hp1 HG01071.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.1689+1352_1689+135 others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051446 | ||||||
| chr8:100051447
|
T | C | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1689+1355A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051447 | ||||||
| chr8:100051448
|
ATAT | A | 38 | a0000c0019t0001g0248a0001c0001t0001g0018a0001c0001t0001g0019others(35): Show | 38 | HG00597.hp2 HG00673.hp1 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.1689+1351_1689+135 others(7): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051448 | ||||||
| chr8:100051451
|
T | A | 20 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0030others(17): Show | 20 | HG00099.hp1 HG01071.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.1689+1351A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051451 | ||||||
| chr8:100051455
|
A | T | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1689+1347T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051455 | ||||||
| chr8:100051459
|
T | C | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1689+1343A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051459 | ||||||
| chr8:100051462
|
A | G | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1689+1340T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051462 | ||||||
| chr8:100051481
|
A | G | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1689+1321T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051481 | ||||||
| chr8:100051488
|
T | C | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1689+1314A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051488 | ||||||
| chr8:100051492
|
A | T | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1689+1310T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051492 | ||||||
| chr8:100051498
|
A | T | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1689+1304T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051498 | ||||||
| chr8:100051508
|
TATAA | T | 196 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1689+1290_1689+129 others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051508 | ||||||
| chr8:100051511
|
A | T | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1689+1291T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051511 | ||||||
| chr8:100051512
|
A | T | 2 | a0001c0001t0001g0098a0011c0016t0001g0132 | 2 | HG01099.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1689+1290T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051512 | ||||||
| chr8:100051517
|
A | T | 27 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(24): Show | 27 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.1689+1285T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051517 | ||||||
| chr8:100051519
|
T | A | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1689+1283A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051519 | ||||||
| chr8:100051519
|
T | G | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1689+1283A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051519 | ||||||
| chr8:100051526
|
T | C | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1689+1276A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051526 | ||||||
| chr8:100051532
|
T | A | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1689+1270A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051532 | ||||||
| chr8:100051534
|
C | A | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1689+1268G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051534 | ||||||
| chr8:100051534
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1689+1268G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051534 | ||||||
| chr8:100051543
|
T | A | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1689+1259A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051543 | ||||||
| chr8:100051544
|
T | A | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1689+1258A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051544 | ||||||
| chr8:100051548
|
C | T | 2 | a0001c0001t0001g0098a0011c0016t0001g0132 | 2 | HG01099.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1689+1254G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051548 | ||||||
| chr8:100051551
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1689+1251C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051551 | ||||||
| chr8:100051554
|
T | C | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1689+1248A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051554 | ||||||
| chr8:100051555
|
T | A | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1689+1247A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051555 | ||||||
| chr8:100051555
|
T | TTATATAA others(25): Show |
1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1689+1246_1689+124 others(36): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051555 | ||||||
| chr8:100051555
|
T | TTATATAA others(25): Show |
1 | a0001c0001t0001g0297 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1689+1215_1689+124 others(36): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051555 | ||||||
| chr8:100051555
|
T | TTATATAA others(183): Show |
1 | a0010c0015t0001g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1689+1246_1689+124 others(194): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051555 | ||||||
| chr8:100051555
|
TTATATAA others(25): Show |
T | 5 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 5 | HG00609.hp2 HG00735.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.1689+1215_1689+124 others(36): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051555 | ||||||
| chr8:100051556
|
TATATAA | T | 63 | a0000c0019t0001g0248a0001c0001t0001g0004a0001c0001t0001g0008others(60): Show | 63 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.1689+1240_1689+124 others(10): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051556 | ||||||
| chr8:100051556
|
TATATAAA others(31): Show |
T | 1 | a0001c0001t0001g0104 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1689+1208_1689+124 others(42): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051556 | ||||||
| chr8:100051556
|
TATATAAA others(95): Show |
T | 1 | a0001c0003t0001g0079 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1689+1144_1689+124 others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051556 | ||||||
| chr8:100051557
|
A | T | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1689+1245T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051557 | ||||||
| chr8:100051558
|
TATAA | T | 121 | a0000c0021t0001g0150a0001c0001t0001g0022a0001c0001t0001g0029others(118): Show | 121 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1689+1240_1689+124 others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051558 | ||||||
| chr8:100051558
|
TATAAATA others(29): Show |
T | 7 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(4): Show | 7 | NA18612.hp1 NA18946.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.1689+1208_1689+124 others(40): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051558 | ||||||
| chr8:100051558
|
TATAAATA others(61): Show |
T | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | NA18955.hp2 NA19005.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1689+1176_1689+124 others(72): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051558 | ||||||
| chr8:100051559
|
A | T | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1689+1243T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051559 | ||||||
| chr8:100051562
|
A | T | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1689+1240T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051562 | ||||||
| chr8:100051567
|
A | T | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1689+1235T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051567 | ||||||
| chr8:100051571
|
T | A | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1689+1231A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051571 | ||||||
| chr8:100051571
|
TTA | T | 17 | a0000c0019t0001g0248a0003c0005t0001g0002a0003c0005t0001g0057others(14): Show | 18 | HG00673.hp1 HG02280.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.1689+1229_1689+123 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051571 | ||||||
| chr8:100051572
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1689+1230A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051572 | ||||||
| chr8:100051579
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1689+1223C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051579 | ||||||
| chr8:100051586
|
CAT | C | 13 | a0000c0021t0001g0150a0002c0002t0001g0058a0002c0002t0001g0081others(10): Show | 13 | HG00558.hp2 HG00673.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.1689+1214_1689+121 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051586 | ||||||
| chr8:100051591
|
A | G | 1 | a0002c0002t0001g0033 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1689+1211T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051591 | ||||||
| chr8:100051591
|
A | T | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1689+1211T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051591 | ||||||
| chr8:100051594
|
A | T | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1689+1208T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051594 | ||||||
| chr8:100051594
|
AATATATA others(83): Show |
A | 9 | a0001c0001t0001g0022a0001c0001t0001g0137a0001c0001t0001g0175others(6): Show | 9 | HG00621.hp1 HG01433.hp1 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.1689+1118_1689+120 others(94): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051594 | ||||||
| chr8:100051595
|
A | T | 3 | a0001c0003t0001g0064a0001c0004t0002g0062a0001c0004t0002g0063 | 3 | HG02647.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1689+1207T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051595 | ||||||
| chr8:100051596
|
T | C | 1 | a0002c0002t0001g0033 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1689+1206A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051596 | ||||||
| chr8:100051597
|
A | ACAT | 3 | a0001c0003t0001g0064a0001c0004t0002g0062a0001c0004t0002g0063 | 3 | HG02647.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1689+1204_1689+120 others(7): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051597 | ||||||
| chr8:100051600
|
TATTTATA others(105): Show |
T | 12 | a0001c0001t0001g0118a0001c0001t0001g0128a0001c0004t0002g0114others(9): Show | 12 | HG00733.hp1 HG00738.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1689+1090_1689+120 others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051600 | ||||||
| chr8:100051601
|
A | G | 1 | a0002c0002t0001g0033 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1689+1201T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051601 | ||||||
| chr8:100051601
|
ATT | A | 44 | a0000c0019t0001g0248a0001c0001t0001g0008a0001c0001t0001g0018others(41): Show | 44 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.1689+1199_1689+120 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051601 | ||||||
| chr8:100051602
|
T | TTACA | 3 | a0001c0003t0001g0064a0001c0004t0002g0062a0001c0004t0002g0063 | 3 | HG02647.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1689+1199_1689+120 others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051602 | ||||||
| chr8:100051603
|
T | A | 4 | a0001c0001t0001g0253a0001c0012t0001g0112a0001c0012t0001g0131others(1): Show | 4 | HG01943.hp2 HG02145.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1689+1199A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051603 | ||||||
| chr8:100051603
|
T | G | 1 | a0002c0002t0001g0086 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1689+1199A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051603 | ||||||
| chr8:100051603
|
TTA | T | 12 | a0002c0002t0001g0087a0002c0002t0001g0088a0002c0002t0001g0133others(9): Show | 12 | HG01081.hp1 HG02976.hp2 HG04184.hp2 others(9): Show |
intron_variant | MODIFIER | c.1689+1197_1689+119 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051603 | ||||||
| chr8:100051606
|
T | C | 1 | a0002c0002t0001g0033 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1689+1196A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051606 | ||||||
| chr8:100051608
|
T | A | 1 | a0002c0002t0001g0086 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1689+1194A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051608 | ||||||
| chr8:100051608
|
T | C | 3 | a0001c0003t0001g0064a0001c0004t0002g0062a0001c0004t0002g0063 | 3 | HG02647.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1689+1194A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051608 | ||||||
| chr8:100051610
|
T | C | 47 | a0000c0019t0001g0248a0001c0001t0001g0008a0001c0001t0001g0018others(44): Show | 47 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.1689+1192A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051610 | ||||||
| chr8:100051610
|
T | TAC | 78 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0001g0036others(75): Show | 78 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1689+1191_1689+119 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051610 | ||||||
| chr8:100051611
|
G | A | 4 | a0001c0003t0001g0064a0001c0004t0002g0062a0001c0004t0002g0063others(1): Show | 4 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1689+1191C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051611 | ||||||
| chr8:100051612
|
TTTATACA others(93): Show |
T | 45 | a0000c0019t0001g0248a0001c0001t0001g0008a0001c0001t0001g0018others(42): Show | 45 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.1689+1090_1689+118 others(104): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051612 | ||||||
| chr8:100051613
|
T | A | 116 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0029others(113): Show | 116 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.1689+1189A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051613 | ||||||
| chr8:100051616
|
T | A | 33 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0099others(30): Show | 33 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.1689+1186A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051616 | ||||||
| chr8:100051618
|
C | A | 1 | a0002c0002t0001g0086 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1689+1184G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051618 | ||||||
| chr8:100051618
|
C | CGT | 65 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0048others(62): Show | 65 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.1689+1183_1689+118 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051618 | ||||||
| chr8:100051619
|
A | AT | 3 | a0001c0003t0001g0064a0001c0004t0002g0062a0001c0004t0002g0063 | 3 | HG02647.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1689+1182dupA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051619 | ||||||
| chr8:100051619
|
A | G | 17 | a0001c0001t0001g0029a0001c0001t0001g0097a0001c0001t0001g0135others(14): Show | 17 | HG01074.hp1 HG01261.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1689+1183T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051619 | ||||||
| chr8:100051620
|
T | A | 1 | a0002c0002t0001g0086 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1689+1182A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051620 | ||||||
| chr8:100051621
|
ATATAAAT others(39): Show |
A | 14 | a0001c0001t0001g0029a0001c0001t0001g0097a0001c0001t0001g0135others(11): Show | 14 | HG01074.hp1 HG01261.hp2 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.1689+1135_1689+118 others(50): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051621 | ||||||
| chr8:100051622
|
T | C | 3 | a0001c0003t0001g0064a0001c0004t0002g0062a0001c0004t0002g0063 | 3 | HG02647.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1689+1180A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051622 | ||||||
| chr8:100051626
|
A | C | 67 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0048others(64): Show | 67 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1689+1176T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051626 | ||||||
| chr8:100051626
|
A | T | 6 | a0001c0001t0003g0003a0001c0003t0001g0064a0001c0004t0002g0062others(3): Show | 6 | HG01243.hp2 HG02145.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1689+1176T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051626 | ||||||
| chr8:100051627
|
A | G | 67 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0048others(64): Show | 67 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1689+1175T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051627 | ||||||
| chr8:100051628
|
T | C | 1 | a0001c0012t0001g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1689+1174A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051628 | ||||||
| chr8:100051629
|
A | G | 1 | a0001c0012t0001g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1689+1173T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051629 | ||||||
| chr8:100051629
|
A | T | 1 | a0001c0001t0003g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1689+1173T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051629 | ||||||
| chr8:100051631
|
A | T | 1 | a0002c0002t0001g0086 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1689+1171T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051631 | ||||||
| chr8:100051631
|
ATATTTAT others(7): Show |
A | 2 | a0001c0001t0001g0256a0001c0001t0001g0258 | 2 | HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1689+1157_1689+117 others(18): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051631 | ||||||
| chr8:100051634
|
T | C | 68 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0048others(65): Show | 68 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.1689+1168A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051634 | ||||||
| chr8:100051635
|
T | A | 21 | a0000c0021t0001g0150a0001c0001t0003g0003a0001c0003t0001g0064others(18): Show | 21 | HG00558.hp2 HG00673.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.1689+1167A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051635 | ||||||
| chr8:100051635
|
T | G | 65 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0048others(62): Show | 65 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.1689+1167A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051635 | ||||||
| chr8:100051636
|
T | C | 1 | a0001c0012t0001g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1689+1166A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051636 | ||||||
| chr8:100051636
|
T | TAAATACA others(7): Show |
1 | a0002c0002t0001g0096 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1689+1165_1689+116 others(18): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051636 | ||||||
| chr8:100051637
|
A | G | 1 | a0001c0012t0001g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1689+1165T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051637 | ||||||
| chr8:100051638
|
T | A | 14 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(11): Show | 14 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1689+1164A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051638 | ||||||
| chr8:100051639
|
ATATGTTT others(31): Show |
A | 63 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0049others(60): Show | 63 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.1689+1125_1689+116 others(42): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051639 | ||||||
| chr8:100051642
|
T | C | 14 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(11): Show | 14 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1689+1160A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051642 | ||||||
| chr8:100051642
|
T | TAC | 7 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(4): Show | 7 | NA18612.hp1 NA18946.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.1689+1159_1689+116 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051642 | ||||||
| chr8:100051643
|
G | A | 19 | a0000c0021t0001g0150a0001c0001t0001g0036a0001c0001t0003g0003others(16): Show | 19 | HG00558.hp2 HG00673.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1689+1159C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051643 | ||||||
| chr8:100051644
|
T | C | 2 | a0001c0001t0001g0036a0001c0012t0001g0131 | 2 | HG02738.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1689+1158A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051644 | ||||||
| chr8:100051645
|
T | A | 14 | a0001c0001t0001g0098a0001c0001t0001g0104a0001c0001t0001g0168others(11): Show | 14 | HG01099.hp1 HG01243.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.1689+1157A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051645 | ||||||
| chr8:100051645
|
T | G | 17 | a0000c0021t0001g0150a0001c0001t0001g0036a0001c0012t0001g0131others(14): Show | 17 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.1689+1157A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051645 | ||||||
| chr8:100051646
|
T | A | 3 | a0001c0001t0003g0003a0005c0006t0001g0082a0005c0006t0001g0092 | 3 | HG01081.hp1 HG01243.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.1689+1156A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051646 | ||||||
| chr8:100051648
|
T | A | 2 | a0001c0001t0001g0098a0001c0001t0001g0104 | 2 | HG01099.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1689+1154A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051648 | ||||||
| chr8:100051650
|
C | A | 16 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(13): Show | 16 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.1689+1152G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051650 | ||||||
| chr8:100051650
|
C | T | 3 | a0001c0001t0001g0036a0001c0001t0003g0003a0001c0012t0001g0131 | 3 | HG01243.hp2 HG02738.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1689+1152G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051650 | ||||||
| chr8:100051650
|
CAT | C | 8 | a0002c0002t0001g0087a0002c0002t0001g0088a0002c0002t0001g0133others(5): Show | 8 | HG04184.hp2 NA18747.hp2 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1689+1150_1689+115 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051650 | ||||||
| chr8:100051651
|
A | G | 10 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(7): Show | 10 | HG02145.hp2 HG02630.hp2 HG03579.hp1 others(7): Show |
intron_variant | MODIFIER | c.1689+1151T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051651 | ||||||
| chr8:100051652
|
TATATAAA others(23): Show |
T | 1 | a0003c0005t0001g0059 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1689+1120_1689+114 others(34): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051652 | ||||||
| chr8:100051653
|
A | G | 2 | a0005c0006t0001g0082a0005c0006t0001g0092 | 2 | HG01081.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1689+1149T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051653 | ||||||
| chr8:100051654
|
T | C | 2 | a0001c0001t0001g0036a0001c0012t0001g0131 | 2 | HG02738.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1689+1148A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051654 | ||||||
| chr8:100051655
|
A | G | 2 | a0001c0001t0001g0036a0001c0012t0001g0131 | 2 | HG02738.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1689+1147T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051655 | ||||||
| chr8:100051655
|
A | T | 1 | a0001c0001t0003g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1689+1147T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051655 | ||||||
| chr8:100051656
|
TAA | T | 21 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(18): Show | 22 | HG02486.hp1 HG02559.hp2 HG02717.hp1 others(19): Show |
intron_variant | MODIFIER | c.1689+1144_1689+114 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051656 | ||||||
| chr8:100051658
|
A | C | 3 | a0001c0001t0001g0256a0001c0001t0001g0258a0001c0012t0001g0112 | 3 | HG02145.hp2 HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1689+1144T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051658 | ||||||
| chr8:100051658
|
A | T | 20 | a0000c0021t0001g0150a0001c0001t0001g0036a0001c0001t0003g0003others(17): Show | 20 | HG00558.hp2 HG00673.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.1689+1144T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051658 | ||||||
| chr8:100051658
|
AATATATA others(19): Show |
A | 6 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0103others(3): Show | 6 | HG01884.hp2 HG02630.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1689+1118_1689+114 others(30): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051658 | ||||||
| chr8:100051659
|
A | G | 17 | a0000c0021t0001g0150a0001c0001t0001g0256a0001c0001t0001g0258others(14): Show | 17 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.1689+1143T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051659 | ||||||
| chr8:100051660
|
T | C | 3 | a0001c0003t0001g0064a0001c0004t0002g0062a0001c0004t0002g0063 | 3 | HG02647.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1689+1142A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051660 | ||||||
| chr8:100051662
|
T | C | 7 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(4): Show | 7 | NA18612.hp1 NA18946.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.1689+1140A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051662 | ||||||
| chr8:100051663
|
A | G | 7 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(4): Show | 7 | NA18612.hp1 NA18946.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.1689+1139T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051663 | ||||||
| chr8:100051663
|
A | T | 1 | a0001c0001t0003g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1689+1139T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051663 | ||||||
| chr8:100051663
|
AT | A | 3 | a0001c0003t0001g0064a0001c0004t0002g0062a0001c0004t0002g0063 | 3 | HG02647.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1689+1138delA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051663 | ||||||
| chr8:100051664
|
T | A | 14 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(11): Show | 14 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1689+1138A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051664 | ||||||
| chr8:100051664
|
T | C | 2 | a0001c0001t0001g0036a0001c0012t0001g0131 | 2 | HG02738.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1689+1138A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051664 | ||||||
| chr8:100051665
|
A | G | 2 | a0001c0001t0001g0036a0001c0012t0001g0131 | 2 | HG02738.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1689+1137T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051665 | ||||||
| chr8:100051665
|
A | T | 15 | a0003c0005t0001g0002a0003c0005t0001g0057a0003c0005t0001g0060others(12): Show | 16 | HG02451.hp2 HG02486.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.1689+1137T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051665 | ||||||
| chr8:100051667
|
T | A | 42 | a0000c0021t0001g0150a0001c0001t0001g0036a0001c0001t0001g0168others(39): Show | 43 | HG00558.hp2 HG00673.hp2 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.1689+1135A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051667 | ||||||
| chr8:100051667
|
T | G | 5 | a0001c0003t0001g0064a0001c0004t0002g0062a0001c0004t0002g0063others(2): Show | 5 | HG01081.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1689+1135A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051667 | ||||||
| chr8:100051668
|
T | C | 3 | a0001c0001t0001g0256a0001c0001t0001g0258a0001c0012t0001g0112 | 3 | HG02145.hp2 HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1689+1134A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051668 | ||||||
| chr8:100051669
|
A | G | 3 | a0001c0001t0001g0256a0001c0001t0001g0258a0001c0012t0001g0112 | 3 | HG02145.hp2 HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1689+1133T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051669 | ||||||
| chr8:100051672
|
T | A | 15 | a0000c0021t0001g0150a0001c0001t0003g0003a0002c0002t0001g0033others(12): Show | 15 | HG00558.hp2 HG00673.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1689+1130A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051672 | ||||||
| chr8:100051672
|
T | C | 8 | a0001c0001t0001g0036a0001c0001t0001g0168a0001c0001t0001g0169others(5): Show | 8 | HG02738.hp2 NA18612.hp1 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.1689+1130A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051672 | ||||||
| chr8:100051673
|
A | G | 8 | a0001c0001t0001g0036a0001c0001t0001g0168a0001c0001t0001g0169others(5): Show | 8 | HG02738.hp2 NA18612.hp1 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.1689+1129T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051673 | ||||||
| chr8:100051673
|
ATGTT | A | 3 | a0001c0001t0001g0256a0001c0001t0001g0258a0001c0012t0001g0112 | 3 | HG02145.hp2 HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1689+1125_1689+112 others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051673 | ||||||
| chr8:100051674
|
T | A | 14 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(11): Show | 14 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1689+1128A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051674 | ||||||
| chr8:100051674
|
T | C | 30 | a0001c0001t0001g0029a0001c0001t0001g0097a0001c0001t0001g0135others(27): Show | 31 | HG01074.hp1 HG01261.hp2 HG02300.hp2 others(28): Show |
intron_variant | MODIFIER | c.1689+1128A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051674 | ||||||
| chr8:100051674
|
T | TAC | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | NA18955.hp2 NA19005.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1689+1127_1689+112 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051674 | ||||||
| chr8:100051675
|
G | A | 29 | a0000c0021t0001g0150a0001c0001t0001g0036a0001c0001t0001g0168others(26): Show | 29 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.1689+1127C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051675 | ||||||
| chr8:100051676
|
T | A | 15 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(12): Show | 15 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.1689+1126A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051676 | ||||||
| chr8:100051676
|
T | C | 1 | a0001c0001t0001g0104 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1689+1126A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051676 | ||||||
| chr8:100051677
|
T | A | 68 | a0000c0021t0001g0150a0001c0001t0001g0029a0001c0001t0001g0036others(65): Show | 69 | HG00558.hp2 HG00673.hp2 HG01074.hp1 others(66): Show |
intron_variant | MODIFIER | c.1689+1125A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051677 | ||||||
| chr8:100051678
|
T | A | 2 | a0005c0006t0001g0082a0005c0006t0001g0092 | 2 | HG01081.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1689+1124A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051678 | ||||||
| chr8:100051680
|
T | A | 10 | a0002c0002t0001g0087a0002c0002t0001g0088a0002c0002t0001g0133others(7): Show | 10 | HG01081.hp1 HG04184.hp2 NA18747.hp2 others(7): Show |
intron_variant | MODIFIER | c.1689+1122A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051680 | ||||||
| chr8:100051682
|
C | A | 3 | a0002c0002t0001g0086a0005c0006t0001g0082a0005c0006t0001g0092 | 3 | HG01081.hp1 NA18965.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1689+1120G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051682 | ||||||
| chr8:100051682
|
C | T | 32 | a0000c0021t0001g0150a0001c0001t0001g0104a0001c0001t0003g0003others(29): Show | 33 | HG00558.hp2 HG00673.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.1689+1120G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051682 | ||||||
| chr8:100051683
|
A | G | 91 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0001g0036others(88): Show | 91 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1689+1119T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051683 | ||||||
| chr8:100051683
|
ATATATAT others(3): Show |
A | 7 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(4): Show | 7 | NA18955.hp1 NA18970.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.1689+1109_1689+111 others(14): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051683 | ||||||
| chr8:100051684
|
T | A | 16 | a0001c0001t0001g0104a0003c0005t0001g0002a0003c0005t0001g0057others(13): Show | 17 | HG02451.hp2 HG02486.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.1689+1118A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051684 | ||||||
| chr8:100051684
|
T | C | 1 | a0002c0002t0001g0289 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1689+1118A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051684 | ||||||
| chr8:100051684
|
T | TATATAA | 3 | a0001c0001t0001g0098a0010c0015t0001g0117a0011c0016t0001g0132 | 3 | HG01099.hp1 HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1689+1117_1689+111 others(10): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051684 | ||||||
| chr8:100051685
|
A | ATTTAT | 14 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(11): Show | 14 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1689+1116_1689+111 others(9): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051685 | ||||||
| chr8:100051685
|
A | G | 1 | a0002c0002t0001g0289 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1689+1117T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051685 | ||||||
| chr8:100051686
|
T | A | 1 | a0002c0002t0001g0086 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1689+1116A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051686 | ||||||
| chr8:100051687
|
A | ACAT | 3 | a0001c0003t0001g0064a0001c0004t0002g0062a0001c0004t0002g0063 | 3 | HG02647.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1689+1114_1689+111 others(7): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051687 | ||||||
| chr8:100051687
|
A | T | 1 | a0001c0001t0003g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1689+1115T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051687 | ||||||
| chr8:100051690
|
T | A | 9 | a0001c0003t0001g0079a0002c0002t0001g0087a0002c0002t0001g0088others(6): Show | 9 | HG04184.hp2 NA18612.hp2 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.1689+1112A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051690 | ||||||
| chr8:100051690
|
T | C | 1 | a0001c0012t0001g0131 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1689+1112A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051690 | ||||||
| chr8:100051691
|
A | G | 1 | a0001c0012t0001g0131 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1689+1111T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051691 | ||||||
| chr8:100051691
|
AT | A | 14 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(11): Show | 14 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1689+1110delA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051691 | ||||||
| chr8:100051691
|
ATT | A | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | NA18955.hp2 NA19005.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1689+1109_1689+111 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051691 | ||||||
| chr8:100051692
|
T | C | 92 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0001g0036others(89): Show | 92 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.1689+1110A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051692 | ||||||
| chr8:100051693
|
T | A | 15 | a0001c0001t0003g0003a0001c0003t0001g0064a0001c0003t0001g0079others(12): Show | 15 | HG01243.hp2 HG02647.hp1 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.1689+1109A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051693 | ||||||
| chr8:100051693
|
T | G | 89 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0001g0036others(86): Show | 89 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1689+1109A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051693 | ||||||
| chr8:100051694
|
T | A | 1 | a0002c0002t0001g0086 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1689+1108A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051694 | ||||||
| chr8:100051694
|
T | C | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | NA18955.hp2 NA19005.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1689+1108A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051694 | ||||||
| chr8:100051695
|
A | ATATATGT others(17): Show |
1 | a0001c0003t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1689+1106_1689+110 others(28): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051695 | ||||||
| chr8:100051695
|
A | G | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | NA18955.hp2 NA19005.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1689+1107T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051695 | ||||||
| chr8:100051696
|
T | A | 1 | a0001c0001t0003g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1689+1106A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051696 | ||||||
| chr8:100051700
|
TAC | T | 17 | a0001c0001t0001g0067a0001c0001t0001g0134a0003c0005t0001g0002others(14): Show | 18 | HG01109.hp1 HG02451.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.1689+1100_1689+110 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051700 | ||||||
| chr8:100051702
|
C | A | 27 | a0000c0021t0001g0150a0001c0003t0001g0064a0001c0004t0002g0062others(24): Show | 27 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(24): Show |
intron_variant | MODIFIER | c.1689+1100G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051702 | ||||||
| chr8:100051702
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1689+1100G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051702 | ||||||
| chr8:100051703
|
G | A | 24 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(21): Show | 24 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(21): Show |
intron_variant | MODIFIER | c.1689+1099C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051703 | ||||||
| chr8:100051703
|
G | T | 20 | a0001c0003t0001g0064a0001c0004t0002g0062a0001c0004t0002g0063others(17): Show | 21 | HG01081.hp1 HG02451.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.1689+1099C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051703 | ||||||
| chr8:100051703
|
GTA | G | 4 | a0001c0001t0001g0022a0001c0001t0001g0177a0001c0001t0001g0181others(1): Show | 4 | HG00621.hp1 HG02004.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.1689+1097_1689+109 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051703 | ||||||
| chr8:100051703
|
GTATATAT others(3): Show |
G | 2 | a0001c0001t0001g0098a0001c0001t0001g0184 | 2 | HG01099.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1689+1089_1689+109 others(14): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051703 | ||||||
| chr8:100051704
|
T | TAC | 7 | a0002c0002t0001g0087a0002c0002t0001g0133a0002c0002t0001g0151others(4): Show | 7 | HG04184.hp2 NA18747.hp2 NA18991.hp1 others(4): Show |
intron_variant | MODIFIER | c.1689+1097_1689+109 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051704 | ||||||
| chr8:100051704
|
T | TACATGTA others(122): Show |
1 | a0002c0002t0001g0088 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1689+1097_1689+109 others(133): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051704 | ||||||
| chr8:100051704
|
TATATATA others(1): Show |
T | 11 | a0001c0001t0001g0004a0001c0001t0001g0029a0001c0001t0001g0099others(8): Show | 11 | HG01884.hp2 HG02630.hp1 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.1689+1090_1689+109 others(12): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051704 | ||||||
| chr8:100051705
|
A | T | 3 | a0001c0001t0001g0067a0001c0001t0001g0134a0001c0003t0001g0005 | 3 | HG01109.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1689+1097T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051705 | ||||||
| chr8:100051706
|
T | C | 3 | a0001c0003t0001g0064a0001c0004t0002g0062a0001c0004t0002g0063 | 3 | HG02647.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1689+1096A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051706 | ||||||
| chr8:100051707
|
A | AT | 3 | a0001c0003t0001g0064a0001c0004t0002g0062a0001c0004t0002g0063 | 3 | HG02647.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1689+1094dupA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051707 | ||||||
| chr8:100051707
|
A | G | 7 | a0002c0002t0001g0087a0002c0002t0001g0133a0002c0002t0001g0151others(4): Show | 7 | HG04184.hp2 NA18747.hp2 NA18991.hp1 others(4): Show |
intron_variant | MODIFIER | c.1689+1095T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051707 | ||||||
| chr8:100051707
|
A | T | 1 | a0001c0001t0003g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1689+1095T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051707 | ||||||
| chr8:100051708
|
T | A | 1 | a0002c0002t0001g0096 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1689+1094A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051708 | ||||||
| chr8:100051710
|
T | C | 5 | a0001c0001t0001g0067a0001c0001t0001g0134a0001c0003t0001g0005others(2): Show | 5 | HG01109.hp1 HG02976.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1689+1092A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051710 | ||||||
| chr8:100051710
|
TA | T | 14 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(11): Show | 14 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1689+1091delT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051710 | ||||||
| chr8:100051711
|
A | ACG | 88 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0048others(85): Show | 88 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.1689+1090_1689+109 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051711 | ||||||
| chr8:100051711
|
A | G | 1 | a0002c0002t0001g0289 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1689+1091T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051711 | ||||||
| chr8:100051712
|
A | C | 11 | a0001c0001t0001g0022a0001c0001t0001g0137a0001c0001t0001g0175others(8): Show | 11 | HG00621.hp1 HG02004.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.1689+1090T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051712 | ||||||
| chr8:100051712
|
A | T | 96 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0048others(93): Show | 96 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.1689+1090T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051712 | ||||||
| chr8:100051712
|
AATAT | A | 15 | a0003c0005t0001g0002a0003c0005t0001g0057a0003c0005t0001g0060others(12): Show | 16 | HG02451.hp2 HG02486.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.1689+1086_1689+108 others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051712 | ||||||
| chr8:100051713
|
A | G | 9 | a0001c0001t0001g0022a0001c0001t0001g0137a0001c0001t0001g0175others(6): Show | 9 | HG00621.hp1 HG02004.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.1689+1089T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051713 | ||||||
| chr8:100051716
|
T | A | 2 | a0001c0001t0003g0003a0010c0015t0001g0117 | 2 | HG01243.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1689+1086A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051716 | ||||||
| chr8:100051719
|
A | G | 17 | a0001c0001t0003g0003a0003c0005t0001g0002a0003c0005t0001g0057others(14): Show | 18 | HG01243.hp2 HG02451.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.1689+1083T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051719 | ||||||
| chr8:100051720
|
T | A | 3 | a0001c0003t0001g0064a0001c0004t0002g0062a0001c0004t0002g0063 | 3 | HG02647.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1689+1082A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051720 | ||||||
| chr8:100051720
|
T | C | 162 | a0000c0019t0001g0248a0001c0001t0001g0004a0001c0001t0001g0008others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.1689+1082A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051720 | ||||||
| chr8:100051720
|
T | TGTATAAA others(24): Show |
1 | a0005c0006t0001g0091 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1689+1081_1689+108 others(35): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051720 | ||||||
| chr8:100051721
|
T | A | 11 | a0001c0001t0001g0022a0001c0001t0001g0137a0001c0001t0001g0175others(8): Show | 11 | HG00621.hp1 HG02004.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.1689+1081A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051721 | ||||||
| chr8:100051721
|
T | G | 166 | a0000c0019t0001g0248a0001c0001t0001g0004a0001c0001t0001g0008others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.1689+1081A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051721 | ||||||
| chr8:100051722
|
T | A | 2 | a0005c0006t0001g0082a0005c0006t0001g0092 | 2 | HG01081.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1689+1080A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051722 | ||||||
| chr8:100051722
|
T | C | 4 | a0001c0001t0001g0022a0001c0001t0001g0177a0001c0001t0001g0181others(1): Show | 4 | HG00621.hp1 HG02004.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.1689+1080A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051722 | ||||||
| chr8:100051723
|
A | ACG | 3 | a0001c0001t0001g0137a0001c0001t0001g0175a0011c0016t0001g0132 | 3 | HG02056.hp2 HG03225.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1689+1078_1689+107 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051723 | ||||||
| chr8:100051723
|
A | G | 4 | a0001c0001t0001g0022a0001c0001t0001g0177a0001c0001t0001g0181others(1): Show | 4 | HG00621.hp1 HG02004.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.1689+1079T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051723 | ||||||
| chr8:100051724
|
T | C | 3 | a0001c0003t0001g0064a0001c0004t0002g0062a0001c0004t0002g0063 | 3 | HG02647.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1689+1078A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051724 | ||||||
| chr8:100051726
|
T | A | 7 | a0002c0002t0001g0087a0002c0002t0001g0096a0002c0002t0001g0133others(4): Show | 7 | HG04184.hp2 NA18747.hp2 NA18991.hp1 others(4): Show |
intron_variant | MODIFIER | c.1689+1076A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051726 | ||||||
| chr8:100051726
|
TA | T | 3 | a0001c0003t0001g0064a0001c0004t0002g0062a0001c0004t0002g0063 | 3 | HG02647.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1689+1075delT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051726 | ||||||
| chr8:100051728
|
TAC | T | 4 | a0001c0001t0001g0284a0001c0009t0001g0100a0001c0009t0001g0101others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1689+1072_1689+107 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051728 | ||||||
| chr8:100051729
|
AC | A | 14 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(11): Show | 14 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1689+1072delG | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051729 | ||||||
| chr8:100051730
|
C | T | 29 | a0001c0001t0003g0003a0001c0003t0001g0064a0001c0004t0002g0062others(26): Show | 30 | HG01081.hp1 HG01243.hp2 HG02451.hp2 others(27): Show |
intron_variant | MODIFIER | c.1689+1072G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051730 | ||||||
| chr8:100051731
|
G | A | 24 | a0000c0021t0001g0150a0001c0003t0001g0064a0001c0004t0002g0062others(21): Show | 24 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(21): Show |
intron_variant | MODIFIER | c.1689+1071C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051731 | ||||||
| chr8:100051731
|
G | T | 23 | a0001c0001t0001g0284a0001c0001t0003g0003a0001c0009t0001g0100others(20): Show | 24 | HG01081.hp1 HG01243.hp2 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.1689+1071C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051731 | ||||||
| chr8:100051732
|
T | A | 3 | a0001c0003t0001g0064a0001c0004t0002g0062a0001c0004t0002g0063 | 3 | HG02647.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1689+1070A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051732 | ||||||
| chr8:100051732
|
T | C | 1 | a0002c0002t0001g0096 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1689+1070A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051732 | ||||||
| chr8:100051734
|
T | A | 6 | a0002c0002t0001g0087a0002c0002t0001g0133a0002c0002t0001g0151others(3): Show | 6 | HG04184.hp2 NA18747.hp2 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.1689+1068A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051734 | ||||||
| chr8:100051734
|
T | TA | 14 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(11): Show | 14 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1689+1067dupT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051734 | ||||||
| chr8:100051736
|
T | A | 6 | a0002c0002t0001g0087a0002c0002t0001g0133a0002c0002t0001g0151others(3): Show | 6 | HG04184.hp2 NA18747.hp2 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.1689+1066A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051736 | ||||||
| chr8:100051738
|
T | A | 6 | a0002c0002t0001g0087a0002c0002t0001g0133a0002c0002t0001g0151others(3): Show | 6 | HG04184.hp2 NA18747.hp2 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.1689+1064A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051738 | ||||||
| chr8:100051738
|
T | C | 2 | a0002c0002t0001g0086a0002c0002t0001g0088 | 2 | NA18946.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1689+1064A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051738 | ||||||
| chr8:100051739
|
A | G | 2 | a0002c0002t0001g0086a0002c0002t0001g0088 | 2 | NA18946.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1689+1063T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051739 | ||||||
| chr8:100051740
|
A | C | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG02683.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1689+1062T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051740 | ||||||
| chr8:100051740
|
A | T | 8 | a0002c0002t0001g0086a0002c0002t0001g0087a0002c0002t0001g0088others(5): Show | 8 | HG04184.hp2 NA18747.hp2 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1689+1062T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051740 | ||||||
| chr8:100051741
|
A | G | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG02683.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1689+1061T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051741 | ||||||
| chr8:100051741
|
ATATATAT others(1): Show |
A | 15 | a0003c0005t0001g0002a0003c0005t0001g0057a0003c0005t0001g0060others(12): Show | 16 | HG02451.hp2 HG02486.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.1689+1053_1689+106 others(12): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051741 | ||||||
| chr8:100051743
|
A | G | 3 | a0001c0009t0001g0100a0001c0009t0001g0101a0003c0005t0001g0059 | 3 | HG02280.hp1 HG02486.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1689+1059T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051743 | ||||||
| chr8:100051744
|
T | A | 14 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(11): Show | 14 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1689+1058A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051744 | ||||||
| chr8:100051745
|
A | T | 3 | a0001c0009t0001g0100a0001c0009t0001g0101a0003c0005t0001g0059 | 3 | HG02280.hp1 HG02486.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1689+1057T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051745 | ||||||
| chr8:100051746
|
T | A | 2 | a0005c0006t0001g0082a0005c0006t0001g0092 | 2 | HG01081.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1689+1056A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051746 | ||||||
| chr8:100051747
|
ATT | A | 3 | a0001c0009t0001g0100a0001c0009t0001g0101a0003c0005t0001g0059 | 3 | HG02280.hp1 HG02486.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1689+1053_1689+105 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051747 | ||||||
| chr8:100051748
|
T | C | 2 | a0002c0002t0001g0086a0002c0002t0001g0088 | 2 | NA18946.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1689+1054A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051748 | ||||||
| chr8:100051749
|
T | A | 17 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(14): Show | 17 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.1689+1053A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051749 | ||||||
| chr8:100051749
|
T | G | 2 | a0002c0002t0001g0086a0002c0002t0001g0088 | 2 | NA18946.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1689+1053A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051749 | ||||||
| chr8:100051749
|
T | TTATATAT others(3): Show |
2 | a0001c0001t0001g0284a0010c0015t0001g0117 | 2 | HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1689+1052_1689+105 others(14): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051749 | ||||||
| chr8:100051749
|
T | TTATATAT others(35): Show |
1 | a0001c0001t0001g0271 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1689+1011_1689+105 others(46): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051749 | ||||||
| chr8:100051750
|
T | A | 2 | a0005c0006t0001g0082a0005c0006t0001g0092 | 2 | HG01081.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1689+1052A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051750 | ||||||
| chr8:100051751
|
A | AT | 6 | a0002c0002t0001g0087a0002c0002t0001g0133a0002c0002t0001g0151others(3): Show | 6 | HG04184.hp2 NA18747.hp2 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.1689+1050dupA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051751 | ||||||
| chr8:100051752
|
T | A | 14 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(11): Show | 14 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1689+1050A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051752 | ||||||
| chr8:100051756
|
T | C | 2 | a0002c0002t0001g0086a0002c0002t0001g0088 | 2 | NA18946.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1689+1046A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051756 | ||||||
| chr8:100051756
|
T | TA | 6 | a0002c0002t0001g0087a0002c0002t0001g0133a0002c0002t0001g0151others(3): Show | 6 | HG04184.hp2 NA18747.hp2 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.1689+1045_1689+104 others(5): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051756 | ||||||
| chr8:100051757
|
T | A | 17 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(14): Show | 17 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.1689+1045A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051757 | ||||||
| chr8:100051757
|
T | G | 2 | a0002c0002t0001g0086a0002c0002t0001g0088 | 2 | NA18946.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1689+1045A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051757 | ||||||
| chr8:100051758
|
T | A | 2 | a0005c0006t0001g0082a0005c0006t0001g0092 | 2 | HG01081.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1689+1044A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051758 | ||||||
| chr8:100051758
|
T | C | 1 | a0002c0002t0001g0096 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1689+1044A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051758 | ||||||
| chr8:100051759
|
A | G | 1 | a0002c0002t0001g0096 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1689+1043T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051759 | ||||||
| chr8:100051760
|
T | A | 14 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(11): Show | 14 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1689+1042A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051760 | ||||||
| chr8:100051766
|
A | C | 17 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(14): Show | 17 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.1689+1036T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051766 | ||||||
| chr8:100051767
|
A | G | 3 | a0002c0002t0001g0086a0002c0002t0001g0088a0002c0002t0001g0096 | 3 | NA18946.hp2 NA18965.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1689+1035T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051767 | ||||||
| chr8:100051769
|
G | A | 28 | a0000c0021t0001g0150a0001c0009t0001g0100a0001c0009t0001g0101others(25): Show | 28 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1689+1033C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051769 | ||||||
| chr8:100051770
|
T | A | 1 | a0005c0006t0001g0091 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1689+1032A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051770 | ||||||
| chr8:100051770
|
T | TATA | 6 | a0002c0002t0001g0087a0002c0002t0001g0133a0002c0002t0001g0151others(3): Show | 6 | HG04184.hp2 NA18747.hp2 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.1689+1031_1689+103 others(7): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051770 | ||||||
| chr8:100051771
|
T | A | 22 | a0000c0021t0001g0150a0001c0009t0001g0100a0001c0009t0001g0101others(19): Show | 22 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.1689+1031A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051771 | ||||||
| chr8:100051772
|
T | A | 6 | a0002c0002t0001g0087a0002c0002t0001g0133a0002c0002t0001g0151others(3): Show | 6 | HG04184.hp2 NA18747.hp2 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.1689+1030A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051772 | ||||||
| chr8:100051772
|
T | C | 2 | a0005c0006t0001g0082a0005c0006t0001g0092 | 2 | HG01081.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1689+1030A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051772 | ||||||
| chr8:100051772
|
T | TAA | 14 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(11): Show | 14 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1689+1029_1689+103 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051772 | ||||||
| chr8:100051773
|
A | ATACG | 3 | a0002c0002t0001g0086a0002c0002t0001g0088a0002c0002t0001g0096 | 3 | NA18946.hp2 NA18965.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1689+1028_1689+102 others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051773 | ||||||
| chr8:100051774
|
T | A | 1 | a0005c0006t0001g0091 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1689+1028A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051774 | ||||||
| chr8:100051775
|
A | T | 2 | a0001c0009t0001g0100a0001c0009t0001g0101 | 2 | HG02486.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1689+1027T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051775 | ||||||
| chr8:100051779
|
A | T | 1 | a0003c0005t0001g0059 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1689+1023T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051779 | ||||||
| chr8:100051780
|
T | A | 2 | a0005c0006t0001g0082a0005c0006t0001g0092 | 2 | HG01081.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1689+1022A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051780 | ||||||
| chr8:100051780
|
T | C | 1 | a0002c0002t0001g0096 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1689+1022A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051780 | ||||||
| chr8:100051781
|
T | A | 9 | a0001c0009t0001g0100a0001c0009t0001g0101a0002c0002t0001g0086others(6): Show | 9 | HG01081.hp1 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1689+1021A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051781 | ||||||
| chr8:100051781
|
T | G | 1 | a0002c0002t0001g0096 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1689+1021A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051781 | ||||||
| chr8:100051782
|
T | A | 3 | a0002c0002t0001g0086a0002c0002t0001g0088a0005c0006t0001g0091 | 3 | NA18946.hp2 NA18965.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1689+1020A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051782 | ||||||
| chr8:100051784
|
T | A | 2 | a0001c0009t0001g0100a0001c0009t0001g0101 | 2 | HG02486.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1689+1018A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051784 | ||||||
| chr8:100051785
|
A | T | 1 | a0010c0015t0001g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1689+1017T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051785 | ||||||
| chr8:100051787
|
A | G | 2 | a0001c0009t0001g0100a0001c0009t0001g0101 | 2 | HG02486.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1689+1015T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051787 | ||||||
| chr8:100051787
|
A | T | 1 | a0003c0005t0001g0059 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1689+1015T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051787 | ||||||
| chr8:100051789
|
A | AATAT | 6 | a0002c0002t0001g0087a0002c0002t0001g0133a0002c0002t0001g0151others(3): Show | 6 | HG04184.hp2 NA18747.hp2 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.1689+1012_1689+101 others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051789 | ||||||
| chr8:100051789
|
A | T | 4 | a0001c0009t0001g0100a0001c0009t0001g0101a0005c0006t0001g0082others(1): Show | 4 | HG01081.hp1 HG02486.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1689+1013T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051789 | ||||||
| chr8:100051790
|
A | AATGTTT | 5 | a0001c0001t0001g0093a0001c0001t0001g0202a0001c0001t0001g0246others(2): Show | 5 | NA18968.hp1 NA18978.hp2 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.1689+1011_1689+101 others(10): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051790 | ||||||
| chr8:100051790
|
A | C | 14 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(11): Show | 14 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1689+1012T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051790 | ||||||
| chr8:100051790
|
A | T | 10 | a0001c0003t0001g0009a0001c0009t0001g0100a0001c0009t0001g0101others(7): Show | 10 | HG01081.hp1 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1689+1012T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051790 | ||||||
| chr8:100051790
|
AATATATA others(17): Show |
A | 32 | a0001c0001t0001g0008a0001c0001t0001g0037a0001c0001t0001g0066others(29): Show | 32 | HG00597.hp2 HG00733.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1689+988_1689+1011 others(27): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051790 | ||||||
| chr8:100051791
|
A | ATGTTTAT others(5): Show |
1 | a0001c0001t0001g0284 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1689+1010_1689+101 others(16): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051791 | ||||||
| chr8:100051791
|
A | ATGTTTAT others(223): Show |
1 | a0001c0001t0003g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1689+1010_1689+101 others(234): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051791 | ||||||
| chr8:100051791
|
A | G | 14 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(11): Show | 14 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1689+1011T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051791 | ||||||
| chr8:100051791
|
A | T | 3 | a0001c0003t0001g0009a0002c0002t0001g0086a0002c0002t0001g0088 | 3 | NA18946.hp2 NA18965.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1689+1011T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051791 | ||||||
| chr8:100051791
|
ATATATAT others(47): Show |
A | 74 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0036others(71): Show | 74 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.1689+957_1689+1010 others(57): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051791 | ||||||
| chr8:100051794
|
T | A | 1 | a0010c0015t0001g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1689+1008A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051794 | ||||||
| chr8:100051796
|
T | A | 7 | a0002c0002t0001g0087a0002c0002t0001g0133a0002c0002t0001g0151others(4): Show | 7 | HG02280.hp1 HG04184.hp2 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.1689+1006A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051796 | ||||||
| chr8:100051796
|
T | C | 1 | a0005c0006t0001g0091 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1689+1006A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051796 | ||||||
| chr8:100051797
|
A | G | 1 | a0010c0015t0001g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1689+1005T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051797 | ||||||
| chr8:100051798
|
T | C | 17 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(14): Show | 17 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.1689+1004A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051798 | ||||||
| chr8:100051799
|
T | A | 7 | a0002c0002t0001g0087a0002c0002t0001g0133a0002c0002t0001g0151others(4): Show | 7 | HG04184.hp2 NA18747.hp2 NA18991.hp1 others(4): Show |
intron_variant | MODIFIER | c.1689+1003A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051799 | ||||||
| chr8:100051799
|
T | G | 18 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(15): Show | 18 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1689+1003A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051799 | ||||||
| chr8:100051799
|
TTATATAT others(9): Show |
T | 3 | a0001c0001t0001g0198a0001c0001t0001g0215a0001c0001t0001g0294 | 3 | HG00099.hp2 HG02698.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1689+987_1689+1002 others(19): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051799 | ||||||
| chr8:100051800
|
T | A | 6 | a0002c0002t0001g0087a0002c0002t0001g0133a0002c0002t0001g0151others(3): Show | 6 | HG04184.hp2 NA18747.hp2 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.1689+1002A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051800 | ||||||
| chr8:100051801
|
A | T | 1 | a0003c0005t0001g0059 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1689+1001T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051801 | ||||||
| chr8:100051803
|
A | ATATACG | 14 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(11): Show | 14 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1689+998_1689+999i others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051803 | ||||||
| chr8:100051804
|
T | A | 1 | a0005c0006t0001g0091 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1689+998A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051804 | ||||||
| chr8:100051807
|
A | T | 1 | a0010c0015t0001g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1689+995T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051807 | ||||||
| chr8:100051808
|
A | T | 16 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(13): Show | 16 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.1689+994T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051808 | ||||||
| chr8:100051810
|
T | C | 14 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(11): Show | 14 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1689+992A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051810 | ||||||
| chr8:100051811
|
G | A | 11 | a0002c0002t0001g0087a0002c0002t0001g0096a0002c0002t0001g0133others(8): Show | 11 | HG01081.hp1 HG03540.hp1 HG04184.hp2 others(8): Show |
intron_variant | MODIFIER | c.1689+991C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051811 | ||||||
| chr8:100051812
|
T | TATAAATA others(65): Show |
6 | a0002c0002t0001g0087a0002c0002t0001g0133a0002c0002t0001g0151others(3): Show | 6 | HG04184.hp2 NA18747.hp2 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.1689+989_1689+990i others(74): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051812 | ||||||
| chr8:100051813
|
T | A | 18 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(15): Show | 18 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1689+989A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051813 | ||||||
| chr8:100051813
|
T | G | 6 | a0002c0002t0001g0087a0002c0002t0001g0133a0002c0002t0001g0151others(3): Show | 6 | HG04184.hp2 NA18747.hp2 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.1689+989A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051813 | ||||||
| chr8:100051813
|
TTA | T | 23 | a0001c0001t0001g0029a0001c0001t0001g0097a0001c0001t0001g0145others(20): Show | 23 | HG00597.hp1 HG00738.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.1689+987_1689+988d others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051813 | ||||||
| chr8:100051815
|
A | ATATATAT others(23): Show |
3 | a0001c0001t0001g0026a0001c0001t0001g0237a0001c0001t0001g0254 | 3 | NA18984.hp2 NA19076.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1689+957_1689+986d others(32): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051815 | ||||||
| chr8:100051815
|
A | ATATATT | 33 | a0000c0019t0001g0248a0001c0001t0001g0018a0001c0001t0001g0019others(30): Show | 33 | HG00099.hp1 HG00673.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.1689+986_1689+987i others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051815 | ||||||
| chr8:100051815
|
A | ATT | 3 | a0002c0002t0001g0096a0005c0006t0001g0082a0005c0006t0001g0092 | 3 | HG01081.hp1 NA18966.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1689+986_1689+987i others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051815 | ||||||
| chr8:100051815
|
A | T | 2 | a0003c0005t0001g0059a0010c0015t0001g0117 | 2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1689+987T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051815 | ||||||
| chr8:100051815
|
ATATATAT others(23): Show |
A | 2 | a0001c0001t0001g0296a0001c0001t0004g0142 | 2 | HG01993.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1689+957_1689+986d others(32): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051815 | ||||||
| chr8:100051817
|
ATATATTT others(135): Show |
A | 1 | a0001c0003t0001g0009 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1689+843_1689+984d others(2): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051817 | ||||||
| chr8:100051819
|
A | ACG | 14 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(11): Show | 14 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1689+982_1689+983i others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051819 | ||||||
| chr8:100051819
|
A | ATT | 4 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(1): Show | 4 | HG02735.hp1 HG03831.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1689+982_1689+983i others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051819 | ||||||
| chr8:100051822
|
T | C | 7 | a0002c0002t0001g0087a0002c0002t0001g0133a0002c0002t0001g0151others(4): Show | 7 | HG04184.hp2 NA18747.hp2 NA18991.hp1 others(4): Show |
intron_variant | MODIFIER | c.1689+980A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051822 | ||||||
| chr8:100051823
|
T | A | 18 | a0000c0021t0001g0150a0001c0001t0001g0070a0001c0001t0001g0072others(15): Show | 18 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.1689+979A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051823 | ||||||
| chr8:100051823
|
T | G | 7 | a0002c0002t0001g0087a0002c0002t0001g0133a0002c0002t0001g0151others(4): Show | 7 | HG04184.hp2 NA18747.hp2 NA18991.hp1 others(4): Show |
intron_variant | MODIFIER | c.1689+979A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051823 | ||||||
| chr8:100051825
|
A | T | 1 | a0002c0002t0001g0088 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1689+977T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051825 | ||||||
| chr8:100051827
|
A | ACG | 14 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(11): Show | 14 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1689+974_1689+975i others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051827 | ||||||
| chr8:100051829
|
ATAAATG | A | 23 | a0001c0001t0001g0029a0001c0001t0001g0097a0001c0001t0001g0145others(20): Show | 23 | HG00597.hp1 HG00738.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.1689+967_1689+972d others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051829 | ||||||
| chr8:100051832
|
A | T | 14 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(11): Show | 14 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1689+970T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051832 | ||||||
| chr8:100051833
|
ATGTT | A | 7 | a0002c0002t0001g0087a0002c0002t0001g0133a0002c0002t0001g0151others(4): Show | 7 | HG04184.hp2 NA18747.hp2 NA18991.hp1 others(4): Show |
intron_variant | MODIFIER | c.1689+965_1689+968d others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051833 | ||||||
| chr8:100051833
|
ATGTTTAT others(5): Show |
A | 2 | a0001c0001t0001g0022a0001c0001t0001g0211 | 2 | HG00621.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.1689+957_1689+968d others(14): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051833 | ||||||
| chr8:100051835
|
G | A | 16 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(13): Show | 16 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.1689+967C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051835 | ||||||
| chr8:100051835
|
G | GTTTATAT others(1): Show |
4 | a0001c0001t0001g0193a0001c0001t0001g0215a0001c0001t0001g0294others(1): Show | 4 | HG00735.hp1 HG02698.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1689+959_1689+966d others(10): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051835 | ||||||
| chr8:100051836
|
T | A | 14 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(11): Show | 14 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1689+966A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051836 | ||||||
| chr8:100051837
|
T | A | 14 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(11): Show | 14 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1689+965A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051837 | ||||||
| chr8:100051843
|
ATT | A | 23 | a0001c0001t0001g0029a0001c0001t0001g0097a0001c0001t0001g0145others(20): Show | 23 | HG00597.hp1 HG00738.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.1689+957_1689+958d others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051843 | ||||||
| chr8:100051843
|
ATTTATAT others(15): Show |
A | 1 | a0001c0001t0001g0198 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1689+937_1689+958d others(24): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051843 | ||||||
| chr8:100051845
|
T | A | 5 | a0002c0002t0001g0086a0002c0002t0001g0088a0002c0002t0001g0096others(2): Show | 5 | HG01081.hp1 NA18946.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1689+957A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051845 | ||||||
| chr8:100051847
|
A | T | 3 | a0002c0002t0001g0096a0005c0006t0001g0082a0005c0006t0001g0092 | 3 | HG01081.hp1 NA18966.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1689+955T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051847 | ||||||
| chr8:100051848
|
T | A | 23 | a0001c0001t0001g0029a0001c0001t0001g0097a0001c0001t0001g0145others(20): Show | 23 | HG00597.hp1 HG00738.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.1689+954A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051848 | ||||||
| chr8:100051851
|
A | G | 23 | a0001c0001t0001g0029a0001c0001t0001g0097a0001c0001t0001g0145others(20): Show | 23 | HG00597.hp1 HG00738.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.1689+951T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051851 | ||||||
| chr8:100051853
|
T | A | 3 | a0002c0002t0001g0096a0005c0006t0001g0082a0005c0006t0001g0092 | 3 | HG01081.hp1 NA18966.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1689+949A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051853 | ||||||
| chr8:100051856
|
T | A | 3 | a0002c0002t0001g0096a0005c0006t0001g0082a0005c0006t0001g0092 | 3 | HG01081.hp1 NA18966.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1689+946A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051856 | ||||||
| chr8:100051859
|
ATAAATG | A | 24 | a0001c0001t0001g0029a0001c0001t0001g0097a0001c0001t0001g0138others(21): Show | 24 | HG00597.hp1 HG00738.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.1689+937_1689+942d others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051859 | ||||||
| chr8:100051862
|
A | T | 3 | a0002c0002t0001g0096a0005c0006t0001g0082a0005c0006t0001g0092 | 3 | HG01081.hp1 NA18966.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1689+940T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051862 | ||||||
| chr8:100051865
|
G | T | 3 | a0002c0002t0001g0096a0005c0006t0001g0082a0005c0006t0001g0092 | 3 | HG01081.hp1 NA18966.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1689+937C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051865 | ||||||
| chr8:100051867
|
T | A | 3 | a0002c0002t0001g0096a0005c0006t0001g0082a0005c0006t0001g0092 | 3 | HG01081.hp1 NA18966.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1689+935A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051867 | ||||||
| chr8:100051867
|
T | TTA | 3 | a0001c0001t0003g0003a0003c0005t0001g0059a0010c0015t0001g0117 | 3 | HG01243.hp2 HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1689+933_1689+934d others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051867 | ||||||
| chr8:100051873
|
ATT | A | 4 | a0001c0001t0001g0138a0001c0001t0001g0193a0001c0001t0001g0215others(1): Show | 4 | HG00735.hp1 HG01109.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1689+927_1689+928d others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051873 | ||||||
| chr8:100051873
|
ATTTATAT others(15): Show |
A | 2 | a0001c0012t0001g0131a0002c0002t0001g0289 | 2 | HG02976.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1689+907_1689+928d others(24): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051873 | ||||||
| chr8:100051874
|
T | A | 3 | a0002c0002t0001g0096a0005c0006t0001g0082a0005c0006t0001g0092 | 3 | HG01081.hp1 NA18966.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1689+928A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051874 | ||||||
| chr8:100051875
|
T | A | 24 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(21): Show | 24 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.1689+927A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051875 | ||||||
| chr8:100051877
|
A | T | 21 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(18): Show | 21 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.1689+925T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051877 | ||||||
| chr8:100051878
|
T | A | 1 | a0001c0001t0001g0138 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1689+924A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051878 | ||||||
| chr8:100051881
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1689+921T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051881 | ||||||
| chr8:100051883
|
T | A | 21 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(18): Show | 21 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.1689+919A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051883 | ||||||
| chr8:100051886
|
T | A | 21 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(18): Show | 21 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.1689+916A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051886 | ||||||
| chr8:100051889
|
ATAAATG | A | 4 | a0001c0001t0001g0200a0004c0008t0001g0173a0004c0008t0001g0189others(1): Show | 4 | NA18970.hp1 NA19058.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.1689+907_1689+912d others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051889 | ||||||
| chr8:100051892
|
A | T | 22 | a0000c0021t0001g0150a0001c0001t0001g0138a0002c0002t0001g0033others(19): Show | 22 | HG00558.hp2 HG00673.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1689+910T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051892 | ||||||
| chr8:100051894
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1689+908A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051894 | ||||||
| chr8:100051895
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1689+907C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051895 | ||||||
| chr8:100051895
|
G | GTTTATAT others(1): Show |
10 | a0000c0019t0001g0248a0001c0001t0001g0022a0001c0001t0001g0047others(7): Show | 10 | HG00673.hp1 HG02027.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1689+899_1689+906d others(10): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051895 | ||||||
| chr8:100051895
|
G | T | 21 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(18): Show | 21 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.1689+907C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051895 | ||||||
| chr8:100051897
|
T | A | 21 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(18): Show | 21 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.1689+905A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051897 | ||||||
| chr8:100051897
|
T | TTA | 7 | a0001c0001t0001g0098a0001c0001t0001g0193a0001c0001t0001g0215others(4): Show | 7 | HG00735.hp1 HG01099.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.1689+903_1689+904d others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051897 | ||||||
| chr8:100051897
|
T | TTATATAT others(25): Show |
3 | a0001c0001t0001g0093a0001c0001t0001g0246a0001c0001t0001g0249 | 3 | NA18968.hp1 NA19000.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1689+873_1689+904d others(34): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051897 | ||||||
| chr8:100051897
|
T | TTATATAT others(119): Show |
1 | a0001c0003t0001g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1689+904_1689+905i others(128): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051897 | ||||||
| chr8:100051897
|
T | TTATATAT others(183): Show |
1 | a0001c0001t0001g0067 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1689+904_1689+905i others(192): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051897 | ||||||
| chr8:100051903
|
A | ATATTTAT others(19): Show |
1 | a0003c0005t0001g0060 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1689+898_1689+899i others(28): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051903 | ||||||
| chr8:100051903
|
ATT | A | 28 | a0001c0001t0001g0029a0001c0001t0001g0097a0001c0001t0001g0145others(25): Show | 28 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1689+897_1689+898d others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051903 | ||||||
| chr8:100051903
|
ATTTATAT others(47): Show |
A | 1 | a0001c0001t0001g0252 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1689+845_1689+898d others(56): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051903 | ||||||
| chr8:100051904
|
T | A | 21 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(18): Show | 21 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.1689+898A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051904 | ||||||
| chr8:100051905
|
T | A | 22 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(19): Show | 22 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.1689+897A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051905 | ||||||
| chr8:100051905
|
TTATATAT others(17): Show |
T | 1 | a0001c0001t0001g0194 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1689+873_1689+896d others(26): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051905 | ||||||
| chr8:100051905
|
TTATATAT others(105): Show |
T | 1 | a0001c0001t0001g0099 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1689+785_1689+896d others(2): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051905 | ||||||
| chr8:100051908
|
T | A | 4 | a0001c0001t0001g0200a0004c0008t0001g0173a0004c0008t0001g0189others(1): Show | 4 | NA18970.hp1 NA19058.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.1689+894A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051908 | ||||||
| chr8:100051911
|
A | G | 4 | a0001c0001t0001g0200a0004c0008t0001g0173a0004c0008t0001g0189others(1): Show | 4 | NA18970.hp1 NA19058.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.1689+891T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051911 | ||||||
| chr8:100051913
|
TTATATAT others(41): Show |
T | 10 | a0001c0001t0001g0004a0001c0001t0001g0048a0001c0001t0001g0049others(7): Show | 10 | HG01884.hp2 HG02630.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1689+841_1689+888d others(50): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051913 | ||||||
| chr8:100051919
|
ATAAATG | A | 68 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0135others(65): Show | 68 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.1689+877_1689+882d others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051919 | ||||||
| chr8:100051919
|
ATAAATGT others(1): Show |
A | 4 | a0001c0001t0001g0200a0004c0008t0001g0173a0004c0008t0001g0189others(1): Show | 4 | NA18970.hp1 NA19058.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.1689+875_1689+882d others(10): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051919 | ||||||
| chr8:100051927
|
TTA | T | 45 | a0000c0021t0001g0150a0001c0001t0001g0037a0001c0001t0001g0041others(42): Show | 45 | HG00099.hp1 HG00558.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.1689+873_1689+874d others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051927 | ||||||
| chr8:100051929
|
A | ATATATT | 4 | a0001c0001t0001g0282a0002c0002t0001g0096a0005c0006t0001g0082others(1): Show | 4 | HG01081.hp1 HG02027.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.1689+872_1689+873i others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051929 | ||||||
| chr8:100051929
|
A | T | 4 | a0001c0001t0001g0200a0004c0008t0001g0173a0004c0008t0001g0189others(1): Show | 4 | NA18970.hp1 NA19058.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.1689+873T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051929 | ||||||
| chr8:100051931
|
ATATATTT others(21): Show |
A | 20 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0019others(17): Show | 20 | HG01071.hp2 HG01074.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.1689+843_1689+870d others(30): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051931 | ||||||
| chr8:100051933
|
ATATT | A | 71 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0034others(68): Show | 71 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.1689+865_1689+868d others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051933 | ||||||
| chr8:100051937
|
TTATATAT others(17): Show |
T | 26 | a0001c0001t0001g0029a0001c0001t0001g0097a0001c0001t0001g0145others(23): Show | 26 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.1689+841_1689+864d others(26): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051937 | ||||||
| chr8:100051940
|
T | A | 68 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0135others(65): Show | 68 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.1689+862A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051940 | ||||||
| chr8:100051943
|
A | G | 68 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0135others(65): Show | 68 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.1689+859T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051943 | ||||||
| chr8:100051945
|
T | A | 2 | a0001c0001t0001g0215a0001c0001t0001g0294 | 2 | HG02698.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1689+857A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051945 | ||||||
| chr8:100051945
|
TTATATAT others(9): Show |
T | 23 | a0001c0001t0001g0037a0001c0001t0001g0118a0001c0001t0001g0128others(20): Show | 23 | HG00597.hp2 HG00733.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.1689+841_1689+856d others(18): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051945 | ||||||
| chr8:100051946
|
T | A | 2 | a0001c0001t0001g0215a0001c0001t0001g0294 | 2 | HG02698.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1689+856A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051946 | ||||||
| chr8:100051949
|
A | G | 2 | a0001c0001t0001g0215a0001c0001t0001g0294 | 2 | HG02698.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1689+853T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051949 | ||||||
| chr8:100051949
|
ATATAAAT others(3): Show |
A | 63 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0135others(60): Show | 63 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.1689+843_1689+852d others(12): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051949 | ||||||
| chr8:100051951
|
A | T | 2 | a0001c0001t0001g0215a0001c0001t0001g0294 | 2 | HG02698.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1689+851T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051951 | ||||||
| chr8:100051953
|
AAATGTT | A | 4 | a0001c0004t0002g0121a0001c0004t0002g0122a0002c0002t0001g0086others(1): Show | 4 | HG02615.hp1 HG03195.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1689+843_1689+848d others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051953 | ||||||
| chr8:100051954
|
A | T | 2 | a0001c0001t0001g0215a0001c0001t0001g0294 | 2 | HG02698.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1689+848T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051954 | ||||||
| chr8:100051954
|
AATGTTTA others(3): Show |
A | 1 | a0001c0001t0001g0211 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1689+838_1689+847d others(12): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051954 | ||||||
| chr8:100051957
|
G | A | 2 | a0001c0001t0001g0215a0001c0001t0001g0294 | 2 | HG02698.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1689+845C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051957 | ||||||
| chr8:100051959
|
T | A | 3 | a0001c0001t0001g0215a0001c0001t0001g0252a0001c0001t0001g0294 | 3 | HG02027.hp1 HG02698.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1689+843A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051959 | ||||||
| chr8:100051959
|
T | TTATA | 5 | a0001c0001t0001g0041a0001c0001t0001g0200a0004c0008t0001g0173others(2): Show | 5 | HG00099.hp1 NA18970.hp1 NA19058.hp2 others(2): Show |
intron_variant | MODIFIER | c.1689+839_1689+842d others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051959 | ||||||
| chr8:100051961
|
A | ATATATAT others(1): Show |
31 | a0000c0019t0001g0248a0001c0001t0001g0022a0001c0001t0001g0047others(28): Show | 32 | HG00673.hp1 HG00735.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.1689+833_1689+840d others(10): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051961 | ||||||
| chr8:100051961
|
A | ATATATAT others(25): Show |
1 | a0001c0001t0001g0166 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1689+809_1689+840d others(34): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051961 | ||||||
| chr8:100051961
|
A | ATATATAT others(49): Show |
1 | a0001c0001t0001g0298 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1689+840_1689+841i others(58): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051961 | ||||||
| chr8:100051961
|
A | ATATATAT others(57): Show |
6 | a0003c0005t0001g0057a0003c0005t0001g0068a0003c0005t0001g0094others(3): Show | 6 | HG02451.hp2 HG02559.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1689+777_1689+840d others(66): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051961 | ||||||
| chr8:100051961
|
A | ATATATAT others(189): Show |
1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1689+840_1689+841i others(198): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051961 | ||||||
| chr8:100051961
|
A | ATATATTT others(7): Show |
21 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(18): Show | 21 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.1689+840_1689+841i others(16): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051961 | ||||||
| chr8:100051961
|
A | T | 7 | a0001c0001t0001g0215a0001c0001t0001g0252a0001c0001t0001g0294others(4): Show | 7 | HG02027.hp1 HG02615.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.1689+841T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051961 | ||||||
| chr8:100051961
|
ATATATAT others(25): Show |
A | 1 | a0001c0001t0001g0230 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1689+809_1689+840d others(34): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051961 | ||||||
| chr8:100051989
|
A | ATTTATAT others(53): Show |
1 | a0001c0001t0001g0224 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1689+812_1689+813i others(62): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051989 | ||||||
| chr8:100051991
|
A | T | 1 | a0001c0001t0001g0224 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1689+811T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051991 | ||||||
| chr8:100051993
|
T | A | 1 | a0001c0001t0001g0224 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1689+809A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100051993 | ||||||
| chr8:100052045
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1689+757C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052045 | ||||||
| chr8:100052047
|
T | A | 1 | a0001c0001t0001g0193 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1689+755A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052047 | ||||||
| chr8:100052050
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1689+752A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052050 | ||||||
| chr8:100052065
|
T | A | 1 | a0001c0001t0001g0193 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1689+737A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052065 | ||||||
| chr8:100052066
|
T | A | 1 | a0001c0001t0001g0193 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1689+736A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052066 | ||||||
| chr8:100052076
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1689+726A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052076 | ||||||
| chr8:100052077
|
G | A | 10 | a0001c0001t0001g0022a0001c0001t0001g0145a0001c0001t0001g0158others(7): Show | 10 | HG00735.hp1 HG00738.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1689+725C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052077 | ||||||
| chr8:100052079
|
T | A | 10 | a0001c0001t0001g0022a0001c0001t0001g0145a0001c0001t0001g0158others(7): Show | 10 | HG00735.hp1 HG00738.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1689+723A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052079 | ||||||
| chr8:100052080
|
T | TAA | 9 | a0001c0001t0001g0022a0001c0001t0001g0145a0001c0001t0001g0158others(6): Show | 9 | HG00738.hp1 HG01175.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.1689+721_1689+722i others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052080 | ||||||
| chr8:100052082
|
T | C | 9 | a0001c0001t0001g0022a0001c0001t0001g0145a0001c0001t0001g0158others(6): Show | 9 | HG00738.hp1 HG01175.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.1689+720A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052082 | ||||||
| chr8:100052083
|
A | T | 1 | a0001c0001t0001g0193 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1689+719T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052083 | ||||||
| chr8:100052084
|
T | A | 1 | a0001c0001t0001g0193 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1689+718A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052084 | ||||||
| chr8:100052089
|
T | A | 1 | a0001c0001t0001g0193 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1689+713A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052089 | ||||||
| chr8:100052089
|
T | TAA | 9 | a0001c0001t0001g0022a0001c0001t0001g0145a0001c0001t0001g0158others(6): Show | 9 | HG00738.hp1 HG01175.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.1689+712_1689+713i others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052089 | ||||||
| chr8:100052089
|
T | TTATATAT others(17): Show |
2 | a0001c0001t0001g0111a0001c0001t0001g0298 | 2 | HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1689+689_1689+712d others(26): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052089 | ||||||
| chr8:100052089
|
TTATATAT others(17): Show |
T | 24 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0018others(21): Show | 24 | HG01071.hp2 HG01074.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1689+689_1689+712d others(26): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052089 | ||||||
| chr8:100052094
|
T | A | 1 | a0001c0001t0001g0193 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1689+708A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052094 | ||||||
| chr8:100052097
|
T | A | 10 | a0001c0001t0001g0022a0001c0001t0001g0145a0001c0001t0001g0158others(7): Show | 10 | HG00735.hp1 HG00738.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1689+705A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052097 | ||||||
| chr8:100052098
|
T | A | 9 | a0001c0001t0001g0022a0001c0001t0001g0145a0001c0001t0001g0158others(6): Show | 9 | HG00738.hp1 HG01175.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.1689+704A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052098 | ||||||
| chr8:100052102
|
T | A | 1 | a0001c0001t0001g0193 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1689+700A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052102 | ||||||
| chr8:100052104
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1689+698A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052104 | ||||||
| chr8:100052106
|
A | AACAT | 9 | a0001c0001t0001g0022a0001c0001t0001g0145a0001c0001t0001g0158others(6): Show | 9 | HG00738.hp1 HG01175.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.1689+695_1689+696i others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052106 | ||||||
| chr8:100052106
|
A | T | 1 | a0001c0001t0001g0193 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1689+696T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052106 | ||||||
| chr8:100052109
|
G | A | 49 | a0000c0019t0001g0248a0001c0001t0001g0021a0001c0001t0001g0022others(46): Show | 49 | HG00099.hp1 HG00621.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1689+693C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052109 | ||||||
| chr8:100052111
|
T | A | 49 | a0000c0019t0001g0248a0001c0001t0001g0021a0001c0001t0001g0022others(46): Show | 49 | HG00099.hp1 HG00621.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1689+691A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052111 | ||||||
| chr8:100052112
|
T | A | 10 | a0001c0001t0001g0022a0001c0001t0001g0145a0001c0001t0001g0158others(7): Show | 10 | HG00735.hp1 HG00738.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1689+690A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052112 | ||||||
| chr8:100052112
|
T | TAA | 38 | a0000c0019t0001g0248a0001c0001t0001g0021a0001c0001t0001g0029others(35): Show | 38 | HG00099.hp1 HG00621.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.1689+689_1689+690i others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052112 | ||||||
| chr8:100052113
|
A | ATATATAT others(1): Show |
126 | a0000c0021t0001g0150a0001c0001t0001g0019a0001c0001t0001g0020others(123): Show | 126 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1689+681_1689+688d others(10): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052113 | ||||||
| chr8:100052114
|
T | C | 38 | a0000c0019t0001g0248a0001c0001t0001g0021a0001c0001t0001g0029others(35): Show | 38 | HG00099.hp1 HG00621.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.1689+688A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052114 | ||||||
| chr8:100052118
|
T | A | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1689+684A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052118 | ||||||
| chr8:100052121
|
T | A | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1689+681A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052121 | ||||||
| chr8:100052121
|
T | TAA | 38 | a0000c0019t0001g0248a0001c0001t0001g0021a0001c0001t0001g0029others(35): Show | 38 | HG00099.hp1 HG00621.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.1689+680_1689+681i others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052121 | ||||||
| chr8:100052129
|
A | T | 4 | a0001c0001t0001g0224a0001c0001t0001g0284a0001c0009t0001g0100others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1689+673T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052129 | ||||||
| chr8:100052130
|
A | T | 4 | a0001c0001t0001g0224a0001c0001t0001g0284a0001c0009t0001g0100others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1689+672T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052130 | ||||||
| chr8:100052147
|
T | A | 47 | a0000c0019t0001g0248a0001c0001t0001g0021a0001c0001t0001g0022others(44): Show | 47 | HG00099.hp1 HG00621.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.1689+655A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052147 | ||||||
| chr8:100052150
|
T | A | 1 | a0001c0001t0001g0278 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1689+652A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052150 | ||||||
| chr8:100052150
|
T | TATATATA others(13): Show |
1 | a0010c0015t0001g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1689+632_1689+651d others(22): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052150 | ||||||
| chr8:100052152
|
T | TATATAAA others(9): Show |
149 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0008others(146): Show | 149 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.1689+649_1689+650i others(18): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052152 | ||||||
| chr8:100052152
|
T | TATATATA others(11): Show |
10 | a0001c0001t0001g0134a0003c0005t0001g0002a0003c0005t0001g0059others(7): Show | 11 | HG01109.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1689+632_1689+649d others(20): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052152 | ||||||
| chr8:100052152
|
T | TATATATA others(29): Show |
1 | a0001c0001t0001g0284 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1689+614_1689+649d others(38): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052152 | ||||||
| chr8:100052152
|
T | TATATATA others(47): Show |
2 | a0001c0009t0001g0100a0001c0009t0001g0101 | 2 | HG02486.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1689+596_1689+649d others(56): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052152 | ||||||
| chr8:100052157
|
A | T | 46 | a0000c0019t0001g0248a0001c0001t0001g0021a0001c0001t0001g0022others(43): Show | 46 | HG00099.hp1 HG00673.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1689+645T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052157 | ||||||
| chr8:100052158
|
TAAATATA others(5): Show |
T | 46 | a0000c0019t0001g0248a0001c0001t0001g0021a0001c0001t0001g0022others(43): Show | 46 | HG00099.hp1 HG00673.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1689+632_1689+643d others(14): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052158 | ||||||
| chr8:100052168
|
A | T | 150 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0008others(147): Show | 150 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.1689+634T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052168 | ||||||
| chr8:100052169
|
A | T | 150 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0008others(147): Show | 150 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.1689+633T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052169 | ||||||
| chr8:100052170
|
C | CATATATA others(11): Show |
2 | a0001c0001t0001g0211a0001c0001t0001g0278 | 2 | HG00621.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1689+631_1689+632i others(20): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052170 | ||||||
| chr8:100052170
|
C | T | 150 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0008others(147): Show | 150 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.1689+632G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052170 | ||||||
| chr8:100052210
|
T | TAAATATA others(5): Show |
1 | a0001c0001t0003g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1689+591_1689+592i others(14): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052210 | ||||||
| chr8:100052214
|
A | AAT | 7 | a0003c0005t0001g0057a0003c0005t0001g0060a0003c0005t0001g0068others(4): Show | 7 | HG02451.hp2 HG02559.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1689+586_1689+587d others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052214 | ||||||
| chr8:100052214
|
A | AATATATA others(7): Show |
2 | a0001c0001t0001g0067a0001c0003t0001g0005 | 2 | HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1689+587_1689+588i others(16): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052214 | ||||||
| chr8:100052214
|
A | T | 1 | a0001c0001t0003g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1689+588T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052214 | ||||||
| chr8:100052220
|
C | A | 7 | a0003c0005t0001g0057a0003c0005t0001g0060a0003c0005t0001g0068others(4): Show | 7 | HG02451.hp2 HG02559.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1689+582G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052220 | ||||||
| chr8:100052225
|
ATATATG | A | 9 | a0003c0005t0001g0002a0003c0005t0001g0059a0003c0005t0001g0061others(6): Show | 10 | HG02280.hp1 HG02486.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1689+571_1689+576d others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052225 | ||||||
| chr8:100052228
|
T | TAAATATA others(3): Show |
7 | a0003c0005t0001g0057a0003c0005t0001g0060a0003c0005t0001g0068others(4): Show | 7 | HG02451.hp2 HG02559.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1689+573_1689+574i others(12): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052228 | ||||||
| chr8:100052231
|
G | A | 7 | a0003c0005t0001g0057a0003c0005t0001g0060a0003c0005t0001g0068others(4): Show | 7 | HG02451.hp2 HG02559.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1689+571C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052231 | ||||||
| chr8:100052289
|
A | T | 1 | a0001c0001t0001g0284 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1689+513T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052289 | ||||||
| chr8:100052291
|
T | A | 1 | a0001c0001t0001g0284 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1689+511A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052291 | ||||||
| chr8:100052341
|
C | G | 16 | a0003c0005t0001g0002a0003c0005t0001g0057a0003c0005t0001g0059others(13): Show | 17 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.1689+461G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052341 | ||||||
| chr8:100052395
|
G | A | 3 | a0001c0001t0001g0284a0001c0009t0001g0100a0001c0009t0001g0101 | 3 | HG02486.hp2 HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1689+407C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052395 | ||||||
| chr8:100052416
|
C | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0099 | 2 | HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1689+386G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052416 | ||||||
| chr8:100052427
|
G | A | 1 | a0001c0001t0001g0250 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1689+375C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052427 | ||||||
| chr8:100052442
|
C | T | 1 | a0001c0001t0001g0161 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1689+360G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052442 | ||||||
| chr8:100052447
|
G | A | 1 | a0001c0001t0003g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1689+355C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052447 | ||||||
| chr8:100052469
|
T | A | 1 | a0001c0001t0001g0138 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1689+333A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052469 | ||||||
| chr8:100052550
|
C | A | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1689+252G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052550 | ||||||
| chr8:100052595
|
C | T | 36 | a0000c0019t0001g0248a0001c0001t0001g0037a0001c0001t0001g0047others(33): Show | 36 | HG00597.hp2 HG00673.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.1689+207G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052595 | ||||||
| chr8:100052647
|
A | T | 12 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0039others(9): Show | 12 | HG01071.hp2 HG01074.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.1689+155T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052647 | ||||||
| chr8:100052751
|
C | T | 2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1689+51G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052751 | ||||||
| chr8:100052794
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG03041.hp1 | splice_region_variant&intron_variant | LOW | c.1689+8G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 10/27 | chr8 | 100052794 | ||||||
| chr8:100053083
|
T | C | 7 | a0001c0001t0001g0232a0001c0001t0001g0234a0001c0001t0001g0235others(4): Show | 7 | HG00408.hp2 NA18960.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.1515-107A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100053083 | ||||||
| chr8:100053152
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1515-176A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100053152 | ||||||
| chr8:100053196
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1515-220A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100053196 | ||||||
| chr8:100053290
|
T | C | 199 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.1515-314A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100053290 | ||||||
| chr8:100053294
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1515-318G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100053294 | ||||||
| chr8:100053336
|
T | C | 208 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(205): Show | 209 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.1515-360A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100053336 | ||||||
| chr8:100053424
|
A | G | 2 | a0001c0001t0001g0233a0001c0001t0001g0247 | 2 | HG01255.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1515-448T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100053424 | ||||||
| chr8:100053446
|
A | AAGGGAGG others(1): Show |
204 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(201): Show | 205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.1515-478_1515-471d others(10): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100053446 | ||||||
| chr8:100053460
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1515-484C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100053460 | ||||||
| chr8:100053464
|
G | A | 14 | a0001c0001t0001g0047a0001c0001t0001g0280a0001c0003t0001g0074others(11): Show | 14 | HG00597.hp2 HG02145.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1515-488C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100053464 | ||||||
| chr8:100053486
|
GA | G | 5 | a0001c0001t0001g0204a0001c0001t0001g0218a0001c0001t0001g0223others(2): Show | 5 | HG01074.hp1 HG01099.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.1515-511delT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100053486 | ||||||
| chr8:100053540
|
T | C | 1 | a0001c0001t0001g0297 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1515-564A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100053540 | ||||||
| chr8:100053836
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1515-860T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100053836 | ||||||
| chr8:100053843
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1515-867G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100053843 | ||||||
| chr8:100054054
|
G | C | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1515-1078C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100054054 | ||||||
| chr8:100054071
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1515-1095C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100054071 | ||||||
| chr8:100054913
|
C | T | 2 | a0010c0015t0001g0117a0011c0016t0001g0132 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1515-1937G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100054913 | ||||||
| chr8:100055025
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1515-2049G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100055025 | ||||||
| chr8:100055418
|
C | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0103others(4): Show | 7 | HG01884.hp2 HG02630.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1515-2442G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100055418 | ||||||
| chr8:100055423
|
T | G | 2 | a0010c0015t0001g0117a0011c0016t0001g0132 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1515-2447A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100055423 | ||||||
| chr8:100055687
|
A | T | 139 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0022others(136): Show | 139 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.1515-2711T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100055687 | ||||||
| chr8:100055692
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1515-2716T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100055692 | ||||||
| chr8:100055821
|
C | A | 2 | a0010c0015t0001g0117a0011c0016t0001g0132 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1515-2845G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100055821 | ||||||
| chr8:100056335
|
G | T | 1 | a0001c0001t0001g0184 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1515-3359C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100056335 | ||||||
| chr8:100056452
|
C | A | 1 | a0001c0001t0001g0251 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1515-3476G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100056452 | ||||||
| chr8:100056458
|
C | A | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1515-3482G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100056458 | ||||||
| chr8:100056932
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1515-3956G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100056932 | ||||||
| chr8:100056959
|
C | T | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1515-3983G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100056959 | ||||||
| chr8:100057073
|
C | A | 2 | a0001c0004t0002g0121a0001c0004t0002g0122 | 2 | HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1515-4097G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100057073 | ||||||
| chr8:100057392
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1515-4416A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100057392 | ||||||
| chr8:100057531
|
C | T | 2 | a0010c0015t0001g0117a0011c0016t0001g0132 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1515-4555G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100057531 | ||||||
| chr8:100057791
|
CTTCAATG others(15): Show |
C | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+4778_1514+479 others(26): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100057791 | ||||||
| chr8:100057793
|
T | C | 1 | a0001c0001t0001g0298 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1514+4798A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100057793 | ||||||
| chr8:100057886
|
A | G | 2 | a0010c0015t0001g0117a0011c0016t0001g0132 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1514+4705T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100057886 | ||||||
| chr8:100058091
|
A | T | 2 | a0001c0012t0001g0112a0001c0012t0001g0131 | 2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1514+4500T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100058091 | ||||||
| chr8:100058125
|
A | C | 2 | a0001c0001t0001g0166a0001c0001t0001g0245 | 2 | HG01123.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1514+4466T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100058125 | ||||||
| chr8:100058171
|
C | CA | 6 | a0001c0001t0001g0134a0001c0001t0001g0298a0001c0001t0004g0142others(3): Show | 6 | HG01109.hp1 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1514+4419dupT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100058171 | ||||||
| chr8:100058171
|
CA | C | 8 | a0001c0001t0001g0102a0001c0001t0001g0275a0001c0003t0001g0001others(5): Show | 9 | HG01256.hp1 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1514+4419delT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100058171 | ||||||
| chr8:100058178
|
A | AC | 3 | a0001c0001t0001g0159a0001c0001t0001g0227a0001c0001t0001g0228 | 3 | HG02056.hp1 HG02683.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1514+4412_1514+441 others(5): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100058178 | ||||||
| chr8:100058181
|
A | AC | 160 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0008others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1514+4409_1514+441 others(5): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100058181 | ||||||
| chr8:100058181
|
A | C | 3 | a0001c0001t0001g0159a0001c0001t0001g0227a0001c0001t0001g0228 | 3 | HG02056.hp1 HG02683.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1514+4410T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100058181 | ||||||
| chr8:100058183
|
A | C | 5 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0024others(2): Show | 5 | NA18952.hp1 NA19063.hp2 NA19068.hp2 others(2): Show |
intron_variant | MODIFIER | c.1514+4408T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100058183 | ||||||
| chr8:100058184
|
A | C | 165 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0008others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.1514+4407T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100058184 | ||||||
| chr8:100058531
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1514+4060C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100058531 | ||||||
| chr8:100058602
|
C | T | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG02683.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1514+3989G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100058602 | ||||||
| chr8:100058969
|
G | A | 7 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0160others(4): Show | 7 | HG00558.hp1 HG02083.hp1 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.1514+3622C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100058969 | ||||||
| chr8:100059150
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1514+3441G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100059150 | ||||||
| chr8:100059414
|
T | TACAAACT others(41): Show |
1 | a0001c0001t0001g0097 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1514+3129_1514+317 others(52): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100059414 | ||||||
| chr8:100059690
|
G | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | NA18970.hp2 NA18973.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.1514+2901C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100059690 | ||||||
| chr8:100059955
|
G | A | 3 | a0003c0005t0001g0069a0003c0005t0001g0107a0003c0005t0001g0108 | 3 | HG02717.hp1 HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1514+2636C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100059955 | ||||||
| chr8:100060141
|
A | G | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | NA18955.hp2 NA19005.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1514+2450T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060141 | ||||||
| chr8:100060155
|
T | C | 3 | a0001c0001t0001g0067a0001c0001t0003g0003a0001c0003t0001g0005 | 3 | HG01243.hp2 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1514+2436A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060155 | ||||||
| chr8:100060292
|
G | C | 206 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.1514+2299C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060292 | ||||||
| chr8:100060402
|
G | GTA | 10 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0044others(7): Show | 10 | HG00621.hp2 HG00735.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.1514+2187_1514+218 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060402 | ||||||
| chr8:100060402
|
G | GTATATAT others(11): Show |
2 | a0001c0001t0001g0139a0001c0001t0001g0267 | 2 | HG00438.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.1514+2171_1514+218 others(22): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060402 | ||||||
| chr8:100060402
|
G | GTATATAT others(13): Show |
7 | a0001c0001t0001g0035a0001c0001t0001g0039a0001c0001t0001g0050others(4): Show | 7 | HG01071.hp2 HG01074.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.1514+2169_1514+218 others(24): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060402 | ||||||
| chr8:100060402
|
G | GTATATAT others(15): Show |
11 | a0001c0001t0001g0042a0001c0001t0001g0145a0001c0001t0001g0157others(8): Show | 11 | HG00558.hp1 HG00597.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.1514+2188_1514+218 others(26): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060402 | ||||||
| chr8:100060402
|
G | GTATATAT others(17): Show |
11 | a0001c0001t0001g0038a0001c0001t0001g0137a0001c0001t0001g0175others(8): Show | 11 | HG00609.hp1 HG01934.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.1514+2188_1514+218 others(28): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060402 | ||||||
| chr8:100060402
|
G | GTATATAT others(19): Show |
3 | a0001c0001t0001g0163a0001c0001t0001g0180a0001c0001t0001g0196 | 3 | HG01993.hp2 NA18952.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1514+2188_1514+218 others(30): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060402 | ||||||
| chr8:100060402
|
G | GTATATAT others(21): Show |
11 | a0001c0001t0001g0070a0001c0001t0001g0159a0001c0001t0001g0178others(8): Show | 11 | HG00621.hp1 HG01123.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1514+2188_1514+218 others(32): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060402 | ||||||
| chr8:100060402
|
G | GTATATAT others(23): Show |
20 | a0001c0001t0001g0022a0001c0001t0001g0072a0001c0001t0001g0073others(17): Show | 20 | HG00738.hp1 HG01074.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.1514+2188_1514+218 others(34): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060402 | ||||||
| chr8:100060402
|
G | GTATATAT others(25): Show |
7 | a0001c0001t0001g0040a0001c0001t0001g0144a0001c0001t0001g0164others(4): Show | 7 | HG01358.hp1 HG03669.hp2 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.1514+2188_1514+218 others(36): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060402 | ||||||
| chr8:100060402
|
G | GTATATAT others(27): Show |
4 | a0001c0001t0001g0300a0001c0001t0001g0302a0001c0001t0001g0303others(1): Show | 4 | NA18970.hp1 NA18977.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.1514+2188_1514+218 others(38): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060402 | ||||||
| chr8:100060402
|
G | GTATATAT others(29): Show |
7 | a0001c0001t0001g0034a0001c0001t0001g0174a0001c0001t0001g0217others(4): Show | 7 | HG00544.hp1 HG01168.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.1514+2188_1514+218 others(40): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060402 | ||||||
| chr8:100060402
|
G | GTATATAT others(33): Show |
2 | a0001c0001t0001g0036a0001c0001t0001g0256 | 2 | HG02738.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1514+2188_1514+218 others(44): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060402 | ||||||
| chr8:100060402
|
G | GTATATAT others(37): Show |
1 | a0001c0001t0001g0225 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1514+2188_1514+218 others(48): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060402 | ||||||
| chr8:100060402
|
GTA | G | 4 | a0001c0001t0001g0134a0001c0001t0001g0202a0001c0001t0001g0254others(1): Show | 4 | HG01109.hp1 HG02723.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1514+2187_1514+218 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060402 | ||||||
| chr8:100060402
|
GTATA | G | 3 | a0001c0001t0001g0198a0001c0001t0001g0215a0001c0001t0001g0294 | 3 | HG00099.hp2 HG02698.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1514+2185_1514+218 others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060402 | ||||||
| chr8:100060415
|
TATATATA others(1): Show |
T | 6 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0019others(3): Show | 6 | HG01257.hp1 HG01258.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.1514+2168_1514+217 others(12): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060415 | ||||||
| chr8:100060421
|
T | C | 3 | a0001c0001t0001g0134a0003c0022t0002g0110a0012c0023t0003g0105 | 3 | HG01109.hp1 HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1514+2170A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060421 | ||||||
| chr8:100060421
|
T | TAC | 5 | a0002c0002t0001g0085a0003c0005t0001g0061a0003c0005t0001g0106others(2): Show | 5 | HG02965.hp2 HG03225.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1514+2168_1514+216 others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060421 | ||||||
| chr8:100060421
|
T | TATAC | 10 | a0001c0001t0001g0170a0002c0002t0001g0058a0002c0002t0001g0081others(7): Show | 10 | HG00558.hp2 HG01081.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.1514+2169_1514+217 others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060421 | ||||||
| chr8:100060421
|
T | TATATAC | 14 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0086others(11): Show | 14 | HG00673.hp2 HG01943.hp2 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.1514+2169_1514+217 others(10): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060421 | ||||||
| chr8:100060421
|
T | TATATATA others(1): Show |
3 | a0002c0002t0001g0096a0010c0015t0001g0117a0014c0018t0001g0148 | 3 | HG03540.hp1 NA18991.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1514+2169_1514+217 others(12): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060421 | ||||||
| chr8:100060421
|
T | TATATATA others(3): Show |
1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1514+2169_1514+217 others(14): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060421 | ||||||
| chr8:100060421
|
T | TATATATA others(9): Show |
2 | a0001c0003t0001g0064a0001c0012t0001g0131 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1514+2169_1514+217 others(20): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060421 | ||||||
| chr8:100060421
|
T | TATATATA others(15): Show |
1 | a0001c0001t0001g0004 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1514+2169_1514+217 others(26): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060421 | ||||||
| chr8:100060421
|
T | TATATATA others(11): Show |
5 | a0001c0001t0001g0104a0001c0004t0002g0062a0001c0012t0001g0112others(2): Show | 5 | HG02145.hp2 HG02895.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1514+2169_1514+217 others(22): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060421 | ||||||
| chr8:100060421
|
T | TATATATA others(13): Show |
3 | a0001c0001t0001g0103a0001c0004t0002g0063a0006c0007t0001g0113 | 3 | HG01884.hp2 HG02630.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1514+2169_1514+217 others(24): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060421 | ||||||
| chr8:100060421
|
T | TATATATA others(17): Show |
6 | a0001c0001t0001g0041a0001c0001t0001g0158a0001c0001t0001g0207others(3): Show | 6 | HG00099.hp1 HG03831.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.1514+2169_1514+217 others(28): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060421 | ||||||
| chr8:100060421
|
T | TATATATA others(19): Show |
2 | a0001c0001t0001g0048a0001c0001t0001g0049 | 2 | NA18954.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1514+2169_1514+217 others(30): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060421 | ||||||
| chr8:100060421
|
T | TATATATA others(21): Show |
1 | a0001c0001t0001g0099 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1514+2169_1514+217 others(32): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060421 | ||||||
| chr8:100060421
|
T | TATATATA others(21): Show |
4 | a0001c0001t0001g0029a0001c0001t0001g0135a0001c0001t0001g0162others(1): Show | 4 | HG00408.hp1 HG02683.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.1514+2169_1514+217 others(32): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060421 | ||||||
| chr8:100060421
|
T | TATATATA others(23): Show |
2 | a0001c0001t0001g0228a0007c0010t0001g0171 | 2 | HG02683.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1514+2169_1514+217 others(34): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060421 | ||||||
| chr8:100060421
|
T | TATATATA others(25): Show |
2 | a0001c0001t0001g0220a0001c0001t0001g0295 | 2 | HG02738.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1514+2169_1514+217 others(36): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060421 | ||||||
| chr8:100060421
|
T | TATATATA others(27): Show |
2 | a0001c0001t0001g0188a0001c0001t0001g0192 | 2 | HG02300.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1514+2169_1514+217 others(38): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060421 | ||||||
| chr8:100060421
|
T | TATATATA others(29): Show |
5 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0190others(2): Show | 5 | HG01258.hp1 HG03927.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.1514+2169_1514+217 others(40): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060421 | ||||||
| chr8:100060421
|
T | TATATATA others(33): Show |
1 | a0001c0001t0001g0221 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1514+2169_1514+217 others(44): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060421 | ||||||
| chr8:100060423
|
C | T | 2 | a0001c0001t0001g0145a0009c0014t0001g0146 | 2 | HG03654.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1514+2168G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060423 | ||||||
| chr8:100060425
|
C | T | 2 | a0001c0001t0001g0145a0009c0014t0001g0146 | 2 | HG03654.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1514+2166G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060425 | ||||||
| chr8:100060427
|
C | T | 1 | a0002c0011t0001g0147 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1514+2164G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060427 | ||||||
| chr8:100060429
|
C | T | 1 | a0002c0011t0001g0147 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1514+2162G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060429 | ||||||
| chr8:100060553
|
C | A | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+2038G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060553 | ||||||
| chr8:100060626
|
T | A | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1965A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060626 | ||||||
| chr8:100060641
|
A | C | 1 | a0001c0001t0001g0215 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1514+1950T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060641 | ||||||
| chr8:100060653
|
T | TCAAAGAA others(17): Show |
1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1937_1514+193 others(28): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060653 | ||||||
| chr8:100060868
|
T | G | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1723A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060868 | ||||||
| chr8:100060871
|
G | T | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1720C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060871 | ||||||
| chr8:100060953
|
C | A | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1638G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060953 | ||||||
| chr8:100060956
|
G | A | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1635C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060956 | ||||||
| chr8:100060957
|
T | G | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1634A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060957 | ||||||
| chr8:100060975
|
G | T | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1616C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060975 | ||||||
| chr8:100060981
|
T | A | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1610A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060981 | ||||||
| chr8:100060982
|
C | T | 2 | a0010c0015t0001g0117a0011c0016t0001g0132 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1514+1609G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060982 | ||||||
| chr8:100060984
|
A | C | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1607T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060984 | ||||||
| chr8:100060987
|
A | T | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1604T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060987 | ||||||
| chr8:100060990
|
A | T | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1601T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060990 | ||||||
| chr8:100060993
|
G | T | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1598C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060993 | ||||||
| chr8:100060994
|
A | G | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1597T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060994 | ||||||
| chr8:100060997
|
G | C | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1594C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060997 | ||||||
| chr8:100060998
|
C | T | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1593G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060998 | ||||||
| chr8:100060999
|
A | T | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1592T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100060999 | ||||||
| chr8:100061007
|
G | A | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1584C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061007 | ||||||
| chr8:100061024
|
T | A | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1567A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061024 | ||||||
| chr8:100061038
|
A | T | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1553T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061038 | ||||||
| chr8:100061041
|
A | G | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1550T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061041 | ||||||
| chr8:100061047
|
C | T | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1544G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061047 | ||||||
| chr8:100061054
|
A | C | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1537T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061054 | ||||||
| chr8:100061062
|
G | T | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1529C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061062 | ||||||
| chr8:100061086
|
A | T | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1505T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061086 | ||||||
| chr8:100061087
|
T | G | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1504A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061087 | ||||||
| chr8:100061096
|
G | T | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1495C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061096 | ||||||
| chr8:100061195
|
C | G | 11 | a0001c0001t0001g0139a0001c0001t0001g0157a0001c0001t0001g0179others(8): Show | 11 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(8): Show |
intron_variant | MODIFIER | c.1514+1396G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061195 | ||||||
| chr8:100061196
|
T | G | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1395A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061196 | ||||||
| chr8:100061198
|
T | A | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1393A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061198 | ||||||
| chr8:100061199
|
A | G | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1392T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061199 | ||||||
| chr8:100061206
|
A | T | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1385T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061206 | ||||||
| chr8:100061207
|
T | A | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+1384A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061207 | ||||||
| chr8:100061233
|
C | T | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1514+1358G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061233 | ||||||
| chr8:100061413
|
A | G | 16 | a0003c0005t0001g0002a0003c0005t0001g0057a0003c0005t0001g0059others(13): Show | 17 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.1514+1178T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061413 | ||||||
| chr8:100061781
|
G | C | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+810C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061781 | ||||||
| chr8:100061785
|
T | G | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+806A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061785 | ||||||
| chr8:100061787
|
C | A | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+804G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061787 | ||||||
| chr8:100061788
|
C | A | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+803G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061788 | ||||||
| chr8:100061791
|
T | C | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+800A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061791 | ||||||
| chr8:100061795
|
G | A | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+796C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061795 | ||||||
| chr8:100061796
|
G | T | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+795C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061796 | ||||||
| chr8:100061808
|
A | T | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+783T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061808 | ||||||
| chr8:100061809
|
A | G | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+782T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061809 | ||||||
| chr8:100061812
|
A | T | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+779T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061812 | ||||||
| chr8:100061831
|
T | A | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+760A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061831 | ||||||
| chr8:100061832
|
A | C | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+759T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061832 | ||||||
| chr8:100061835
|
G | T | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+756C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061835 | ||||||
| chr8:100061846
|
G | A | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+745C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061846 | ||||||
| chr8:100061849
|
T | G | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+742A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061849 | ||||||
| chr8:100061851
|
T | TCAATCTG others(4): Show |
1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+739_1514+740i others(13): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061851 | ||||||
| chr8:100061852
|
G | C | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+739C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061852 | ||||||
| chr8:100061853
|
T | A | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+738A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061853 | ||||||
| chr8:100061857
|
T | C | 1 | a0001c0009t0001g0100 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1514+734A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061857 | ||||||
| chr8:100061865
|
C | T | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+726G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061865 | ||||||
| chr8:100061866
|
T | G | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+725A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061866 | ||||||
| chr8:100061917
|
A | C | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+674T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100061917 | ||||||
| chr8:100062013
|
T | A | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+578A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100062013 | ||||||
| chr8:100062014
|
G | T | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+577C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100062014 | ||||||
| chr8:100062024
|
A | C | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+567T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100062024 | ||||||
| chr8:100062025
|
T | C | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+566A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100062025 | ||||||
| chr8:100062028
|
T | C | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+563A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100062028 | ||||||
| chr8:100062031
|
G | T | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+560C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100062031 | ||||||
| chr8:100062094
|
T | G | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+497A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100062094 | ||||||
| chr8:100062097
|
T | A | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+494A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100062097 | ||||||
| chr8:100062154
|
G | T | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+437C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100062154 | ||||||
| chr8:100062238
|
C | T | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+353G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100062238 | ||||||
| chr8:100062241
|
A | C | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+350T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100062241 | ||||||
| chr8:100062287
|
C | A | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+304G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100062287 | ||||||
| chr8:100062304
|
G | A | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+287C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100062304 | ||||||
| chr8:100062324
|
A | T | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+267T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100062324 | ||||||
| chr8:100062338
|
T | A | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+253A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100062338 | ||||||
| chr8:100062352
|
A | T | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+239T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100062352 | ||||||
| chr8:100062361
|
A | C | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+230T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100062361 | ||||||
| chr8:100062362
|
T | C | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+229A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100062362 | ||||||
| chr8:100062363
|
G | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0283 | 2 | HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1514+228C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100062363 | ||||||
| chr8:100062365
|
T | C | 127 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0019others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.1514+226A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100062365 | ||||||
| chr8:100062376
|
AAAAGGCA others(3): Show |
A | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+205_1514+214d others(12): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100062376 | ||||||
| chr8:100062388
|
A | T | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+203T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100062388 | ||||||
| chr8:100062398
|
C | G | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+193G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100062398 | ||||||
| chr8:100062400
|
A | G | 162 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0008others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.1514+191T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100062400 | ||||||
| chr8:100062400
|
A | T | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+191T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100062400 | ||||||
| chr8:100062413
|
T | G | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+178A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100062413 | ||||||
| chr8:100062414
|
T | A | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+177A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100062414 | ||||||
| chr8:100062417
|
A | C | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+174T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100062417 | ||||||
| chr8:100062421
|
CACCCAAA others(3): Show |
C | 1 | a0014c0018t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1514+160_1514+169d others(12): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100062421 | ||||||
| chr8:100062436
|
A | G | 1 | a0001c0003t0001g0009 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1514+155T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100062436 | ||||||
| chr8:100062526
|
A | G | 2 | a0001c0012t0001g0112a0001c0012t0001g0131 | 2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1514+65T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 9/27 | chr8 | 100062526 | ||||||
| chr8:100062769
|
T | A | 1 | a0010c0015t0001g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1353-17A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 8/27 | chr8 | 100062769 | ||||||
| chr8:100062890
|
T | G | 1 | a0010c0015t0001g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1353-138A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 8/27 | chr8 | 100062890 | ||||||
| chr8:100062996
|
T | A | 1 | a0001c0001t0001g0293 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1353-244A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 8/27 | chr8 | 100062996 | ||||||
| chr8:100063052
|
C | G | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1353-300G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 8/27 | chr8 | 100063052 | ||||||
| chr8:100063189
|
C | T | 2 | a0001c0001t0001g0282a0001c0001t0001g0285 | 2 | HG02027.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.1352+227G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 8/27 | chr8 | 100063189 | ||||||
| chr8:100064195
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.725-152G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 7/27 | chr8 | 100064195 | ||||||
| chr8:100064490
|
GA | G | 8 | a0003c0005t0001g0002a0003c0005t0001g0061a0003c0005t0001g0069others(5): Show | 9 | HG02486.hp1 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.725-448delT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 7/27 | chr8 | 100064490 | ||||||
| chr8:100064636
|
A | T | 167 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0008others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.725-593T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 7/27 | chr8 | 100064636 | ||||||
| chr8:100064664
|
G | T | 9 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(6): Show | 9 | NA18954.hp2 NA18955.hp1 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.725-621C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 7/27 | chr8 | 100064664 | ||||||
| chr8:100064679
|
A | G | 163 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0008others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.725-636T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 7/27 | chr8 | 100064679 | ||||||
| chr8:100064718
|
G | A | 1 | a0002c0011t0001g0147 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.725-675C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 7/27 | chr8 | 100064718 | ||||||
| chr8:100064724
|
G | A | 2 | a0001c0001t0004g0142a0013c0020t0001g0279 | 2 | HG01175.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.725-681C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 7/27 | chr8 | 100064724 | ||||||
| chr8:100064882
|
C | T | 2 | a0001c0012t0001g0112a0001c0012t0001g0131 | 2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.725-839G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 7/27 | chr8 | 100064882 | ||||||
| chr8:100064923
|
C | T | 2 | a0010c0015t0001g0117a0011c0016t0001g0132 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.725-880G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 7/27 | chr8 | 100064923 | ||||||
| chr8:100065057
|
C | A | 1 | a0001c0001t0001g0097 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.725-1014G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 7/27 | chr8 | 100065057 | ||||||
| chr8:100065241
|
TAC | T | 13 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0149others(10): Show | 13 | HG00558.hp2 HG00673.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.724+924_724+925del others(2): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 7/27 | chr8 | 100065241 | ||||||
| chr8:100065246
|
T | C | 1 | a0002c0002t0001g0085 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.724+921A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 7/27 | chr8 | 100065246 | ||||||
| chr8:100065319
|
C | T | 1 | a0001c0001t0001g0226 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.724+848G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 7/27 | chr8 | 100065319 | ||||||
| chr8:100065410
|
A | G | 3 | a0001c0001t0001g0067a0001c0001t0003g0003a0001c0003t0001g0005 | 3 | HG01243.hp2 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.724+757T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 7/27 | chr8 | 100065410 | ||||||
| chr8:100065667
|
T | G | 1 | a0003c0005t0001g0095 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.724+500A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 7/27 | chr8 | 100065667 | ||||||
| chr8:100065731
|
T | A | 27 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(24): Show | 27 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.724+436A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 7/27 | chr8 | 100065731 | ||||||
| chr8:100065739
|
T | A | 2 | a0001c0001t0001g0256a0001c0001t0001g0258 | 2 | HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.724+428A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 7/27 | chr8 | 100065739 | ||||||
| chr8:100065860
|
C | G | 27 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(24): Show | 27 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.724+307G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 7/27 | chr8 | 100065860 | ||||||
| chr8:100066005
|
T | C | 1 | a0003c0005t0001g0059 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.724+162A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 7/27 | chr8 | 100066005 | ||||||
| chr8:100066123
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.724+44G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 7/27 | chr8 | 100066123 | ||||||
| chr8:100066375
|
A | G | 1 | a0001c0004t0002g0124 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.595-79T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100066375 | ||||||
| chr8:100066819
|
T | C | 1 | a0001c0001t0001g0024 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.595-523A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100066819 | ||||||
| chr8:100066823
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.595-527G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100066823 | ||||||
| chr8:100066910
|
A | G | 2 | a0001c0004t0002g0121a0001c0004t0002g0122 | 2 | HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.595-614T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100066910 | ||||||
| chr8:100067250
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.595-954G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100067250 | ||||||
| chr8:100067565
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.595-1269C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100067565 | ||||||
| chr8:100067621
|
A | AT | 21 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0042others(18): Show | 21 | HG00408.hp1 HG00438.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.595-1326dupA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100067621 | ||||||
| chr8:100067621
|
AT | A | 82 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(79): Show | 83 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.595-1326delA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100067621 | ||||||
| chr8:100067621
|
ATT | A | 6 | a0001c0001t0001g0099a0001c0001t0001g0103a0001c0001t0001g0104others(3): Show | 6 | HG01884.hp2 HG02630.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.595-1327_595-1326d others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100067621 | ||||||
| chr8:100067621
|
ATTTTTTT others(4): Show |
A | 3 | a0002c0002t0001g0083a0002c0002t0001g0084a0002c0002t0001g0085 | 3 | NA18944.hp2 NA18983.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.595-1336_595-1326d others(13): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100067621 | ||||||
| chr8:100067749
|
C | G | 1 | a0001c0001t0001g0030 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.595-1453G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100067749 | ||||||
| chr8:100067750
|
G | A | 3 | a0001c0001t0001g0284a0001c0009t0001g0100a0001c0009t0001g0101 | 3 | HG02486.hp2 HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.595-1454C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100067750 | ||||||
| chr8:100067903
|
G | A | 160 | a0000c0021t0001g0150a0001c0001t0001g0008a0001c0001t0001g0018others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.595-1607C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100067903 | ||||||
| chr8:100068210
|
C | A | 1 | a0001c0003t0001g0130 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.595-1914G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100068210 | ||||||
| chr8:100068213
|
C | T | 1 | a0001c0012t0001g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.595-1917G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100068213 | ||||||
| chr8:100068554
|
TC | T | 3 | a0001c0001t0001g0067a0001c0003t0001g0005a0003c0005t0001g0068 | 3 | HG02559.hp2 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.595-2259delG | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100068554 | ||||||
| chr8:100068669
|
C | T | 28 | a0000c0021t0001g0150a0001c0001t0001g0098a0002c0002t0001g0033others(25): Show | 28 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.595-2373G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100068669 | ||||||
| chr8:100068835
|
G | C | 3 | a0002c0002t0001g0153a0002c0002t0001g0155a0002c0002t0001g0156 | 3 | HG00558.hp2 HG02040.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.594+2534C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100068835 | ||||||
| chr8:100068912
|
G | C | 2 | a0010c0015t0001g0117a0011c0016t0001g0132 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.594+2457C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100068912 | ||||||
| chr8:100068934
|
CA | C | 207 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.594+2434delT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100068934 | ||||||
| chr8:100068942
|
A | T | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.594+2427T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100068942 | ||||||
| chr8:100068957
|
G | GA | 224 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(221): Show | 225 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.594+2411dupT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100068957 | ||||||
| chr8:100069188
|
A | G | 5 | a0001c0001t0001g0067a0001c0001t0001g0134a0001c0001t0003g0003others(2): Show | 5 | HG01109.hp1 HG01243.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.594+2181T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100069188 | ||||||
| chr8:100069352
|
T | C | 4 | a0001c0001t0001g0103a0006c0007t0001g0113a0006c0007t0001g0125others(1): Show | 4 | HG01884.hp2 HG02630.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+2017A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100069352 | ||||||
| chr8:100069470
|
A | T | 3 | a0003c0005t0001g0069a0003c0005t0001g0107a0003c0005t0001g0108 | 3 | HG02717.hp1 HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.594+1899T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100069470 | ||||||
| chr8:100069699
|
T | C | 1 | a0001c0001t0001g0024 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.594+1670A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100069699 | ||||||
| chr8:100069828
|
G | A | 1 | a0010c0015t0001g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.594+1541C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100069828 | ||||||
| chr8:100069971
|
T | G | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.594+1398A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100069971 | ||||||
| chr8:100069977
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.594+1392C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100069977 | ||||||
| chr8:100070027
|
C | CA | 95 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 95 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.594+1341dupT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100070027 | ||||||
| chr8:100070027
|
C | CAA | 12 | a0000c0019t0001g0248a0001c0001t0001g0042a0001c0001t0001g0043others(9): Show | 12 | HG00673.hp1 HG00735.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.594+1340_594+1341d others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100070027 | ||||||
| chr8:100070044
|
A | C | 3 | a0001c0001t0001g0268a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01071.hp1 HG01433.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.594+1325T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100070044 | ||||||
| chr8:100070048
|
AC | A | 31 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0098others(28): Show | 31 | HG00673.hp2 HG01081.hp1 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.594+1320delG | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100070048 | ||||||
| chr8:100070049
|
C | A | 134 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0019others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.594+1320G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100070049 | ||||||
| chr8:100070054
|
C | A | 5 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0174others(2): Show | 5 | HG01261.hp2 HG02300.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.594+1315G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100070054 | ||||||
| chr8:100070383
|
G | A | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.594+986C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100070383 | ||||||
| chr8:100070426
|
T | C | 3 | a0001c0001t0001g0067a0001c0003t0001g0005a0003c0005t0001g0068 | 3 | HG02559.hp2 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.594+943A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100070426 | ||||||
| chr8:100070812
|
T | C | 5 | a0001c0001t0001g0067a0001c0001t0001g0134a0001c0001t0003g0003others(2): Show | 5 | HG01109.hp1 HG01243.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.594+557A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100070812 | ||||||
| chr8:100070837
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.594+532C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100070837 | ||||||
| chr8:100070911
|
T | C | 1 | a0016c0025t0001g0307 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.594+458A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100070911 | ||||||
| chr8:100070924
|
T | C | 136 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0018others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.594+445A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100070924 | ||||||
| chr8:100071020
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.594+349G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100071020 | ||||||
| chr8:100071049
|
G | A | 5 | a0001c0001t0001g0067a0001c0001t0001g0134a0001c0001t0003g0003others(2): Show | 5 | HG01109.hp1 HG01243.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.594+320C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100071049 | ||||||
| chr8:100071086
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.594+283G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100071086 | ||||||
| chr8:100071212
|
C | T | 2 | a0001c0009t0001g0100a0001c0009t0001g0101 | 2 | HG02486.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.594+157G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 6/27 | chr8 | 100071212 | ||||||
| chr8:100071784
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.426-247T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 5/27 | chr8 | 100071784 | ||||||
| chr8:100071850
|
T | C | 2 | a0001c0012t0001g0112a0001c0012t0001g0131 | 2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.425+295A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 5/27 | chr8 | 100071850 | ||||||
| chr8:100071897
|
T | C | 2 | a0001c0001t0001g0268a0001c0001t0001g0273 | 2 | HG01433.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.425+248A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 5/27 | chr8 | 100071897 | ||||||
| chr8:100071995
|
G | A | 2 | a0010c0015t0001g0117a0011c0016t0001g0132 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.425+150C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 5/27 | chr8 | 100071995 | ||||||
| chr8:100072078
|
G | C | 1 | a0001c0001t0001g0099 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.425+67C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 5/27 | chr8 | 100072078 | ||||||
| chr8:100072419
|
GT | G | 139 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0022others(136): Show | 139 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.340-190delA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100072419 | ||||||
| chr8:100072828
|
C | T | 141 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0022others(138): Show | 141 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.340-598G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100072828 | ||||||
| chr8:100073261
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.340-1031T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100073261 | ||||||
| chr8:100073429
|
CA | C | 199 | a0000c0019t0001g0248a0001c0001t0001g0004a0001c0001t0001g0008others(196): Show | 201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.340-1200delT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100073429 | ||||||
| chr8:100073432
|
AAAAAAAA others(3): Show |
A | 26 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(23): Show | 26 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.340-1212_340-1203d others(12): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100073432 | ||||||
| chr8:100073434
|
A | C | 3 | a0001c0001t0001g0237a0001c0001t0001g0254a0001c0001t0001g0273 | 3 | HG06807.hp1 NA18984.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.340-1204T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100073434 | ||||||
| chr8:100073435
|
A | C | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.340-1205T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100073435 | ||||||
| chr8:100073450
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.340-1220T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100073450 | ||||||
| chr8:100073472
|
C | G | 4 | a0001c0001t0001g0067a0001c0001t0003g0003a0001c0003t0001g0005others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.340-1242G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100073472 | ||||||
| chr8:100073550
|
G | A | 139 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0022others(136): Show | 139 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.340-1320C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100073550 | ||||||
| chr8:100073594
|
T | C | 1 | a0010c0015t0001g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.340-1364A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100073594 | ||||||
| chr8:100073649
|
C | T | 2 | a0001c0001t0001g0019a0001c0001t0001g0020 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.340-1419G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100073649 | ||||||
| chr8:100074011
|
C | T | 28 | a0000c0021t0001g0150a0001c0001t0001g0098a0002c0002t0001g0033others(25): Show | 28 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.340-1781G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100074011 | ||||||
| chr8:100074211
|
T | C | 2 | a0001c0001t0001g0255a0001c0001t0001g0261 | 2 | HG02040.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.340-1981A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100074211 | ||||||
| chr8:100074242
|
C | T | 3 | a0001c0001t0001g0284a0001c0009t0001g0100a0001c0009t0001g0101 | 3 | HG02486.hp2 HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.340-2012G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100074242 | ||||||
| chr8:100074414
|
C | G | 102 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0034others(99): Show | 102 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.340-2184G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100074414 | ||||||
| chr8:100074697
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.340-2467A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100074697 | ||||||
| chr8:100074749
|
G | GT | 11 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0103others(8): Show | 11 | HG01884.hp2 HG02145.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.340-2520dupA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100074749 | ||||||
| chr8:100074753
|
T | G | 124 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0019others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.340-2523A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100074753 | ||||||
| chr8:100074799
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.340-2569C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100074799 | ||||||
| chr8:100074828
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.340-2598G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100074828 | ||||||
| chr8:100074837
|
G | A | 3 | a0001c0001t0001g0284a0001c0009t0001g0100a0001c0009t0001g0101 | 3 | HG02486.hp2 HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.340-2607C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100074837 | ||||||
| chr8:100074892
|
C | T | 2 | a0001c0012t0001g0112a0001c0012t0001g0131 | 2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.340-2662G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100074892 | ||||||
| chr8:100074928
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.340-2698G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100074928 | ||||||
| chr8:100074929
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.340-2699C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100074929 | ||||||
| chr8:100075061
|
C | T | 3 | a0001c0001t0001g0284a0001c0009t0001g0100a0001c0009t0001g0101 | 3 | HG02486.hp2 HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.340-2831G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100075061 | ||||||
| chr8:100075121
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.340-2891G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100075121 | ||||||
| chr8:100075122
|
A | G | 164 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0008others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.340-2892T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100075122 | ||||||
| chr8:100075145
|
A | C | 1 | a0001c0001t0001g0268 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.340-2915T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100075145 | ||||||
| chr8:100075185
|
A | C | 7 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0103others(4): Show | 7 | HG01884.hp2 HG02630.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.340-2955T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100075185 | ||||||
| chr8:100075327
|
A | G | 1 | a0001c0001t0003g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.340-3097T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100075327 | ||||||
| chr8:100075455
|
A | G | 15 | a0003c0005t0001g0002a0003c0005t0001g0057a0003c0005t0001g0059others(12): Show | 16 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.340-3225T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100075455 | ||||||
| chr8:100075560
|
G | C | 1 | a0001c0001t0001g0163 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.340-3330C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100075560 | ||||||
| chr8:100075688
|
T | C | 1 | a0001c0001t0001g0297 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.340-3458A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100075688 | ||||||
| chr8:100075747
|
G | C | 1 | a0001c0004t0002g0120 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.340-3517C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100075747 | ||||||
| chr8:100076714
|
C | T | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.339+3420G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100076714 | ||||||
| chr8:100076731
|
C | G | 141 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0022others(138): Show | 141 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.339+3403G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100076731 | ||||||
| chr8:100076761
|
G | A | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG02683.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.339+3373C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100076761 | ||||||
| chr8:100076767
|
C | T | 2 | a0010c0015t0001g0117a0011c0016t0001g0132 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.339+3367G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100076767 | ||||||
| chr8:100076791
|
G | A | 1 | a0001c0001t0001g0225 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.339+3343C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100076791 | ||||||
| chr8:100076980
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.339+3154C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100076980 | ||||||
| chr8:100077071
|
AT | A | 6 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0019others(3): Show | 6 | HG01257.hp1 HG01258.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.339+3062delA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100077071 | ||||||
| chr8:100077083
|
T | G | 2 | a0010c0015t0001g0117a0011c0016t0001g0132 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.339+3051A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100077083 | ||||||
| chr8:100077094
|
T | C | 1 | a0002c0002t0001g0058 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.339+3040A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100077094 | ||||||
| chr8:100077183
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.339+2951A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100077183 | ||||||
| chr8:100077539
|
T | C | 1 | a0001c0001t0001g0201 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.339+2595A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100077539 | ||||||
| chr8:100077633
|
C | T | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.339+2501G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100077633 | ||||||
| chr8:100077825
|
C | A | 2 | a0001c0004t0002g0121a0001c0004t0002g0122 | 2 | HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.339+2309G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100077825 | ||||||
| chr8:100077862
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.339+2272A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100077862 | ||||||
| chr8:100077982
|
T | C | 5 | a0001c0001t0001g0232a0001c0001t0001g0234a0001c0001t0001g0235others(2): Show | 5 | NA18960.hp2 NA18963.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.339+2152A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100077982 | ||||||
| chr8:100078138
|
C | T | 28 | a0000c0021t0001g0150a0001c0001t0001g0098a0002c0002t0001g0033others(25): Show | 28 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.339+1996G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100078138 | ||||||
| chr8:100078160
|
T | A | 6 | a0001c0001t0001g0067a0001c0001t0003g0003a0001c0003t0001g0005others(3): Show | 6 | HG01243.hp2 HG02559.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.339+1974A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100078160 | ||||||
| chr8:100078189
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.339+1945G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100078189 | ||||||
| chr8:100078198
|
C | T | 4 | a0001c0001t0001g0231a0001c0001t0001g0240a0001c0001t0001g0260others(1): Show | 4 | HG00544.hp2 NA18979.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.339+1936G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100078198 | ||||||
| chr8:100078259
|
A | G | 142 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0022others(139): Show | 142 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.339+1875T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100078259 | ||||||
| chr8:100078517
|
T | A | 1 | a0009c0014t0001g0146 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.339+1617A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100078517 | ||||||
| chr8:100078575
|
A | G | 1 | a0005c0006t0001g0092 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.339+1559T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100078575 | ||||||
| chr8:100078823
|
C | T | 140 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0022others(137): Show | 140 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.339+1311G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100078823 | ||||||
| chr8:100078838
|
A | T | 1 | a0001c0001t0001g0218 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.339+1296T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100078838 | ||||||
| chr8:100079061
|
C | T | 142 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0022others(139): Show | 142 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.339+1073G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100079061 | ||||||
| chr8:100079341
|
T | A | 58 | a0000c0019t0001g0248a0001c0001t0001g0008a0001c0001t0001g0018others(55): Show | 58 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.339+793A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100079341 | ||||||
| chr8:100079701
|
C | A | 1 | a0001c0001t0001g0157 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.339+433G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100079701 | ||||||
| chr8:100079791
|
T | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0103others(5): Show | 8 | HG01884.hp2 HG02630.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.339+343A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100079791 | ||||||
| chr8:100079969
|
T | G | 1 | a0002c0002t0001g0259 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.339+165A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 4/27 | chr8 | 100079969 | ||||||
| chr8:100080735
|
C | T | 4 | a0001c0001t0001g0067a0001c0001t0003g0003a0001c0003t0001g0005others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-380G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100080735 | ||||||
| chr8:100080982
|
G | A | 2 | a0010c0015t0001g0117a0011c0016t0001g0132 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.118-627C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100080982 | ||||||
| chr8:100081024
|
T | C | 202 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.118-669A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100081024 | ||||||
| chr8:100081360
|
A | ATG | 27 | a0000c0021t0001g0150a0002c0002t0001g0033a0002c0002t0001g0058others(24): Show | 27 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.118-1007_118-1006d others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100081360 | ||||||
| chr8:100081362
|
G | GTA | 13 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0021others(10): Show | 13 | HG01123.hp2 HG01884.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.118-1009_118-1008d others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100081362 | ||||||
| chr8:100081362
|
G | GTATA | 52 | a0000c0019t0001g0248a0001c0001t0001g0022a0001c0001t0001g0030others(49): Show | 52 | HG00099.hp1 HG00621.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.118-1011_118-1008d others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100081362 | ||||||
| chr8:100081362
|
G | GTATATA | 84 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0001g0036others(81): Show | 84 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.118-1013_118-1008d others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100081362 | ||||||
| chr8:100081362
|
G | GTATATAT others(1): Show |
19 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0138others(16): Show | 19 | HG00733.hp2 HG00735.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.118-1015_118-1008d others(10): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100081362 | ||||||
| chr8:100081362
|
G | GTATATAT others(3): Show |
3 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0209 | 3 | NA18954.hp1 NA18983.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.118-1017_118-1008d others(12): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100081362 | ||||||
| chr8:100081362
|
GTA | G | 3 | a0001c0001t0003g0003a0001c0012t0001g0112a0001c0012t0001g0131 | 3 | HG01243.hp2 HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.118-1009_118-1008d others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100081362 | ||||||
| chr8:100081373
|
T | TATAA | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020 | 3 | HG01257.hp1 HG01258.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.118-1019_118-1018i others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100081373 | ||||||
| chr8:100081803
|
A | G | 202 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.118-1448T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100081803 | ||||||
| chr8:100081807
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.118-1452C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100081807 | ||||||
| chr8:100081838
|
A | G | 200 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.118-1483T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100081838 | ||||||
| chr8:100081909
|
C | CT | 9 | a0001c0001t0001g0176a0001c0001t0001g0199a0001c0001t0001g0202others(6): Show | 9 | HG02486.hp2 HG02572.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.118-1555dupA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100081909 | ||||||
| chr8:100081909
|
CTTTTTTT | C | 63 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0037others(60): Show | 63 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.118-1561_118-1555d others(9): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100081909 | ||||||
| chr8:100081937
|
C | T | 2 | a0001c0012t0001g0112a0001c0012t0001g0131 | 2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.118-1582G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100081937 | ||||||
| chr8:100081982
|
C | A | 202 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.118-1627G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100081982 | ||||||
| chr8:100081987
|
A | G | 1 | a0001c0001t0001g0282 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.118-1632T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100081987 | ||||||
| chr8:100082151
|
C | T | 1 | a0002c0002t0001g0086 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.118-1796G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100082151 | ||||||
| chr8:100082174
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.118-1819A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100082174 | ||||||
| chr8:100082346
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.118-1991A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100082346 | ||||||
| chr8:100082469
|
A | G | 2 | a0001c0012t0001g0112a0001c0012t0001g0131 | 2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.118-2114T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100082469 | ||||||
| chr8:100082751
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.118-2396A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100082751 | ||||||
| chr8:100082900
|
T | G | 124 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0019others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.118-2545A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100082900 | ||||||
| chr8:100082913
|
G | A | 197 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.118-2558C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100082913 | ||||||
| chr8:100082983
|
GATAACAT others(3): Show |
G | 2 | a0010c0015t0001g0117a0011c0016t0001g0132 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.118-2638_118-2629d others(12): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100082983 | ||||||
| chr8:100082998
|
C | T | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.118-2643G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100082998 | ||||||
| chr8:100083089
|
T | C | 3 | a0001c0001t0001g0067a0001c0003t0001g0005a0003c0005t0001g0068 | 3 | HG02559.hp2 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.118-2734A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100083089 | ||||||
| chr8:100083162
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.118-2807G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100083162 | ||||||
| chr8:100083331
|
C | T | 102 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0034others(99): Show | 102 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.118-2976G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100083331 | ||||||
| chr8:100083379
|
T | G | 1 | a0001c0012t0001g0131 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.118-3024A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100083379 | ||||||
| chr8:100083417
|
G | C | 2 | a0001c0004t0002g0121a0001c0004t0002g0122 | 2 | HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.118-3062C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100083417 | ||||||
| chr8:100083460
|
T | C | 1 | a0001c0001t0001g0263 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.118-3105A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100083460 | ||||||
| chr8:100083543
|
T | C | 2 | a0001c0001t0001g0290a0001c0001t0001g0292 | 2 | HG00738.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.118-3188A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100083543 | ||||||
| chr8:100083765
|
A | G | 1 | a0001c0001t0003g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.118-3410T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100083765 | ||||||
| chr8:100083830
|
CT | C | 107 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(104): Show | 107 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.118-3476delA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100083830 | ||||||
| chr8:100083830
|
CTT | C | 97 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0036others(94): Show | 97 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.118-3477_118-3476d others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100083830 | ||||||
| chr8:100083837
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.118-3482A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100083837 | ||||||
| chr8:100083861
|
T | C | 57 | a0000c0019t0001g0248a0001c0001t0001g0008a0001c0001t0001g0018others(54): Show | 57 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.118-3506A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100083861 | ||||||
| chr8:100083885
|
C | T | 3 | a0001c0001t0001g0042a0001c0001t0001g0219a0001c0024t0001g0299 | 3 | HG02109.hp2 HG02451.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.118-3530G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100083885 | ||||||
| chr8:100083958
|
T | C | 1 | a0001c0003t0001g0080 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.118-3603A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100083958 | ||||||
| chr8:100084129
|
G | C | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.118-3774C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100084129 | ||||||
| chr8:100084185
|
C | G | 1 | a0001c0001t0001g0265 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.118-3830G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100084185 | ||||||
| chr8:100084503
|
T | C | 1 | a0000c0019t0001g0248 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.118-4148A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100084503 | ||||||
| chr8:100084571
|
T | A | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.118-4216A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100084571 | ||||||
| chr8:100084781
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.118-4426G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100084781 | ||||||
| chr8:100084933
|
T | C | 4 | a0001c0001t0001g0111a0001c0001t0001g0233a0001c0001t0001g0247others(1): Show | 4 | HG01255.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-4578A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100084933 | ||||||
| chr8:100084980
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.118-4625C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100084980 | ||||||
| chr8:100085217
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.118-4862G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100085217 | ||||||
| chr8:100085543
|
T | C | 2 | a0001c0001t0001g0019a0001c0001t0001g0020 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.118-5188A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100085543 | ||||||
| chr8:100085593
|
T | G | 1 | a0001c0001t0001g0129 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.118-5238A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100085593 | ||||||
| chr8:100085937
|
A | G | 1 | a0002c0002t0001g0086 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.118-5582T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100085937 | ||||||
| chr8:100085939
|
C | T | 1 | a0001c0001t0001g0200 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.118-5584G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100085939 | ||||||
| chr8:100085943
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.118-5588T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100085943 | ||||||
| chr8:100085996
|
A | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0028 | 2 | HG02300.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.118-5641T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100085996 | ||||||
| chr8:100086233
|
G | A | 5 | a0001c0001t0001g0103a0001c0001t0001g0104a0006c0007t0001g0113others(2): Show | 5 | HG01884.hp2 HG02630.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-5878C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100086233 | ||||||
| chr8:100086311
|
G | T | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.118-5956C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100086311 | ||||||
| chr8:100086470
|
A | G | 2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.118-6115T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100086470 | ||||||
| chr8:100086657
|
G | A | 1 | a0000c0019t0001g0248 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.118-6302C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100086657 | ||||||
| chr8:100086674
|
C | T | 5 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0024others(2): Show | 5 | NA18952.hp1 NA19063.hp2 NA19068.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-6319G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100086674 | ||||||
| chr8:100086781
|
G | A | 1 | a0010c0015t0001g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.118-6426C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100086781 | ||||||
| chr8:100086989
|
G | A | 4 | a0001c0001t0001g0067a0001c0001t0003g0003a0001c0003t0001g0005others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+6458C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100086989 | ||||||
| chr8:100087288
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.117+6159G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100087288 | ||||||
| chr8:100087491
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.117+5956T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100087491 | ||||||
| chr8:100087539
|
G | T | 20 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0066others(17): Show | 20 | HG00597.hp2 HG01884.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.117+5908C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100087539 | ||||||
| chr8:100087672
|
C | T | 1 | a0002c0002t0001g0096 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.117+5775G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100087672 | ||||||
| chr8:100087839
|
C | G | 2 | a0001c0004t0002g0062a0001c0004t0002g0063 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.117+5608G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100087839 | ||||||
| chr8:100088110
|
C | A | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.117+5337G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100088110 | ||||||
| chr8:100088135
|
T | C | 1 | a0001c0001t0003g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.117+5312A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100088135 | ||||||
| chr8:100088169
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.117+5278C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100088169 | ||||||
| chr8:100088273
|
C | T | 3 | a0006c0007t0001g0113a0006c0007t0001g0125a0006c0007t0001g0126 | 3 | HG01884.hp2 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.117+5174G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100088273 | ||||||
| chr8:100088377
|
C | T | 216 | a0000c0019t0001g0248a0000c0021t0001g0150a0001c0001t0001g0004others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.117+5070G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100088377 | ||||||
| chr8:100089123
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.117+4324C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100089123 | ||||||
| chr8:100089211
|
A | AAC | 19 | a0001c0001t0001g0031a0001c0001t0001g0037a0001c0001t0001g0047others(16): Show | 19 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(16): Show |
intron_variant | MODIFIER | c.117+4234_117+4235d others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100089211 | ||||||
| chr8:100089211
|
A | AACACAC | 18 | a0001c0001t0001g0118a0001c0001t0001g0128a0001c0001t0001g0129others(15): Show | 18 | HG00733.hp1 HG00738.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.117+4230_117+4235d others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100089211 | ||||||
| chr8:100089211
|
A | AACACACA others(7): Show |
1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.117+4222_117+4235d others(16): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100089211 | ||||||
| chr8:100089419
|
G | A | 2 | a0001c0001t0001g0247a0002c0002t0001g0133 | 2 | HG01255.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.117+4028C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100089419 | ||||||
| chr8:100089628
|
G | A | 1 | a0001c0009t0001g0101 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.117+3819C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100089628 | ||||||
| chr8:100090052
|
C | T | 1 | a0010c0015t0001g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.117+3395G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100090052 | ||||||
| chr8:100090187
|
G | C | 1 | a0001c0001t0001g0201 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.117+3260C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100090187 | ||||||
| chr8:100090272
|
A | G | 2 | a0001c0001t0001g0266a0002c0002t0001g0259 | 2 | HG03710.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.117+3175T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100090272 | ||||||
| chr8:100090320
|
A | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020 | 3 | HG01257.hp1 HG01258.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.117+3127T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100090320 | ||||||
| chr8:100090381
|
G | C | 1 | a0001c0003t0001g0077 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.117+3066C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100090381 | ||||||
| chr8:100090421
|
TG | T | 60 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0090others(57): Show | 61 | HG00558.hp2 HG00673.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.117+3025delC | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100090421 | ||||||
| chr8:100090540
|
T | C | 82 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0090others(79): Show | 83 | HG00558.hp2 HG00673.hp2 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.117+2907A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100090540 | ||||||
| chr8:100090545
|
C | G | 60 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0090others(57): Show | 61 | HG00558.hp2 HG00673.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.117+2902G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100090545 | ||||||
| chr8:100090560
|
C | T | 60 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0090others(57): Show | 61 | HG00558.hp2 HG00673.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.117+2887G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100090560 | ||||||
| chr8:100090618
|
G | A | 60 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0090others(57): Show | 61 | HG00558.hp2 HG00673.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.117+2829C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100090618 | ||||||
| chr8:100090657
|
G | T | 60 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0090others(57): Show | 61 | HG00558.hp2 HG00673.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.117+2790C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100090657 | ||||||
| chr8:100090693
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.117+2754C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100090693 | ||||||
| chr8:100090901
|
T | C | 43 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0019others(40): Show | 43 | HG00099.hp1 HG00735.hp2 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.117+2546A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100090901 | ||||||
| chr8:100090903
|
G | A | 60 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0090others(57): Show | 61 | HG00558.hp2 HG00673.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.117+2544C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100090903 | ||||||
| chr8:100091081
|
T | C | 22 | a0001c0001t0001g0118a0001c0001t0001g0128a0001c0001t0001g0129others(19): Show | 22 | HG00733.hp1 HG00738.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.117+2366A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100091081 | ||||||
| chr8:100091168
|
C | T | 1 | a0002c0002t0001g0086 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.117+2279G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100091168 | ||||||
| chr8:100091292
|
TC | T | 59 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0090others(56): Show | 60 | HG00558.hp2 HG00673.hp2 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.117+2154delG | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100091292 | ||||||
| chr8:100091571
|
C | T | 222 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0008others(219): Show | 224 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.117+1876G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100091571 | ||||||
| chr8:100091697
|
C | G | 1 | a0002c0011t0001g0147 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.117+1750G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100091697 | ||||||
| chr8:100091720
|
A | C | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG02683.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.117+1727T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100091720 | ||||||
| chr8:100091786
|
T | C | 60 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0090others(57): Show | 61 | HG00558.hp2 HG00673.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.117+1661A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100091786 | ||||||
| chr8:100091974
|
G | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0102others(2): Show | 5 | HG02630.hp1 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+1473C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100091974 | ||||||
| chr8:100092065
|
CAT | C | 220 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0008others(217): Show | 222 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.117+1380_117+1381d others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100092065 | ||||||
| chr8:100092088
|
T | C | 1 | a0001c0001t0001g0164 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.117+1359A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100092088 | ||||||
| chr8:100092458
|
T | C | 1 | a0001c0001t0001g0210 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.117+989A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100092458 | ||||||
| chr8:100092746
|
C | T | 61 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0090others(58): Show | 62 | HG00558.hp2 HG00673.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.117+701G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100092746 | ||||||
| chr8:100092818
|
T | C | 3 | a0001c0001t0001g0138a0001c0001t0001g0202a0001c0001t0001g0203 | 3 | HG01109.hp2 HG01517.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.117+629A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100092818 | ||||||
| chr8:100092830
|
T | TCAATCTA others(5): Show |
1 | a0001c0001t0001g0218 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.117+605_117+616dup others(12): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100092830 | ||||||
| chr8:100093160
|
T | C | 7 | a0003c0005t0001g0002a0003c0005t0001g0106a0003c0005t0001g0107others(4): Show | 8 | HG02451.hp2 HG02486.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+287A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100093160 | ||||||
| chr8:100093274
|
T | A | 61 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0090others(58): Show | 62 | HG00558.hp2 HG00673.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.117+173A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 3/27 | chr8 | 100093274 | ||||||
| chr8:100094007
|
C | T | 61 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0090others(58): Show | 62 | HG00558.hp2 HG00673.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.55-498G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100094007 | ||||||
| chr8:100094027
|
AAAT | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0102others(2): Show | 5 | HG02630.hp1 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.55-521_55-519delAT others(1): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100094027 | ||||||
| chr8:100094100
|
G | A | 61 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0090others(58): Show | 62 | HG00558.hp2 HG00673.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.55-591C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100094100 | ||||||
| chr8:100094113
|
A | T | 1 | a0004c0008t0001g0173 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.55-604T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100094113 | ||||||
| chr8:100094117
|
A | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.55-608T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100094117 | ||||||
| chr8:100094335
|
ATATGACA others(9): Show |
A | 61 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0090others(58): Show | 62 | HG00558.hp2 HG00673.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.55-842_55-827delAT others(14): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100094335 | ||||||
| chr8:100094392
|
A | G | 1 | a0001c0003t0001g0077 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.55-883T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100094392 | ||||||
| chr8:100094435
|
A | G | 43 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0019others(40): Show | 43 | HG00099.hp1 HG00735.hp2 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.55-926T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100094435 | ||||||
| chr8:100094876
|
G | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0102others(2): Show | 5 | HG02630.hp1 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.55-1367C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100094876 | ||||||
| chr8:100094993
|
T | C | 61 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0090others(58): Show | 62 | HG00558.hp2 HG00673.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.55-1484A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100094993 | ||||||
| chr8:100095054
|
C | T | 22 | a0001c0001t0001g0118a0001c0001t0001g0128a0001c0001t0001g0129others(19): Show | 22 | HG00733.hp1 HG00738.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.55-1545G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100095054 | ||||||
| chr8:100095412
|
A | G | 61 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0090others(58): Show | 62 | HG00558.hp2 HG00673.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.55-1903T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100095412 | ||||||
| chr8:100095522
|
C | T | 61 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0090others(58): Show | 62 | HG00558.hp2 HG00673.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.55-2013G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100095522 | ||||||
| chr8:100095690
|
T | C | 1 | a0001c0004t0002g0124 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.55-2181A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100095690 | ||||||
| chr8:100095791
|
C | A | 1 | a0001c0001t0001g0230 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.55-2282G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100095791 | ||||||
| chr8:100095834
|
T | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0102others(2): Show | 5 | HG02630.hp1 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.55-2325A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100095834 | ||||||
| chr8:100095836
|
T | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0102others(2): Show | 5 | HG02630.hp1 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.55-2327A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100095836 | ||||||
| chr8:100095837
|
C | A | 6 | a0001c0001t0001g0090a0001c0001t0001g0093a0002c0002t0001g0086others(3): Show | 6 | NA18946.hp2 NA18965.hp1 NA19001.hp2 others(3): Show |
intron_variant | MODIFIER | c.55-2328G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100095837 | ||||||
| chr8:100095842
|
A | C | 61 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0090others(58): Show | 62 | HG00558.hp2 HG00673.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.55-2333T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100095842 | ||||||
| chr8:100095868
|
A | C | 7 | a0003c0005t0001g0002a0003c0005t0001g0106a0003c0005t0001g0107others(4): Show | 8 | HG02451.hp2 HG02486.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.55-2359T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100095868 | ||||||
| chr8:100095916
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.55-2407T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100095916 | ||||||
| chr8:100096027
|
T | C | 2 | a0001c0001t0001g0066a0001c0001t0001g0283 | 2 | HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.55-2518A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100096027 | ||||||
| chr8:100096085
|
G | C | 1 | a0001c0012t0001g0131 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.55-2576C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100096085 | ||||||
| chr8:100096599
|
G | A | 20 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0048others(17): Show | 20 | HG02145.hp1 HG02280.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.55-3090C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100096599 | ||||||
| chr8:100096607
|
A | AT | 170 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0016others(167): Show | 172 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.55-3099dupA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100096607 | ||||||
| chr8:100096607
|
A | ATT | 20 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0165others(17): Show | 20 | HG00738.hp1 HG01175.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.55-3100_55-3099dup others(2): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100096607 | ||||||
| chr8:100096670
|
A | AT | 24 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0019others(21): Show | 24 | HG00099.hp1 HG00735.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.55-3162_55-3161ins others(1): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100096670 | ||||||
| chr8:100096670
|
A | T | 20 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0047others(17): Show | 20 | HG01934.hp1 HG02145.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.55-3161T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100096670 | ||||||
| chr8:100096671
|
A | T | 137 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0019others(134): Show | 138 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.55-3162T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100096671 | ||||||
| chr8:100096671
|
AT | A | 80 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0026others(77): Show | 81 | HG00558.hp2 HG00673.hp2 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.55-3163delA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100096671 | ||||||
| chr8:100096732
|
C | T | 1 | a0005c0006t0001g0091 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.55-3223G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100096732 | ||||||
| chr8:100096758
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0093 | 2 | NA19010.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.55-3249G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100096758 | ||||||
| chr8:100096848
|
G | A | 1 | a0001c0001t0001g0285 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.55-3339C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100096848 | ||||||
| chr8:100097008
|
A | G | 22 | a0001c0001t0001g0118a0001c0001t0001g0128a0001c0001t0001g0129others(19): Show | 22 | HG00733.hp1 HG00738.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.55-3499T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100097008 | ||||||
| chr8:100097013
|
T | C | 3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045 | 3 | HG00735.hp2 HG01081.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.55-3504A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100097013 | ||||||
| chr8:100097148
|
C | T | 22 | a0001c0001t0001g0118a0001c0001t0001g0128a0001c0001t0001g0129others(19): Show | 22 | HG00733.hp1 HG00738.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.55-3639G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100097148 | ||||||
| chr8:100097178
|
C | G | 61 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0090others(58): Show | 62 | HG00558.hp2 HG00673.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.55-3669G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100097178 | ||||||
| chr8:100097246
|
A | G | 89 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0097others(86): Show | 89 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.55-3737T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100097246 | ||||||
| chr8:100097338
|
A | T | 19 | a0001c0001t0001g0118a0001c0001t0001g0128a0001c0001t0001g0129others(16): Show | 19 | HG00733.hp1 HG00738.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.55-3829T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100097338 | ||||||
| chr8:100097345
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.55-3836A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100097345 | ||||||
| chr8:100097367
|
G | T | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.55-3858C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100097367 | ||||||
| chr8:100097526
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.55-4017C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100097526 | ||||||
| chr8:100097554
|
T | A | 1 | a0001c0001t0001g0211 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.55-4045A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100097554 | ||||||
| chr8:100097780
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.55-4271G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100097780 | ||||||
| chr8:100097796
|
T | C | 225 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0008others(222): Show | 227 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.55-4287A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100097796 | ||||||
| chr8:100097849
|
C | T | 61 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0090others(58): Show | 62 | HG00558.hp2 HG00673.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.55-4340G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100097849 | ||||||
| chr8:100097954
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.55-4445G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100097954 | ||||||
| chr8:100098068
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.55-4559G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098068 | ||||||
| chr8:100098162
|
CAT | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0102others(2): Show | 5 | HG02630.hp1 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.55-4655_55-4654del others(2): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098162 | ||||||
| chr8:100098164
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.55-4655A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098164 | ||||||
| chr8:100098211
|
T | C | 61 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0090others(58): Show | 62 | HG00558.hp2 HG00673.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.55-4702A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098211 | ||||||
| chr8:100098243
|
A | G | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG01109.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.55-4734T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098243 | ||||||
| chr8:100098268
|
G | C | 6 | a0001c0003t0001g0001a0001c0003t0001g0052a0001c0003t0001g0055others(3): Show | 7 | HG02109.hp1 HG02257.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.55-4759C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098268 | ||||||
| chr8:100098323
|
C | T | 91 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0097others(88): Show | 91 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.55-4814G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098323 | ||||||
| chr8:100098364
|
G | T | 61 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0090others(58): Show | 62 | HG00558.hp2 HG00673.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.55-4855C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098364 | ||||||
| chr8:100098403
|
C | T | 2 | a0001c0001t0001g0067a0003c0005t0001g0068 | 2 | HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.55-4894G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098403 | ||||||
| chr8:100098491
|
G | A | 223 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0008others(220): Show | 225 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.55-4982C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098491 | ||||||
| chr8:100098641
|
G | T | 22 | a0001c0001t0001g0118a0001c0001t0001g0128a0001c0001t0001g0129others(19): Show | 22 | HG00733.hp1 HG00738.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.55-5132C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098641 | ||||||
| chr8:100098677
|
T | TTCTCTTC | 83 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0090others(80): Show | 84 | HG00558.hp2 HG00673.hp2 HG00733.hp1 others(81): Show |
intron_variant | MODIFIER | c.55-5175_55-5169dup others(7): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098677 | ||||||
| chr8:100098707
|
T | G | 22 | a0001c0001t0001g0118a0001c0001t0001g0128a0001c0001t0001g0129others(19): Show | 22 | HG00733.hp1 HG00738.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.55-5198A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098707 | ||||||
| chr8:100098755
|
C | G | 6 | a0001c0003t0001g0001a0001c0003t0001g0052a0001c0003t0001g0055others(3): Show | 7 | HG02109.hp1 HG02257.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.55-5246G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098755 | ||||||
| chr8:100098803
|
G | T | 52 | a0000c0021t0001g0150a0001c0001t0001g0090a0001c0001t0001g0093others(49): Show | 53 | HG00558.hp2 HG00673.hp2 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.55-5294C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098803 | ||||||
| chr8:100098833
|
T | C | 22 | a0001c0001t0001g0118a0001c0001t0001g0128a0001c0001t0001g0129others(19): Show | 22 | HG00733.hp1 HG00738.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.55-5324A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098833 | ||||||
| chr8:100098837
|
ATT | A | 200 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0008others(197): Show | 202 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.55-5330_55-5329del others(2): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098837 | ||||||
| chr8:100098839
|
TTTTTTA | T | 17 | a0001c0001t0001g0118a0001c0001t0001g0128a0001c0001t0001g0129others(14): Show | 17 | HG00733.hp1 HG00738.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.55-5336_55-5331del others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098839 | ||||||
| chr8:100098843
|
T | A | 5 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(2): Show | 5 | HG01109.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.55-5334A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098843 | ||||||
| chr8:100098844
|
TA | T | 5 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(2): Show | 5 | HG01109.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.55-5336delT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098844 | ||||||
| chr8:100098847
|
TTATTTTA others(17): Show |
T | 8 | a0001c0001t0001g0090a0001c0001t0001g0093a0001c0001t0001g0293others(5): Show | 8 | HG00558.hp2 HG03453.hp1 HG03927.hp2 others(5): Show |
intron_variant | MODIFIER | c.55-5362_55-5339del others(24): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098847 | ||||||
| chr8:100098847
|
TTATTTTA others(22): Show |
T | 38 | a0000c0021t0001g0150a0001c0001t0001g0212a0001c0001t0001g0290others(35): Show | 39 | HG00597.hp1 HG00673.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.55-5367_55-5339del others(29): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098847 | ||||||
| chr8:100098847
|
TTATTTTA others(27): Show |
T | 25 | a0001c0001t0001g0036a0001c0001t0001g0145a0001c0001t0001g0157others(22): Show | 26 | HG00609.hp1 HG00621.hp1 HG02451.hp2 others(23): Show |
intron_variant | MODIFIER | c.55-5372_55-5339del others(34): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098847 | ||||||
| chr8:100098847
|
TTATTTTA others(32): Show |
T | 88 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0047others(85): Show | 88 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.55-5377_55-5339del others(39): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098847 | ||||||
| chr8:100098847
|
TTATTTTA others(37): Show |
T | 13 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0102others(10): Show | 13 | HG00408.hp1 HG00558.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.55-5382_55-5339del others(44): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098847 | ||||||
| chr8:100098847
|
TTATTTTA others(42): Show |
T | 3 | a0001c0001t0001g0159a0001c0009t0001g0100a0001c0009t0001g0101 | 3 | HG02056.hp1 HG02486.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.55-5387_55-5339del others(49): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098847 | ||||||
| chr8:100098847
|
TTATTTTA others(47): Show |
T | 2 | a0001c0003t0001g0140a0001c0003t0001g0214 | 2 | NA18962.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.55-5392_55-5339del others(54): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098847 | ||||||
| chr8:100098847
|
TTATTTTA others(52): Show |
T | 23 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0019others(20): Show | 23 | HG00099.hp1 HG00735.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.55-5397_55-5339del others(59): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098847 | ||||||
| chr8:100098854
|
A | ATT | 4 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 4 | HG01109.hp1 HG03098.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.55-5347_55-5346dup others(2): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098854 | ||||||
| chr8:100098855
|
TTATTTTA | T | 17 | a0001c0001t0001g0118a0001c0001t0001g0128a0001c0001t0001g0129others(14): Show | 17 | HG00733.hp1 HG00738.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.55-5353_55-5347del others(7): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098855 | ||||||
| chr8:100098861
|
T | A | 1 | a0001c0012t0001g0131 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.55-5352A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098861 | ||||||
| chr8:100098862
|
A | AT | 4 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 4 | HG01109.hp1 HG03098.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.55-5354dupA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098862 | ||||||
| chr8:100098862
|
A | ATTTAT | 17 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(14): Show | 17 | HG01952.hp2 HG01993.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.55-5358_55-5354dup others(5): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098862 | ||||||
| chr8:100098862
|
A | ATTTATTT others(3): Show |
1 | a0001c0001t0001g0031 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.55-5363_55-5354dup others(10): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098862 | ||||||
| chr8:100098862
|
A | ATTTATTT others(8): Show |
1 | a0001c0001t0001g0253 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-5368_55-5354dup others(15): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098862 | ||||||
| chr8:100098862
|
A | T | 1 | a0001c0012t0001g0131 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.55-5353T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098862 | ||||||
| chr8:100098862
|
ATTTAT | A | 23 | a0000c0019t0001g0248a0001c0001t0001g0007a0001c0001t0001g0028others(20): Show | 23 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.55-5358_55-5354del others(5): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098862 | ||||||
| chr8:100098862
|
ATTTATTT others(3): Show |
A | 5 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(2): Show | 5 | HG01071.hp1 HG01175.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.55-5363_55-5354del others(10): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098862 | ||||||
| chr8:100098862
|
ATTTATTT others(8): Show |
A | 1 | a0001c0024t0001g0299 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.55-5368_55-5354del others(15): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098862 | ||||||
| chr8:100098866
|
ATTTTATT others(4): Show |
A | 1 | a0001c0012t0001g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.55-5368_55-5358del others(11): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098866 | ||||||
| chr8:100098876
|
AT | A | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG01109.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.55-5368delA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098876 | ||||||
| chr8:100098891
|
AT | A | 17 | a0001c0001t0001g0118a0001c0001t0001g0128a0001c0001t0001g0129others(14): Show | 17 | HG00733.hp1 HG00738.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.55-5383delA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098891 | ||||||
| chr8:100098924
|
TTA | T | 17 | a0001c0001t0001g0118a0001c0001t0001g0128a0001c0001t0001g0129others(14): Show | 17 | HG00733.hp1 HG00738.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.55-5417_55-5416del others(2): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098924 | ||||||
| chr8:100098927
|
T | A | 17 | a0001c0001t0001g0118a0001c0001t0001g0128a0001c0001t0001g0129others(14): Show | 17 | HG00733.hp1 HG00738.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.55-5418A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098927 | ||||||
| chr8:100098927
|
T | TTTA | 5 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(2): Show | 5 | HG01109.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.55-5421_55-5419dup others(3): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098927 | ||||||
| chr8:100098965
|
G | C | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.55-5456C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100098965 | ||||||
| chr8:100099019
|
G | A | 2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.55-5510C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100099019 | ||||||
| chr8:100099165
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.55-5656G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100099165 | ||||||
| chr8:100099203
|
T | C | 61 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0090others(58): Show | 62 | HG00558.hp2 HG00673.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.55-5694A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100099203 | ||||||
| chr8:100099310
|
C | G | 16 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(13): Show | 16 | HG02145.hp1 HG02280.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.55-5801G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100099310 | ||||||
| chr8:100099402
|
A | T | 1 | a0001c0001t0001g0157 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.55-5893T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100099402 | ||||||
| chr8:100099409
|
A | G | 61 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0090others(58): Show | 62 | HG00558.hp2 HG00673.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.55-5900T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100099409 | ||||||
| chr8:100099648
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.54+5726A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100099648 | ||||||
| chr8:100099742
|
A | G | 1 | a0001c0003t0001g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.54+5632T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100099742 | ||||||
| chr8:100099852
|
C | T | 3 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0252 | 3 | HG00609.hp2 HG02027.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.54+5522G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100099852 | ||||||
| chr8:100099983
|
A | G | 2 | a0003c0005t0001g0094a0003c0005t0001g0095 | 2 | NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.54+5391T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100099983 | ||||||
| chr8:100100112
|
C | T | 61 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0090others(58): Show | 62 | HG00558.hp2 HG00673.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.54+5262G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100100112 | ||||||
| chr8:100100267
|
T | A | 60 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0090others(57): Show | 61 | HG00558.hp2 HG00673.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.54+5107A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100100267 | ||||||
| chr8:100100276
|
T | C | 60 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0090others(57): Show | 61 | HG00558.hp2 HG00673.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.54+5098A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100100276 | ||||||
| chr8:100100291
|
A | AT | 14 | a0000c0019t0001g0248a0001c0001t0001g0004a0001c0001t0001g0099others(11): Show | 14 | HG00673.hp1 HG01109.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.54+5082dupA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100100291 | ||||||
| chr8:100100291
|
A | ATTT | 47 | a0000c0021t0001g0150a0001c0001t0001g0090a0001c0001t0001g0145others(44): Show | 48 | HG00558.hp2 HG00673.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.54+5080_54+5082dup others(3): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100100291 | ||||||
| chr8:100100355
|
T | C | 139 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0019others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.54+5019A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100100355 | ||||||
| chr8:100100409
|
C | T | 7 | a0003c0005t0001g0002a0003c0005t0001g0106a0003c0005t0001g0107others(4): Show | 8 | HG02451.hp2 HG02486.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.54+4965G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100100409 | ||||||
| chr8:100100448
|
T | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | NA18954.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.54+4926A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100100448 | ||||||
| chr8:100100478
|
C | T | 4 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(1): Show | 4 | HG01496.hp2 HG02004.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.54+4896G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100100478 | ||||||
| chr8:100100526
|
G | A | 89 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0097others(86): Show | 89 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.54+4848C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100100526 | ||||||
| chr8:100100575
|
C | G | 20 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0048others(17): Show | 20 | HG02145.hp1 HG02280.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.54+4799G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100100575 | ||||||
| chr8:100100588
|
C | G | 60 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0090others(57): Show | 61 | HG00558.hp2 HG00673.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.54+4786G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100100588 | ||||||
| chr8:100100928
|
G | A | 2 | a0003c0005t0001g0094a0003c0005t0001g0095 | 2 | NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.54+4446C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100100928 | ||||||
| chr8:100101068
|
G | A | 3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244 | 3 | HG01496.hp2 HG02004.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.54+4306C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100101068 | ||||||
| chr8:100101143
|
A | C | 4 | a0001c0003t0001g0074a0001c0003t0001g0075a0001c0003t0001g0076others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.54+4231T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100101143 | ||||||
| chr8:100101290
|
CT | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0032a0001c0001t0001g0099others(5): Show | 8 | HG02486.hp2 HG02572.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.54+4083delA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100101290 | ||||||
| chr8:100101318
|
G | A | 2 | a0001c0009t0001g0100a0001c0009t0001g0101 | 2 | HG02486.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.54+4056C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100101318 | ||||||
| chr8:100101411
|
C | T | 179 | a0000c0021t0001g0150a0001c0001t0001g0006a0001c0001t0001g0007others(176): Show | 181 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.54+3963G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100101411 | ||||||
| chr8:100101443
|
A | AT | 6 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0247others(3): Show | 6 | HG01255.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.54+3930dupA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100101443 | ||||||
| chr8:100101443
|
AT | A | 49 | a0001c0001t0001g0004a0001c0001t0001g0090a0001c0001t0001g0093others(46): Show | 50 | HG00738.hp1 HG01081.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.54+3930delA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100101443 | ||||||
| chr8:100101443
|
ATT | A | 120 | a0000c0021t0001g0150a0001c0001t0001g0034a0001c0001t0001g0036others(117): Show | 120 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.54+3929_54+3930del others(2): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100101443 | ||||||
| chr8:100101443
|
ATTT | A | 76 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(73): Show | 77 | HG00099.hp1 HG00438.hp2 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.54+3928_54+3930del others(3): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100101443 | ||||||
| chr8:100101515
|
G | C | 3 | a0001c0003t0001g0064a0001c0004t0002g0062a0001c0004t0002g0063 | 3 | HG02647.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.54+3859C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100101515 | ||||||
| chr8:100101584
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.54+3790G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100101584 | ||||||
| chr8:100101759
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.54+3615A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100101759 | ||||||
| chr8:100102005
|
T | C | 1 | a0001c0001t0001g0286 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.54+3369A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100102005 | ||||||
| chr8:100102088
|
C | A | 1 | a0001c0001t0001g0295 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.54+3286G>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100102088 | ||||||
| chr8:100102272
|
T | C | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.54+3102A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100102272 | ||||||
| chr8:100102322
|
C | T | 2 | a0001c0004t0002g0115a0001c0004t0002g0116 | 2 | HG00733.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.54+3052G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100102322 | ||||||
| chr8:100102353
|
A | G | 62 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(59): Show | 62 | HG00099.hp1 HG00438.hp2 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.54+3021T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100102353 | ||||||
| chr8:100102476
|
CAG | C | 3 | a0001c0001t0001g0050a0001c0001t0001g0051a0002c0002t0001g0033 | 3 | HG01071.hp2 HG01074.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.54+2896_54+2897del others(2): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100102476 | ||||||
| chr8:100102551
|
G | C | 1 | a0001c0003t0001g0064 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.54+2823C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100102551 | ||||||
| chr8:100102566
|
C | T | 101 | a0000c0021t0001g0150a0001c0001t0001g0034a0001c0001t0001g0137others(98): Show | 101 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.54+2808G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100102566 | ||||||
| chr8:100102730
|
A | T | 1 | a0001c0003t0001g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.54+2644T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100102730 | ||||||
| chr8:100102923
|
T | C | 1 | a0011c0016t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.54+2451A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100102923 | ||||||
| chr8:100103131
|
G | T | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.54+2243C>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100103131 | ||||||
| chr8:100103640
|
G | GA | 101 | a0000c0021t0001g0150a0001c0001t0001g0034a0001c0001t0001g0137others(98): Show | 101 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.54+1733dupT | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100103640 | ||||||
| chr8:100103661
|
CAGG | C | 32 | a0001c0001t0001g0090a0001c0001t0001g0093a0001c0001t0001g0097others(29): Show | 33 | HG01081.hp1 HG02109.hp1 HG02257.hp1 others(30): Show |
intron_variant | MODIFIER | c.54+1710_54+1712del others(3): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100103661 | ||||||
| chr8:100103834
|
G | A | 25 | a0001c0001t0001g0118a0001c0001t0001g0128a0001c0001t0001g0129others(22): Show | 25 | HG00733.hp1 HG00738.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.54+1540C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100103834 | ||||||
| chr8:100103975
|
G | A | 22 | a0001c0001t0001g0118a0001c0001t0001g0128a0001c0001t0001g0129others(19): Show | 22 | HG00733.hp1 HG00738.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.54+1399C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100103975 | ||||||
| chr8:100104201
|
A | C | 204 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0006others(201): Show | 205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.54+1173T>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100104201 | ||||||
| chr8:100104329
|
C | CGT | 80 | a0000c0019t0001g0248a0001c0001t0001g0004a0001c0001t0001g0035others(77): Show | 81 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.54+1043_54+1044dup others(2): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100104329 | ||||||
| chr8:100104329
|
C | CGTGT | 16 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(13): Show | 16 | HG00544.hp1 HG01123.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.54+1041_54+1044dup others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100104329 | ||||||
| chr8:100104329
|
C | CGTGTGT | 14 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(11): Show | 14 | HG02300.hp1 HG02486.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.54+1039_54+1044dup others(6): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100104329 | ||||||
| chr8:100104329
|
C | CGTGTGTG others(1): Show |
15 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(12): Show | 15 | HG01257.hp1 HG01258.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.54+1037_54+1044dup others(8): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100104329 | ||||||
| chr8:100104329
|
C | CGTGTGTG others(3): Show |
2 | a0001c0001t0001g0008a0001c0003t0001g0009 | 2 | HG03654.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.54+1035_54+1044dup others(10): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100104329 | ||||||
| chr8:100104329
|
C | CGTGTGTG others(5): Show |
1 | a0001c0001t0001g0007 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.54+1033_54+1044dup others(12): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100104329 | ||||||
| chr8:100104329
|
CGT | C | 10 | a0001c0001t0001g0098a0001c0001t0001g0138a0001c0001t0001g0139others(7): Show | 10 | HG00438.hp1 HG00738.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.54+1043_54+1044del others(2): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100104329 | ||||||
| chr8:100104329
|
CGTGT | C | 97 | a0000c0021t0001g0150a0001c0001t0001g0141a0001c0001t0001g0143others(94): Show | 97 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.54+1041_54+1044del others(4): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100104329 | ||||||
| chr8:100104361
|
T | TGTA | 19 | a0001c0001t0001g0118a0001c0001t0001g0128a0001c0001t0001g0129others(16): Show | 19 | HG00733.hp1 HG00738.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.54+1012_54+1013ins others(3): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100104361 | ||||||
| chr8:100104361
|
T | TGTGTA | 3 | a0001c0004t0002g0114a0001c0012t0001g0112a0006c0007t0001g0113 | 3 | HG01884.hp1 HG01884.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.54+1012_54+1013ins others(5): Show |
RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100104361 | ||||||
| chr8:100104362
|
A | G | 1 | a0001c0001t0001g0231 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.54+1012T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100104362 | ||||||
| chr8:100104362
|
A | T | 22 | a0001c0001t0001g0118a0001c0001t0001g0128a0001c0001t0001g0129others(19): Show | 22 | HG00733.hp1 HG00738.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.54+1012T>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100104362 | ||||||
| chr8:100104362
|
AT | A | 8 | a0001c0001t0001g0111a0003c0005t0001g0002a0003c0005t0001g0106others(5): Show | 9 | HG02451.hp2 HG02486.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.54+1011delA | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100104362 | ||||||
| chr8:100104447
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.54+927G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100104447 | ||||||
| chr8:100104518
|
G | A | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG02683.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.54+856C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100104518 | ||||||
| chr8:100104536
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.54+838A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100104536 | ||||||
| chr8:100104558
|
G | C | 142 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0099others(139): Show | 143 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.54+816C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100104558 | ||||||
| chr8:100104582
|
T | A | 25 | a0001c0001t0001g0118a0001c0001t0001g0128a0001c0001t0001g0129others(22): Show | 25 | HG00733.hp1 HG00738.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.54+792A>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100104582 | ||||||
| chr8:100104776
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.54+598C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100104776 | ||||||
| chr8:100104791
|
T | C | 1 | a0001c0001t0001g0297 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.54+583A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100104791 | ||||||
| chr8:100104796
|
G | C | 28 | a0001c0001t0001g0004a0001c0001t0001g0118a0001c0001t0001g0128others(25): Show | 28 | HG00733.hp1 HG00738.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.54+578C>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100104796 | ||||||
| chr8:100104971
|
C | G | 1 | a0001c0001t0001g0006 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.54+403G>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100104971 | ||||||
| chr8:100104985
|
T | C | 2 | a0001c0001t0001g0298a0002c0002t0001g0133 | 2 | HG02818.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.54+389A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100104985 | ||||||
| chr8:100104992
|
T | C | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG01109.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.54+382A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100104992 | ||||||
| chr8:100105313
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0003g0003a0001c0003t0001g0005 | 3 | HG01243.hp2 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.54+61G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100105313 | ||||||
| chr8:100105326
|
T | G | 100 | a0000c0021t0001g0150a0001c0001t0001g0137a0001c0001t0001g0138others(97): Show | 100 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.54+48A>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 2/27 | chr8 | 100105326 | ||||||
| chr8:100105434
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0003g0003a0001c0003t0001g0005 | 3 | HG01243.hp2 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.26-32G>A | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 1/27 | chr8 | 100105434 | ||||||
| chr8:100105506
|
A | G | 238 | a0000c0021t0001g0150a0001c0001t0001g0004a0001c0001t0001g0006others(235): Show | 240 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.26-104T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 1/27 | chr8 | 100105506 | ||||||
| chr8:100105759
|
G | A | 6 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0302others(3): Show | 6 | NA18960.hp1 NA18977.hp1 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+138C>T | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 1/27 | chr8 | 100105759 | ||||||
| chr8:100105785
|
T | C | 1 | a0002c0002t0001g0306 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.25+112A>G | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 1/27 | chr8 | 100105785 | ||||||
| chr8:100105806
|
A | G | 3 | a0001c0001t0001g0004a0001c0001t0003g0003a0001c0003t0001g0005 | 3 | HG01243.hp2 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.25+91T>C | RGS22 | ENSG00000132554.21 | transcript | ENST00000360863.11 | protein_coding | 1/27 | chr8 | 100105806 |