Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 401190 |
|---|---|
| ensemblid | ENSG00000186479.5 |
| hgncid | 23271 |
| symbol | RGS7BP |
| name | regulator of G protein signaling 7 binding protein |
| refseq_nuc | NM_001029875.3 |
| refseq_prot | NP_001025046.1 |
| ensembl_nuc | ENST00000334025.3 |
| ensembl_prot | ENSP00000334851.2 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 64506015 |
| end | 64612319 |
| strand | + |
| ver | v1.2 |
| region | chr5:64506015-64612319 |
| region5000 | chr5:64501015-64617319 |
| regionname0 | RGS7BP_chr5_64506015_64612319 |
| regionname5000 | RGS7BP_chr5_64501015_64617319 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 257 | 195 | 65 | 46 | 52 | 6 | 25 | 39 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| a0002 | 1/0 | 257 | 83 | 19 | 13 | 37 | 0 | 13 | 30 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| a0003 | 0/0 | 257 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| a0004 | 0/0 | 257 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| 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 | 0/1 | 774 | 195 | 65 | 46 | 52 | 6 | 25 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| c0002 | 1/0 | 774 | 83 | 19 | 13 | 37 | 0 | 13 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| c0003 | 0/0 | 774 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| c0004 | 0/0 | 774 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 3678 | 105 | 53 | 25 | 9 | 3 | 15 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| t0002 | 0/0 | 3677 | 61 | 11 | 14 | 26 | 2 | 8 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| t0003 | 1/0 | 3678 | 46 | 0 | 3 | 34 | 0 | 8 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| t0004 | 0/0 | 3678 | 35 | 7 | 11 | 16 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| t0005 | 0/0 | 3677 | 5 | 0 | 0 | 5 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| t0006 | 0/0 | 3678 | 4 | 4 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| t0007 | 0/0 | 3677 | 4 | 0 | 0 | 0 | 0 | 4 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| t0008 | 0/0 | 3678 | 2 | 1 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| t0009 | 0/0 | 3678 | 2 | 2 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| t0010 | 0/0 | 3677 | 2 | 0 | 2 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| t0011 | 0/0 | 3678 | 2 | 2 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| t0012 | 0/0 | 3678 | 2 | 0 | 2 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| t0013 | 0/0 | 3678 | 2 | 2 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| t0014 | 0/0 | 3677 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| t0015 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| t0016 | 0/0 | 3677 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| t0017 | 0/0 | 3678 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| t0018 | 0/0 | 3677 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| t0019 | 0/1 | 3678 | 1 | 0 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| t0020 | 0/0 | 3678 | 1 | 0 | 0 | 0 | 1 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| t0021 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0004 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0064 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0226 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 774 | 195 | 65 | 46 | 52 | 6 | 25 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| a0002c0002 | 1/0 | 774 | 83 | 19 | 13 | 37 | 0 | 13 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| a0003c0004 | 0/0 | 774 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| a0004c0003 | 0/0 | 774 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4451 | 70 | 35 | 16 | 6 | 3 | 10 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| a0001c0001t0002 | 0/0 | 4450 | 59 | 11 | 13 | 25 | 2 | 8 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| a0001c0001t0004 | 0/0 | 4451 | 35 | 7 | 11 | 16 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| a0001c0001t0005 | 0/0 | 4450 | 5 | 0 | 0 | 5 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| a0001c0001t0006 | 0/0 | 4451 | 3 | 3 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| a0001c0001t0007 | 0/0 | 4450 | 4 | 0 | 0 | 0 | 0 | 4 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| a0001c0001t0008 | 0/0 | 4451 | 2 | 1 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| a0001c0001t0009 | 0/0 | 4451 | 2 | 2 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| a0001c0001t0010 | 0/0 | 4450 | 2 | 0 | 2 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| a0001c0001t0011 | 0/0 | 4451 | 2 | 2 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| a0001c0001t0012 | 0/0 | 4451 | 2 | 0 | 2 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| a0001c0001t0013 | 0/0 | 4451 | 2 | 2 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| a0001c0001t0014 | 0/0 | 4450 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| a0001c0001t0015 | 0/0 | 4451 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| a0001c0001t0016 | 0/0 | 4450 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| a0001c0001t0018 | 0/0 | 4450 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| a0001c0001t0019 | 0/1 | 4451 | 1 | 0 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| a0001c0001t0020 | 0/0 | 4451 | 1 | 0 | 0 | 0 | 1 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| a0001c0001t0021 | 0/0 | 4451 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| a0002c0002t0001 | 0/0 | 4451 | 35 | 18 | 9 | 3 | 0 | 5 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| a0002c0002t0003 | 1/0 | 4451 | 46 | 0 | 3 | 34 | 0 | 8 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| a0002c0002t0006 | 0/0 | 4451 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| a0002c0002t0017 | 0/0 | 4451 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| a0003c0004t0002 | 0/0 | 4450 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| a0004c0003t0002 | 0/0 | 4450 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | copy fasta | chr5 | 64501015 | 64617319 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0005g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0005g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0005g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0006g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0006g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0006g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0007g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0007g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0007g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0008g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0008g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0009g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0009g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0010g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0010g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0011g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0011g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0012g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0012g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0013g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0013g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0014g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0015g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0016g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0018g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0019g0226 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0020g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0001c0001t0021g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0004 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0064 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0006g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0002c0002t0017g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0003c0004t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| a0004c0003t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | GBR | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0125 | EUR | GBR | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG00423 | hp1 | a0002 | c0002 | t0003 | g0140 | EAS | CHS | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG00423 | hp2 | a0002 | c0002 | t0003 | g0050 | EAS | CHS | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG00558 | hp1 | a0002 | c0002 | t0003 | g0207 | EAS | CHS | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0143 | EAS | CHS | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG00597 | hp1 | a0002 | c0002 | t0003 | g0105 | EAS | CHS | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | CHS | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG00621 | hp1 | a0002 | c0002 | t0003 | g0129 | EAS | CHS | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0203 | EAS | CHS | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | PUR | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0083 | AMR | PUR | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG00642 | hp2 | a0001 | c0001 | t0010 | g0019 | AMR | PUR | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG00738 | hp2 | a0002 | c0002 | t0003 | g0162 | AMR | PUR | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01074 | hp1 | a0002 | c0002 | t0003 | g0042 | AMR | PUR | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0268 | AMR | PUR | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0270 | AMR | PUR | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0084 | AMR | PUR | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01106 | hp2 | a0002 | c0002 | t0017 | g0227 | AMR | PUR | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01109 | hp1 | a0001 | c0001 | t0008 | g0257 | AMR | PUR | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0186 | AMR | PUR | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01167 | hp2 | a0001 | c0001 | t0010 | g0233 | AMR | PUR | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0260 | AMR | PUR | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0235 | AMR | CLM | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0223 | AMR | CLM | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01257 | hp2 | a0001 | c0001 | t0012 | g0127 | AMR | CLM | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01258 | hp1 | a0001 | c0001 | t0012 | g0146 | AMR | CLM | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0236 | AMR | CLM | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | CLM | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | CLM | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0266 | AMR | CLM | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | CLM | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0234 | AMR | CLM | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0080 | EUR | IBS | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01515 | hp2 | a0001 | c0001 | t0020 | g0101 | EUR | IBS | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0020 | EUR | IBS | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0121 | EUR | IBS | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01884 | hp1 | a0001 | c0001 | t0015 | g0017 | AFR | ACB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0182 | AFR | ACB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0007 | AFR | ACB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0200 | AMR | PEL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0265 | AMR | PEL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | PEL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PEL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | PEL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0238 | AMR | PEL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0263 | AMR | PEL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0271 | AMR | PEL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0262 | AMR | PEL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01993 | hp2 | a0001 | c0001 | t0016 | g0261 | AMR | PEL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0204 | AMR | PEL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0158 | EAS | KHV | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | KHV | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0054 | AFR | ACB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0274 | EAS | KHV | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02056 | hp2 | a0002 | c0002 | t0003 | g0155 | EAS | KHV | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | KHV | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | KHV | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | KHV | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0087 | AFR | ACB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0229 | AFR | ACB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | ACB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0179 | AFR | ACB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0208 | AMR | PEL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0256 | AMR | PEL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0185 | AFR | ACB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0091 | AFR | ACB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0202 | AMR | PEL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02293 | hp2 | a0003 | c0004 | t0002 | g0215 | AMR | PEL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0220 | AMR | PEL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02451 | hp1 | a0001 | c0001 | t0011 | g0013 | AFR | ACB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | ACB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0037 | AFR | GWD | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0196 | SAS | PJL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0027 | AFR | GWD | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0090 | AFR | GWD | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02647 | hp1 | a0001 | c0001 | t0013 | g0008 | AFR | GWD | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0273 | AFR | GWD | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0086 | AFR | GWD | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0195 | SAS | PJL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0180 | AFR | GWD | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0181 | AFR | GWD | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0036 | AFR | GWD | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02922 | hp1 | a0001 | c0001 | t0009 | g0176 | AFR | ESN | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | ESN | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0183 | AFR | ESN | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0225 | SAS | PJL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | GWD | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0028 | AFR | GWD | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03098 | hp1 | a0001 | c0001 | t0021 | g0010 | AFR | MSL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0240 | AFR | ESN | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | ESN | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ESN | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | MSL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0038 | SAS | PJL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03239 | hp2 | a0002 | c0002 | t0003 | g0131 | SAS | PJL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | MSL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03453 | hp2 | a0001 | c0001 | t0011 | g0014 | AFR | MSL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0041 | AFR | MSL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03486 | hp2 | a0002 | c0002 | t0006 | g0085 | AFR | MSL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03490 | hp1 | a0002 | c0002 | t0003 | g0032 | SAS | PJL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0232 | SAS | PJL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0239 | SAS | PJL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03491 | hp2 | a0001 | c0001 | t0007 | g0003 | SAS | PJL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03492 | hp1 | a0001 | c0001 | t0007 | g0003 | SAS | PJL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03492 | hp2 | a0002 | c0002 | t0003 | g0033 | SAS | PJL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03669 | hp1 | a0002 | c0002 | t0003 | g0110 | SAS | PJL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03669 | hp2 | a0001 | c0001 | t0014 | g0025 | SAS | PJL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0198 | SAS | PJL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03704 | hp2 | a0002 | c0002 | t0003 | g0112 | SAS | PJL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0217 | SAS | PJL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0221 | SAS | PJL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0243 | SAS | BEB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03831 | hp2 | a0002 | c0002 | t0003 | g0062 | SAS | BEB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | BEB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03834 | hp2 | a0001 | c0001 | t0018 | g0210 | SAS | BEB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03927 | hp1 | a0001 | c0001 | t0007 | g0039 | SAS | BEB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03942 | hp1 | a0002 | c0002 | t0003 | g0249 | SAS | BEB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03942 | hp2 | a0001 | c0001 | t0007 | g0056 | SAS | BEB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0228 | SAS | STU | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | STU | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0216 | SAS | STU | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG04204 | hp2 | a0002 | c0002 | t0003 | g0199 | SAS | STU | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | STU | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0264 | SAS | STU | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0157 | AFR | YRI | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | YRI | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0065 | EAS | CHB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18612 | hp2 | a0002 | c0002 | t0003 | g0134 | EAS | CHB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | CHB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0099 | EAS | CHB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0092 | AFR | YRI | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0255 | AFR | YRI | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18939 | hp1 | a0002 | c0002 | t0003 | g0171 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18941 | hp2 | a0002 | c0002 | t0003 | g0031 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18942 | hp1 | a0002 | c0002 | t0003 | g0154 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18945 | hp1 | a0002 | c0002 | t0003 | g0252 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18946 | hp1 | a0002 | c0002 | t0003 | g0163 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18946 | hp2 | a0002 | c0002 | t0003 | g0128 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0197 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18951 | hp1 | a0001 | c0001 | t0005 | g0190 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18957 | hp1 | a0002 | c0002 | t0003 | g0201 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0139 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18965 | hp2 | a0002 | c0002 | t0003 | g0079 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18967 | hp1 | a0001 | c0001 | t0004 | g0135 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18977 | hp1 | a0002 | c0002 | t0003 | g0130 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18978 | hp1 | a0002 | c0002 | t0003 | g0133 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18979 | hp1 | a0002 | c0002 | t0003 | g0119 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0167 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18981 | hp2 | a0001 | c0001 | t0005 | g0136 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18983 | hp1 | a0002 | c0002 | t0003 | g0193 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18986 | hp1 | a0002 | c0002 | t0003 | g0191 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18986 | hp2 | a0001 | c0001 | t0005 | g0123 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18998 | hp1 | a0002 | c0002 | t0003 | g0073 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19007 | hp1 | a0002 | c0002 | t0003 | g0156 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19007 | hp2 | a0002 | c0002 | t0003 | g0049 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0142 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19009 | hp2 | a0002 | c0002 | t0003 | g0107 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19010 | hp1 | a0002 | c0002 | t0003 | g0098 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19011 | hp2 | a0002 | c0002 | t0003 | g0051 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | LWK | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | LWK | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | LWK | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19043 | hp2 | a0001 | c0001 | t0013 | g0009 | AFR | LWK | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19054 | hp1 | a0002 | c0002 | t0003 | g0161 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19058 | hp1 | a0002 | c0002 | t0003 | g0224 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19058 | hp2 | a0001 | c0001 | t0005 | g0272 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19064 | hp1 | a0004 | c0003 | t0002 | g0244 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19064 | hp2 | a0002 | c0002 | t0003 | g0164 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0245 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19068 | hp2 | a0002 | c0002 | t0003 | g0147 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19070 | hp1 | a0002 | c0002 | t0003 | g0117 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19084 | hp1 | a0002 | c0002 | t0003 | g0170 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19087 | hp1 | a0001 | c0001 | t0005 | g0116 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19088 | hp2 | a0002 | c0002 | t0003 | g0071 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19091 | hp1 | a0002 | c0002 | t0003 | g0206 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0048 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0088 | AFR | YRI | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | YRI | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0187 | AFR | ASW | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0267 | AFR | ASW | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0222 | AMR | CLM | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG01123 | hp2 | a0002 | c0002 | t0003 | g0081 | AMR | CLM | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | ACB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0184 | AFR | ACB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0254 | AFR | ACB | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | USA | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | USA | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | LWK | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0172 | AFR | LWK | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0019 | g0226 | REF | REF | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0003 | g0064 | REF | REF | RGS7BP_chr5_64501015_64617319 | RGS7BP | chr5 | 64501015 | 64617319 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:64506738
|
C | G | 1 | a0003 | 1 | HG02293.hp2 | missense_variant | MODERATE | c.114C>G | p.Ser38Arg | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 1/6 | 724/4451 | 114/774 | 38/257 | chr5 | 64506738 | ||
| chr5:64594741
|
G | C | 1 | a0004 | 1 | NA19064.hp1 | missense_variant | MODERATE | c.495G>C | p.Leu165Phe | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 4/6 | 1105/4451 | 495/774 | 165/257 | chr5 | 64594741 | ||
| chr5:64609241
|
A | G | 3 | a0001a0003a0004 | 197 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(194): Show |
missense_variant | MODERATE | c.763A>G | p.Ile255Val | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 6/6 | 1373/4451 | 763/774 | 255/257 | chr5 | 64609241 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:64506252
|
C | T | 2 | a0001c0001t0013a0001c0001t0021 | 3 | HG02647.hp1 HG03098.hp1 NA19043.hp2 |
5_prime_UTR_variant | MODIFIER | c.-373C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 1/6 | 373 | chr5 | 64506252 | |||||
| chr5:64506352
|
G | C | 1 | a0001c0001t0014 | 1 | HG03669.hp2 | 5_prime_UTR_variant | MODIFIER | c.-273G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 1/6 | 273 | chr5 | 64506352 | |||||
| chr5:64506567
|
G | C | 3 | a0001c0001t0006a0001c0001t0015a0002c0002t0006 | 5 | HG01884.hp1 HG02257.hp1 HG02717.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-58G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 1/6 | 58 | chr5 | 64506567 | |||||
| chr5:64609318
|
A | T | 1 | a0001c0001t0020 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*66A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 6/6 | 66 | chr5 | 64609318 | |||||
| chr5:64609523
|
T | A | 1 | a0001c0001t0004 | 35 | HG00558.hp2 HG00621.hp2 HG00639.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*271T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 6/6 | 271 | chr5 | 64609523 | |||||
| chr5:64610475
|
C | T | 1 | a0001c0001t0012 | 2 | HG01257.hp2 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1223C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 6/6 | 1223 | chr5 | 64610475 | |||||
| chr5:64610477
|
C | G | 2 | a0001c0001t0011a0001c0001t0015 | 3 | HG01884.hp1 HG02451.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1225C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 6/6 | 1225 | chr5 | 64610477 | |||||
| chr5:64610589
|
C | T | 1 | a0001c0001t0019 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1337C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 6/6 | 1337 | chr5 | 64610589 | |||||
| chr5:64610758
|
G | T | 24 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(21): Show | 234 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(231): Show |
3_prime_UTR_variant | MODIFIER | c.*1506G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 6/6 | 1506 | chr5 | 64610758 | |||||
| chr5:64610769
|
G | A | 2 | a0001c0001t0008a0001c0001t0021 | 3 | HG01109.hp1 HG01891.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1517G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 6/6 | 1517 | chr5 | 64610769 | |||||
| chr5:64611021
|
G | A | 1 | a0001c0001t0016 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1769G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 6/6 | 1769 | chr5 | 64611021 | |||||
| chr5:64611074
|
A | C | 10 | a0001c0001t0002a0001c0001t0007a0001c0001t0010others(7): Show | 73 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*1822A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 6/6 | 1822 | chr5 | 64611074 | |||||
| chr5:64611437
|
A | G | 2 | a0001c0001t0008a0001c0001t0021 | 3 | HG01109.hp1 HG01891.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2185A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 6/6 | 2185 | chr5 | 64611437 | |||||
| chr5:64611443
|
G | A | 1 | a0001c0001t0007 | 4 | HG03491.hp2 HG03492.hp1 HG03927.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2191G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 6/6 | 2191 | chr5 | 64611443 | |||||
| chr5:64611836
|
CA | C | 1 | a0001c0001t0005 | 5 | NA18951.hp1 NA18981.hp2 NA18986.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2585delA | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 6/6 | 2585 | chr5 | 64611836 | |||||
| chr5:64611921
|
C | T | 1 | a0001c0001t0009 | 2 | HG02055.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2669C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 6/6 | 2669 | chr5 | 64611921 | |||||
| chr5:64611931
|
T | C | 1 | a0001c0001t0018 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2679T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 6/6 | 2679 | chr5 | 64611931 | |||||
| chr5:64611984
|
T | C | 1 | a0002c0002t0017 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2732T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 6/6 | 2732 | chr5 | 64611984 | |||||
| chr5:64611991
|
G | C | 1 | a0001c0001t0010 | 2 | HG00642.hp2 HG01167.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2739G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 6/6 | 2739 | chr5 | 64611991 | |||||
| chr5:64612124
|
G | A | 2 | a0001c0001t0008a0001c0001t0021 | 3 | HG01109.hp1 HG01891.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2872G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 6/6 | 2872 | chr5 | 64612124 | |||||
| chr5:64612172
|
TC | T | 8 | a0001c0001t0002a0001c0001t0007a0001c0001t0010others(5): Show | 70 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*2922delC | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 6/6 | 2922 | INFO_REALIGN_3_PRIME | chr5 | 64612172 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:64506809
|
C | CT | 85 | a0001c0001t0001g0194a0001c0001t0001g0214a0001c0001t0001g0237others(82): Show | 87 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.165+35dupT | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 64506809 | |||||
| chr5:64506888
|
C | T | 2 | a0001c0001t0005g0190a0002c0002t0003g0191 | 2 | NA18951.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.165+99C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 1/5 | chr5 | 64506888 | ||||||
| chr5:64506969
|
T | G | 1 | a0001c0001t0002g0192 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.165+180T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 1/5 | chr5 | 64506969 | ||||||
| chr5:64507191
|
A | C | 1 | a0001c0001t0004g0274 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.165+402A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 1/5 | chr5 | 64507191 | ||||||
| chr5:64507266
|
G | T | 99 | a0001c0001t0001g0097a0001c0001t0001g0100a0001c0001t0001g0106others(96): Show | 99 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.166-445G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 1/5 | chr5 | 64507266 | ||||||
| chr5:64507315
|
C | T | 19 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0269others(16): Show | 20 | HG01074.hp2 HG01081.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.166-396C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 1/5 | chr5 | 64507315 | ||||||
| chr5:64507515
|
G | A | 69 | a0001c0001t0001g0194a0001c0001t0001g0214a0001c0001t0001g0237others(66): Show | 70 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.166-196G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 1/5 | chr5 | 64507515 | ||||||
| chr5:64508193
|
G | A | 1 | a0002c0002t0001g0095 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.332+316G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64508193 | ||||||
| chr5:64508238
|
C | A | 4 | a0001c0001t0001g0011a0001c0001t0011g0013a0001c0001t0011g0014others(1): Show | 4 | HG02451.hp1 HG03041.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.332+361C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64508238 | ||||||
| chr5:64508456
|
C | A | 1 | a0001c0001t0004g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.332+579C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64508456 | ||||||
| chr5:64508580
|
T | C | 100 | a0001c0001t0001g0097a0001c0001t0001g0100a0001c0001t0001g0106others(97): Show | 100 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.332+703T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64508580 | ||||||
| chr5:64508800
|
T | C | 1 | a0001c0001t0015g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.332+923T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64508800 | ||||||
| chr5:64508872
|
T | C | 4 | a0001c0001t0001g0011a0001c0001t0011g0013a0001c0001t0011g0014others(1): Show | 4 | HG02451.hp1 HG03041.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.332+995T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64508872 | ||||||
| chr5:64509041
|
T | C | 2 | a0001c0001t0002g0002a0001c0001t0002g0018 | 3 | HG03098.hp2 HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.332+1164T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64509041 | ||||||
| chr5:64509416
|
T | C | 1 | a0002c0002t0003g0193 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.332+1539T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64509416 | ||||||
| chr5:64509445
|
C | T | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.332+1568C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64509445 | ||||||
| chr5:64509456
|
A | G | 100 | a0001c0001t0001g0097a0001c0001t0001g0100a0001c0001t0001g0106others(97): Show | 100 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.332+1579A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64509456 | ||||||
| chr5:64509476
|
T | G | 16 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(13): Show | 16 | HG00642.hp2 HG01175.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.332+1599T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64509476 | ||||||
| chr5:64509632
|
C | T | 1 | a0001c0001t0006g0187 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.332+1755C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64509632 | ||||||
| chr5:64509901
|
A | G | 3 | a0001c0001t0013g0008a0001c0001t0013g0009a0001c0001t0021g0010 | 3 | HG02647.hp1 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.332+2024A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64509901 | ||||||
| chr5:64509904
|
C | T | 17 | a0001c0001t0001g0174a0001c0001t0001g0177a0001c0001t0001g0178others(14): Show | 17 | HG01167.hp1 HG01884.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.332+2027C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64509904 | ||||||
| chr5:64509920
|
A | G | 9 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0002g0002others(6): Show | 10 | HG02258.hp1 HG02280.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.332+2043A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64509920 | ||||||
| chr5:64509926
|
A | G | 15 | a0001c0001t0002g0241a0001c0001t0002g0242a0001c0001t0002g0243others(12): Show | 15 | HG02056.hp1 HG02071.hp1 HG03831.hp1 others(12): Show |
intron_variant | MODIFIER | c.332+2049A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64509926 | ||||||
| chr5:64509964
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.332+2087G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64509964 | ||||||
| chr5:64510124
|
C | T | 4 | a0001c0001t0006g0086a0001c0001t0006g0087a0001c0001t0015g0017others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.332+2247C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64510124 | ||||||
| chr5:64510230
|
A | G | 2 | a0002c0002t0003g0170a0002c0002t0003g0171 | 2 | NA18939.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.332+2353A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64510230 | ||||||
| chr5:64510286
|
A | G | 4 | a0001c0001t0001g0011a0001c0001t0011g0013a0001c0001t0011g0014others(1): Show | 4 | HG02451.hp1 HG03041.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.332+2409A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64510286 | ||||||
| chr5:64510370
|
G | A | 7 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0088others(4): Show | 8 | HG02258.hp1 HG02280.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.332+2493G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64510370 | ||||||
| chr5:64510534
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.332+2657G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64510534 | ||||||
| chr5:64510540
|
G | A | 12 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0093others(9): Show | 13 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.332+2663G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64510540 | ||||||
| chr5:64510920
|
T | A | 81 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0093others(78): Show | 83 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.332+3043T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64510920 | ||||||
| chr5:64510934
|
G | A | 3 | a0001c0001t0001g0021a0001c0001t0002g0020a0001c0001t0010g0019 | 3 | HG00642.hp2 HG01433.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.332+3057G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64510934 | ||||||
| chr5:64511196
|
G | T | 1 | a0001c0001t0004g0084 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.332+3319G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64511196 | ||||||
| chr5:64511251
|
G | A | 108 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0035others(105): Show | 111 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.332+3374G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64511251 | ||||||
| chr5:64511328
|
G | C | 69 | a0001c0001t0001g0194a0001c0001t0001g0214a0001c0001t0001g0237others(66): Show | 70 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.332+3451G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64511328 | ||||||
| chr5:64511329
|
G | A | 2 | a0001c0001t0013g0008a0001c0001t0013g0009 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.332+3452G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64511329 | ||||||
| chr5:64511437
|
T | G | 17 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(14): Show | 17 | HG00642.hp2 HG01175.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.332+3560T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64511437 | ||||||
| chr5:64511513
|
A | G | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG01256.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.332+3636A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64511513 | ||||||
| chr5:64511709
|
A | T | 4 | a0001c0001t0001g0011a0001c0001t0011g0013a0001c0001t0011g0014others(1): Show | 4 | HG02451.hp1 HG03041.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.332+3832A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64511709 | ||||||
| chr5:64511752
|
G | C | 1 | a0001c0001t0004g0036 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.332+3875G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64511752 | ||||||
| chr5:64511852
|
C | T | 2 | a0002c0002t0003g0032a0002c0002t0003g0033 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.332+3975C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64511852 | ||||||
| chr5:64512092
|
G | A | 4 | a0001c0001t0001g0011a0001c0001t0011g0013a0001c0001t0011g0014others(1): Show | 4 | HG02451.hp1 HG03041.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.332+4215G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64512092 | ||||||
| chr5:64512222
|
G | A | 1 | a0002c0002t0001g0172 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.332+4345G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64512222 | ||||||
| chr5:64512380
|
T | A | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.332+4503T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64512380 | ||||||
| chr5:64512398
|
C | T | 1 | a0001c0001t0004g0167 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.332+4521C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64512398 | ||||||
| chr5:64512471
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.332+4594C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64512471 | ||||||
| chr5:64512472
|
G | A | 1 | a0001c0001t0004g0038 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.332+4595G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64512472 | ||||||
| chr5:64512869
|
A | AT | 112 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0093others(109): Show | 113 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.332+4998dupT | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64512869 | |||||
| chr5:64512896
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.332+5019T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64512896 | ||||||
| chr5:64512900
|
T | C | 2 | a0001c0001t0004g0254a0001c0001t0004g0255 | 2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.332+5023T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64512900 | ||||||
| chr5:64512905
|
C | A | 19 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0269others(16): Show | 20 | HG01074.hp2 HG01081.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.332+5028C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64512905 | ||||||
| chr5:64513145
|
A | C | 100 | a0001c0001t0001g0097a0001c0001t0001g0100a0001c0001t0001g0106others(97): Show | 100 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.332+5268A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64513145 | ||||||
| chr5:64513228
|
A | T | 100 | a0001c0001t0001g0097a0001c0001t0001g0100a0001c0001t0001g0106others(97): Show | 100 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.332+5351A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64513228 | ||||||
| chr5:64513341
|
T | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG01256.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.332+5464T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64513341 | ||||||
| chr5:64513348
|
C | T | 1 | a0002c0002t0001g0186 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.332+5471C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64513348 | ||||||
| chr5:64513453
|
G | C | 23 | a0001c0001t0001g0011a0001c0001t0001g0258a0001c0001t0001g0259others(20): Show | 24 | HG01074.hp2 HG01081.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.332+5576G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64513453 | ||||||
| chr5:64513815
|
G | A | 1 | a0001c0001t0002g0241 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.332+5938G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64513815 | ||||||
| chr5:64514001
|
T | C | 1 | a0001c0001t0002g0096 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.332+6124T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64514001 | ||||||
| chr5:64514111
|
T | C | 2 | a0001c0001t0001g0040a0001c0001t0007g0039 | 2 | HG03017.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.332+6234T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64514111 | ||||||
| chr5:64514160
|
T | C | 100 | a0001c0001t0001g0097a0001c0001t0001g0100a0001c0001t0001g0106others(97): Show | 100 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.332+6283T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64514160 | ||||||
| chr5:64514184
|
C | A | 1 | a0001c0001t0004g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.332+6307C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64514184 | ||||||
| chr5:64514187
|
T | C | 69 | a0001c0001t0001g0194a0001c0001t0001g0214a0001c0001t0001g0237others(66): Show | 70 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.332+6310T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64514187 | ||||||
| chr5:64514271
|
CA | C | 16 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0035others(13): Show | 17 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.332+6399delA | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64514271 | |||||
| chr5:64514295
|
G | C | 2 | a0001c0001t0002g0195a0001c0001t0002g0196 | 2 | HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.332+6418G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64514295 | ||||||
| chr5:64514515
|
G | A | 3 | a0001c0001t0001g0174a0001c0001t0002g0173a0001c0001t0002g0175 | 3 | HG02965.hp1 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.332+6638G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64514515 | ||||||
| chr5:64514791
|
T | C | 1 | a0002c0002t0001g0256 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.332+6914T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64514791 | ||||||
| chr5:64514796
|
G | T | 12 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0093others(9): Show | 13 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.332+6919G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64514796 | ||||||
| chr5:64514895
|
A | G | 81 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0093others(78): Show | 83 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.332+7018A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64514895 | ||||||
| chr5:64514952
|
T | C | 1 | a0001c0001t0001g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.332+7075T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64514952 | ||||||
| chr5:64515054
|
A | G | 9 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0002g0002others(6): Show | 10 | HG02258.hp1 HG02280.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.332+7177A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64515054 | ||||||
| chr5:64515085
|
T | C | 1 | a0001c0001t0007g0003 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.332+7208T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64515085 | ||||||
| chr5:64515149
|
A | G | 1 | a0001c0001t0006g0187 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.332+7272A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64515149 | ||||||
| chr5:64515154
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.332+7277G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64515154 | ||||||
| chr5:64515241
|
C | T | 81 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0093others(78): Show | 83 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.332+7364C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64515241 | ||||||
| chr5:64515399
|
C | G | 1 | a0001c0001t0002g0271 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.332+7522C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64515399 | ||||||
| chr5:64515550
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.332+7673G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64515550 | ||||||
| chr5:64515711
|
T | TAC | 8 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0002g0002others(5): Show | 9 | HG01891.hp1 HG02922.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.332+7856_332+7857d others(4): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64515711 | |||||
| chr5:64515711
|
T | TACAC | 18 | a0001c0001t0001g0035a0001c0001t0001g0093a0001c0001t0001g0094others(15): Show | 18 | HG01891.hp2 HG01975.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.332+7854_332+7857d others(6): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64515711 | |||||
| chr5:64515711
|
T | TACACAC | 60 | a0001c0001t0001g0194a0001c0001t0001g0214a0001c0001t0001g0237others(57): Show | 61 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.332+7852_332+7857d others(8): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64515711 | |||||
| chr5:64515735
|
T | C | 65 | a0001c0001t0001g0194a0001c0001t0001g0214a0001c0001t0001g0237others(62): Show | 66 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.332+7858T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64515735 | ||||||
| chr5:64515937
|
C | T | 4 | a0001c0001t0001g0011a0001c0001t0011g0013a0001c0001t0011g0014others(1): Show | 4 | HG02451.hp1 HG03041.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.332+8060C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64515937 | ||||||
| chr5:64516008
|
T | A | 1 | a0001c0001t0004g0099 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.332+8131T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64516008 | ||||||
| chr5:64516104
|
G | A | 12 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0093others(9): Show | 13 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.332+8227G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64516104 | ||||||
| chr5:64516147
|
A | C | 1 | a0001c0001t0002g0166 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.332+8270A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64516147 | ||||||
| chr5:64516305
|
C | A | 67 | a0001c0001t0001g0214a0001c0001t0002g0006a0001c0001t0002g0192others(64): Show | 68 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.332+8428C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64516305 | ||||||
| chr5:64516407
|
C | A | 4 | a0001c0001t0006g0086a0001c0001t0006g0087a0001c0001t0015g0017others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.332+8530C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64516407 | ||||||
| chr5:64516439
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.332+8562G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64516439 | ||||||
| chr5:64516685
|
T | C | 1 | a0002c0002t0003g0042 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.332+8808T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64516685 | ||||||
| chr5:64516893
|
C | A | 1 | a0001c0001t0020g0101 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.332+9016C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64516893 | ||||||
| chr5:64516921
|
G | A | 9 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0093others(6): Show | 10 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.332+9044G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64516921 | ||||||
| chr5:64517006
|
T | G | 9 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0093others(6): Show | 10 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.332+9129T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64517006 | ||||||
| chr5:64517016
|
G | GA | 20 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0093others(17): Show | 21 | HG01109.hp1 HG01891.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.332+9158dupA | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64517016 | |||||
| chr5:64517016
|
GA | G | 8 | a0001c0001t0002g0165a0001c0001t0004g0083a0001c0001t0004g0235others(5): Show | 8 | HG00639.hp2 HG01167.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.332+9158delA | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64517016 | |||||
| chr5:64517017
|
A | G | 1 | a0001c0001t0021g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.332+9140A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64517017 | ||||||
| chr5:64517131
|
G | A | 1 | a0001c0001t0002g0045 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.332+9254G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64517131 | ||||||
| chr5:64517569
|
T | C | 101 | a0001c0001t0001g0046a0001c0001t0001g0097a0001c0001t0001g0100others(98): Show | 101 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.332+9692T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64517569 | ||||||
| chr5:64517758
|
A | G | 9 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0093others(6): Show | 10 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.332+9881A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64517758 | ||||||
| chr5:64517866
|
G | T | 1 | a0002c0002t0003g0164 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.332+9989G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64517866 | ||||||
| chr5:64517914
|
AT | A | 9 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0093others(6): Show | 10 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.332+10044delT | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64517914 | |||||
| chr5:64517915
|
T | A | 1 | a0001c0001t0002g0104 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.332+10038T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64517915 | ||||||
| chr5:64518045
|
T | C | 75 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0093others(72): Show | 77 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.332+10168T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64518045 | ||||||
| chr5:64518180
|
T | C | 9 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0093others(6): Show | 10 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.332+10303T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64518180 | ||||||
| chr5:64518238
|
T | C | 1 | a0001c0001t0002g0242 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.332+10361T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64518238 | ||||||
| chr5:64518308
|
A | C | 1 | a0001c0001t0001g0082 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.332+10431A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64518308 | ||||||
| chr5:64518353
|
T | TGTG | 3 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0166 | 3 | NA18965.hp1 NA18981.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.332+10487_332+1048 others(7): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64518353 | |||||
| chr5:64518403
|
AAG | A | 9 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0093others(6): Show | 10 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.332+10531_332+1053 others(6): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64518403 | |||||
| chr5:64518421
|
G | A | 1 | a0002c0002t0003g0105 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.332+10544G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64518421 | ||||||
| chr5:64518435
|
G | A | 35 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0023others(32): Show | 35 | HG00642.hp2 HG01109.hp1 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.332+10558G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64518435 | ||||||
| chr5:64518453
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.332+10576T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64518453 | ||||||
| chr5:64518648
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.332+10771G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64518648 | ||||||
| chr5:64518770
|
A | G | 3 | a0001c0001t0001g0040a0001c0001t0007g0039a0002c0002t0003g0081 | 3 | HG01123.hp2 HG03017.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.332+10893A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64518770 | ||||||
| chr5:64518851
|
C | G | 1 | a0001c0001t0002g0231 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.332+10974C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64518851 | ||||||
| chr5:64519500
|
C | A | 116 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0046others(113): Show | 116 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.332+11623C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64519500 | ||||||
| chr5:64519502
|
A | G | 4 | a0001c0001t0008g0007a0001c0001t0013g0008a0001c0001t0013g0009others(1): Show | 4 | HG01891.hp2 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.332+11625A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64519502 | ||||||
| chr5:64519511
|
G | A | 4 | a0001c0001t0006g0086a0001c0001t0006g0087a0001c0001t0015g0017others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.332+11634G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64519511 | ||||||
| chr5:64519586
|
T | A | 2 | a0001c0001t0001g0194a0001c0001t0001g0237 | 2 | HG02055.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.332+11709T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64519586 | ||||||
| chr5:64519631
|
T | C | 117 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0046others(114): Show | 117 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.332+11754T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64519631 | ||||||
| chr5:64519632
|
T | A | 1 | a0001c0001t0002g0165 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.332+11755T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64519632 | ||||||
| chr5:64519698
|
G | A | 2 | a0001c0001t0001g0106a0002c0002t0003g0107 | 2 | NA18950.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.332+11821G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64519698 | ||||||
| chr5:64519770
|
G | A | 2 | a0001c0001t0001g0194a0001c0001t0001g0237 | 2 | HG02055.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.332+11893G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64519770 | ||||||
| chr5:64519808
|
T | C | 189 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(186): Show | 189 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.332+11931T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64519808 | ||||||
| chr5:64519903
|
G | C | 2 | a0001c0001t0013g0008a0001c0001t0013g0009 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.332+12026G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64519903 | ||||||
| chr5:64519922
|
C | T | 1 | a0002c0002t0003g0161 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.332+12045C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64519922 | ||||||
| chr5:64519954
|
T | A | 3 | a0001c0001t0004g0254a0001c0001t0004g0255a0001c0001t0008g0257 | 3 | HG01109.hp1 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.332+12077T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64519954 | ||||||
| chr5:64519991
|
G | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0052a0001c0001t0011g0013others(2): Show | 5 | HG02451.hp1 HG03041.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.332+12114G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64519991 | ||||||
| chr5:64520166
|
T | G | 53 | a0001c0001t0001g0214a0001c0001t0002g0006a0001c0001t0002g0192others(50): Show | 53 | HG00558.hp1 HG00639.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.332+12289T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64520166 | ||||||
| chr5:64520257
|
G | T | 1 | a0001c0001t0019g0226 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.332+12380G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64520257 | ||||||
| chr5:64520363
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.332+12486C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64520363 | ||||||
| chr5:64520521
|
C | T | 3 | a0001c0001t0001g0194a0001c0001t0001g0237a0001c0001t0002g0240 | 3 | HG02055.hp1 HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.332+12644C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64520521 | ||||||
| chr5:64520522
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0009g0054 | 2 | HG02055.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.332+12645G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64520522 | ||||||
| chr5:64520779
|
A | G | 2 | a0001c0001t0006g0086a0001c0001t0006g0087 | 2 | HG02257.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.332+12902A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64520779 | ||||||
| chr5:64521089
|
G | A | 3 | a0001c0001t0001g0055a0001c0001t0007g0003a0001c0001t0007g0056 | 4 | HG03491.hp2 HG03492.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.332+13212G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64521089 | ||||||
| chr5:64521247
|
T | C | 1 | a0001c0001t0004g0274 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.332+13370T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64521247 | ||||||
| chr5:64521315
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.332+13438C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64521315 | ||||||
| chr5:64521319
|
G | A | 9 | a0001c0001t0001g0034a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 10 | HG01891.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.332+13442G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64521319 | ||||||
| chr5:64521406
|
G | A | 3 | a0001c0001t0001g0194a0001c0001t0001g0237a0001c0001t0002g0240 | 3 | HG02055.hp1 HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.332+13529G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64521406 | ||||||
| chr5:64521908
|
C | T | 53 | a0001c0001t0001g0214a0001c0001t0002g0006a0001c0001t0002g0192others(50): Show | 53 | HG00558.hp1 HG00639.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.332+14031C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64521908 | ||||||
| chr5:64522201
|
G | T | 2 | a0001c0001t0005g0190a0002c0002t0003g0191 | 2 | NA18951.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.332+14324G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64522201 | ||||||
| chr5:64522223
|
C | G | 3 | a0001c0001t0013g0008a0001c0001t0013g0009a0001c0001t0021g0010 | 3 | HG02647.hp1 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.332+14346C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64522223 | ||||||
| chr5:64522299
|
A | G | 3 | a0001c0001t0004g0254a0001c0001t0004g0255a0001c0001t0008g0257 | 3 | HG01109.hp1 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.332+14422A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64522299 | ||||||
| chr5:64522659
|
T | A | 1 | a0001c0001t0001g0108 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.332+14782T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64522659 | ||||||
| chr5:64522905
|
C | T | 53 | a0001c0001t0001g0214a0001c0001t0002g0006a0001c0001t0002g0192others(50): Show | 53 | HG00558.hp1 HG00639.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.332+15028C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64522905 | ||||||
| chr5:64522987
|
A | T | 3 | a0001c0001t0004g0235a0001c0001t0004g0236a0002c0002t0001g0234 | 3 | HG01256.hp1 HG01258.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.332+15110A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64522987 | ||||||
| chr5:64523255
|
C | T | 1 | a0001c0001t0006g0187 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.332+15378C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64523255 | ||||||
| chr5:64523293
|
A | T | 9 | a0001c0001t0001g0034a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 10 | HG01891.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.332+15416A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64523293 | ||||||
| chr5:64523336
|
A | AT | 76 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0029others(73): Show | 76 | HG00558.hp1 HG00639.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.332+15468dupT | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64523336 | |||||
| chr5:64523353
|
C | T | 1 | a0002c0002t0006g0085 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.332+15476C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64523353 | ||||||
| chr5:64523372
|
A | G | 1 | a0001c0001t0004g0036 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.332+15495A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64523372 | ||||||
| chr5:64523411
|
A | G | 6 | a0001c0001t0002g0160a0001c0001t0004g0158a0001c0001t0004g0167others(3): Show | 6 | HG00423.hp2 HG02015.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.332+15534A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64523411 | ||||||
| chr5:64523529
|
A | C | 1 | a0002c0002t0003g0193 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.332+15652A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64523529 | ||||||
| chr5:64523643
|
G | C | 1 | a0001c0001t0002g0230 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.332+15766G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64523643 | ||||||
| chr5:64523688
|
T | C | 1 | a0001c0001t0006g0187 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.332+15811T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64523688 | ||||||
| chr5:64523807
|
G | A | 3 | a0001c0001t0004g0235a0001c0001t0004g0236a0002c0002t0001g0234 | 3 | HG01256.hp1 HG01258.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.332+15930G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64523807 | ||||||
| chr5:64523832
|
C | T | 1 | a0002c0002t0003g0163 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.332+15955C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64523832 | ||||||
| chr5:64523942
|
A | G | 1 | a0001c0001t0002g0044 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.332+16065A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64523942 | ||||||
| chr5:64524004
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0052a0001c0001t0011g0013others(2): Show | 5 | HG02451.hp1 HG03041.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.332+16127C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64524004 | ||||||
| chr5:64524082
|
T | A | 1 | a0001c0001t0004g0037 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.332+16205T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64524082 | ||||||
| chr5:64524239
|
C | T | 213 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(210): Show | 214 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(211): Show |
intron_variant | MODIFIER | c.332+16362C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64524239 | ||||||
| chr5:64524292
|
G | A | 95 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0046others(92): Show | 95 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.332+16415G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64524292 | ||||||
| chr5:64524377
|
A | C | 5 | a0002c0002t0001g0172a0002c0002t0001g0182a0002c0002t0001g0183others(2): Show | 5 | HG01167.hp1 HG01884.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.332+16500A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64524377 | ||||||
| chr5:64524380
|
G | C | 204 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(201): Show | 205 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.332+16503G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64524380 | ||||||
| chr5:64524631
|
A | G | 4 | a0001c0001t0006g0086a0001c0001t0006g0087a0001c0001t0015g0017others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.332+16754A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64524631 | ||||||
| chr5:64524949
|
C | T | 8 | a0001c0001t0006g0086a0001c0001t0006g0087a0001c0001t0008g0007others(5): Show | 8 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.332+17072C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64524949 | ||||||
| chr5:64525065
|
T | C | 1 | a0001c0001t0008g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.332+17188T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64525065 | ||||||
| chr5:64525162
|
C | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0076others(2): Show | 7 | HG02615.hp1 HG02647.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.332+17285C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64525162 | ||||||
| chr5:64525164
|
G | A | 1 | a0001c0001t0002g0205 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.332+17287G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64525164 | ||||||
| chr5:64525244
|
T | C | 3 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0166 | 3 | NA18965.hp1 NA18981.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.332+17367T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64525244 | ||||||
| chr5:64525301
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.332+17424G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64525301 | ||||||
| chr5:64525345
|
C | G | 1 | a0001c0001t0009g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.332+17468C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64525345 | ||||||
| chr5:64525403
|
T | C | 4 | a0001c0001t0006g0086a0001c0001t0006g0087a0001c0001t0015g0017others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.332+17526T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64525403 | ||||||
| chr5:64525490
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.332+17613G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64525490 | ||||||
| chr5:64525501
|
T | C | 9 | a0001c0001t0001g0034a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 10 | HG01891.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.332+17624T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64525501 | ||||||
| chr5:64525519
|
A | G | 1 | a0002c0002t0003g0156 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.332+17642A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64525519 | ||||||
| chr5:64525588
|
G | A | 5 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0004g0254others(2): Show | 5 | HG01109.hp1 HG02559.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.332+17711G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64525588 | ||||||
| chr5:64526106
|
C | T | 1 | a0001c0001t0002g0270 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.332+18229C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64526106 | ||||||
| chr5:64526107
|
G | A | 1 | a0002c0002t0001g0232 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.332+18230G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64526107 | ||||||
| chr5:64526188
|
G | A | 1 | a0001c0001t0020g0101 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.332+18311G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64526188 | ||||||
| chr5:64526284
|
A | G | 4 | a0001c0001t0004g0203a0002c0002t0003g0105a0002c0002t0003g0154others(1): Show | 4 | HG00597.hp1 HG00621.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.332+18407A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64526284 | ||||||
| chr5:64526412
|
C | T | 2 | a0001c0001t0001g0047a0001c0001t0001g0080 | 2 | HG00738.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.332+18535C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64526412 | ||||||
| chr5:64526493
|
C | A | 2 | a0002c0002t0003g0032a0002c0002t0003g0033 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.332+18616C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64526493 | ||||||
| chr5:64526600
|
A | G | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.332+18723A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64526600 | ||||||
| chr5:64526610
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.332+18733A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64526610 | ||||||
| chr5:64526816
|
G | A | 1 | a0002c0002t0003g0156 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.332+18939G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64526816 | ||||||
| chr5:64527054
|
C | T | 1 | a0001c0001t0002g0153 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.332+19177C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64527054 | ||||||
| chr5:64527207
|
G | A | 6 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0002g0002others(3): Show | 7 | HG02258.hp1 HG03098.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.332+19330G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64527207 | ||||||
| chr5:64527221
|
A | C | 4 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0225others(1): Show | 4 | HG02602.hp1 HG02738.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.332+19344A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64527221 | ||||||
| chr5:64527265
|
C | G | 200 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(197): Show | 200 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.332+19388C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64527265 | ||||||
| chr5:64527441
|
G | A | 4 | a0001c0001t0006g0086a0001c0001t0006g0087a0001c0001t0015g0017others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.332+19564G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64527441 | ||||||
| chr5:64527532
|
C | T | 13 | a0001c0001t0001g0174a0001c0001t0001g0177a0001c0001t0002g0043others(10): Show | 13 | HG01167.hp1 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.332+19655C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64527532 | ||||||
| chr5:64527556
|
T | C | 5 | a0001c0001t0001g0074a0001c0001t0008g0007a0001c0001t0013g0008others(2): Show | 5 | HG01891.hp2 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.332+19679T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64527556 | ||||||
| chr5:64527606
|
T | TA | 18 | a0001c0001t0001g0001a0001c0001t0001g0047a0001c0001t0001g0057others(15): Show | 20 | HG00738.hp1 HG01081.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.332+19765dupA | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64527606 | |||||
| chr5:64527606
|
TAAAAAAA others(3): Show |
T | 1 | a0001c0001t0004g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.332+19756_332+1976 others(14): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64527606 | |||||
| chr5:64527606
|
TAAAAAAA others(4): Show |
T | 2 | a0001c0001t0001g0194a0001c0001t0015g0017 | 2 | HG01884.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.332+19755_332+1976 others(15): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64527606 | |||||
| chr5:64527606
|
TAAAAAAA others(5): Show |
T | 7 | a0001c0001t0001g0237a0001c0001t0002g0240a0001c0001t0004g0037others(4): Show | 7 | HG02257.hp1 HG02572.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.332+19754_332+1976 others(16): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64527606 | |||||
| chr5:64527606
|
TAAAAAAA others(6): Show |
T | 20 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0035others(17): Show | 20 | HG00558.hp1 HG00642.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.332+19753_332+1976 others(17): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64527606 | |||||
| chr5:64527606
|
TAAAAAAA others(7): Show |
T | 150 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0046others(147): Show | 150 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.332+19752_332+1976 others(18): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64527606 | |||||
| chr5:64527606
|
TAAAAAAA others(8): Show |
T | 16 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0152others(13): Show | 16 | HG01071.hp2 HG01167.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.332+19751_332+1976 others(19): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64527606 | |||||
| chr5:64527606
|
TAAAAAAA others(9): Show |
T | 1 | a0002c0002t0001g0185 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.332+19750_332+1976 others(20): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64527606 | |||||
| chr5:64527606
|
TAAAAAAA others(10): Show |
T | 7 | a0001c0001t0001g0034a0001c0001t0001g0093a0001c0001t0001g0094others(4): Show | 8 | HG01891.hp1 HG02258.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.332+19749_332+1976 others(21): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64527606 | |||||
| chr5:64527606
|
TAAAAAAA others(11): Show |
T | 1 | a0001c0001t0004g0036 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.332+19748_332+1976 others(22): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64527606 | |||||
| chr5:64527606
|
TAAAAAAA others(13): Show |
T | 4 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0004g0022others(1): Show | 4 | NA18941.hp2 NA18977.hp2 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.332+19746_332+1976 others(24): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64527606 | |||||
| chr5:64527642
|
A | G | 115 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0046others(112): Show | 115 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.332+19765A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64527642 | ||||||
| chr5:64527713
|
T | C | 9 | a0001c0001t0001g0034a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 10 | HG01891.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.332+19836T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64527713 | ||||||
| chr5:64527728
|
T | G | 1 | a0001c0001t0018g0210 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.332+19851T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64527728 | ||||||
| chr5:64527834
|
C | T | 1 | a0002c0002t0001g0181 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.332+19957C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64527834 | ||||||
| chr5:64527982
|
T | C | 1 | a0002c0002t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.332+20105T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64527982 | ||||||
| chr5:64527985
|
T | C | 1 | a0001c0001t0004g0036 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.332+20108T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64527985 | ||||||
| chr5:64528048
|
C | T | 2 | a0001c0001t0001g0100a0002c0002t0001g0157 | 2 | HG01978.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.332+20171C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64528048 | ||||||
| chr5:64528183
|
G | C | 9 | a0001c0001t0001g0034a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 10 | HG01891.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.332+20306G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64528183 | ||||||
| chr5:64528188
|
A | G | 9 | a0001c0001t0001g0034a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 10 | HG01891.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.332+20311A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64528188 | ||||||
| chr5:64528246
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.332+20369G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64528246 | ||||||
| chr5:64528388
|
A | G | 1 | a0002c0002t0001g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.332+20511A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64528388 | ||||||
| chr5:64528534
|
G | A | 1 | a0002c0002t0003g0081 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.332+20657G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64528534 | ||||||
| chr5:64528609
|
C | T | 1 | a0002c0002t0003g0155 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.332+20732C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64528609 | ||||||
| chr5:64528641
|
G | A | 188 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(185): Show | 188 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.332+20764G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64528641 | ||||||
| chr5:64528709
|
G | A | 1 | a0002c0002t0003g0112 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.332+20832G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64528709 | ||||||
| chr5:64528713
|
C | T | 1 | a0002c0002t0003g0031 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.332+20836C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64528713 | ||||||
| chr5:64528810
|
C | CA | 14 | a0001c0001t0001g0011a0001c0001t0001g0053a0001c0001t0001g0093others(11): Show | 15 | HG01175.hp2 HG02055.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.332+20960dupA | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64528810 | |||||
| chr5:64528810
|
CA | C | 11 | a0001c0001t0001g0047a0001c0001t0001g0052a0001c0001t0002g0195others(8): Show | 12 | HG00738.hp1 HG01081.hp2 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.332+20960delA | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64528810 | |||||
| chr5:64528810
|
CAA | C | 53 | a0001c0001t0001g0214a0001c0001t0001g0258a0001c0001t0001g0259others(50): Show | 53 | HG00558.hp1 HG00639.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.332+20959_332+2096 others(6): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64528810 | |||||
| chr5:64528810
|
CAAA | C | 25 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0029others(22): Show | 25 | HG00597.hp1 HG01109.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.332+20958_332+2096 others(7): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64528810 | |||||
| chr5:64528810
|
CAAAA | C | 114 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0035others(111): Show | 114 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.332+20957_332+2096 others(8): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64528810 | |||||
| chr5:64528810
|
CAAAAA | C | 6 | a0001c0001t0001g0148a0001c0001t0002g0153a0001c0001t0004g0238others(3): Show | 6 | HG01167.hp1 HG01258.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.332+20956_332+2096 others(9): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64528810 | |||||
| chr5:64528819
|
A | C | 1 | a0001c0001t0004g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.332+20942A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64528819 | ||||||
| chr5:64528837
|
A | C | 3 | a0001c0001t0004g0254a0001c0001t0004g0255a0001c0001t0008g0257 | 3 | HG01109.hp1 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.332+20960A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64528837 | ||||||
| chr5:64529086
|
G | A | 1 | a0001c0001t0004g0083 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.332+21209G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64529086 | ||||||
| chr5:64529097
|
A | C | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.332+21220A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64529097 | ||||||
| chr5:64529134
|
G | A | 1 | a0001c0001t0004g0083 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.332+21257G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64529134 | ||||||
| chr5:64529254
|
C | T | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.332+21377C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64529254 | ||||||
| chr5:64529456
|
T | G | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.332+21579T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64529456 | ||||||
| chr5:64529475
|
G | C | 1 | a0001c0001t0001g0063 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.332+21598G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64529475 | ||||||
| chr5:64529476
|
G | C | 219 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0023others(216): Show | 220 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(217): Show |
intron_variant | MODIFIER | c.332+21599G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64529476 | ||||||
| chr5:64529550
|
C | T | 1 | a0001c0001t0015g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.332+21673C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64529550 | ||||||
| chr5:64529594
|
G | C | 1 | a0001c0001t0001g0177 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.332+21717G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64529594 | ||||||
| chr5:64529617
|
G | C | 9 | a0001c0001t0001g0034a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 10 | HG01891.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.332+21740G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64529617 | ||||||
| chr5:64529649
|
A | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0052a0001c0001t0011g0013others(2): Show | 5 | HG02451.hp1 HG03041.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.332+21772A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64529649 | ||||||
| chr5:64529942
|
T | C | 2 | a0002c0002t0003g0206a0002c0002t0003g0207 | 2 | HG00558.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.332+22065T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64529942 | ||||||
| chr5:64530000
|
G | A | 3 | a0001c0001t0001g0194a0001c0001t0001g0237a0001c0001t0002g0240 | 3 | HG02055.hp1 HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.332+22123G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64530000 | ||||||
| chr5:64530053
|
G | C | 1 | a0002c0002t0001g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.332+22176G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64530053 | ||||||
| chr5:64530116
|
G | A | 1 | a0001c0001t0019g0226 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.332+22239G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64530116 | ||||||
| chr5:64530119
|
A | G | 9 | a0001c0001t0001g0034a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 10 | HG01891.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.332+22242A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64530119 | ||||||
| chr5:64530170
|
GA | G | 9 | a0001c0001t0001g0034a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 10 | HG01891.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.332+22301delA | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64530170 | |||||
| chr5:64530356
|
T | C | 95 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0046others(92): Show | 95 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.332+22479T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64530356 | ||||||
| chr5:64530480
|
T | C | 1 | a0001c0001t0002g0114 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.332+22603T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64530480 | ||||||
| chr5:64530762
|
C | CT | 11 | a0001c0001t0001g0034a0001c0001t0001g0093a0001c0001t0001g0094others(8): Show | 12 | HG01891.hp1 HG02258.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.332+22895dupT | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64530762 | |||||
| chr5:64531039
|
G | C | 1 | a0001c0001t0018g0210 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.332+23162G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64531039 | ||||||
| chr5:64531201
|
G | A | 3 | a0001c0001t0001g0194a0001c0001t0001g0237a0001c0001t0002g0240 | 3 | HG02055.hp1 HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.332+23324G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64531201 | ||||||
| chr5:64531352
|
T | A | 9 | a0001c0001t0001g0034a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 10 | HG01891.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.332+23475T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64531352 | ||||||
| chr5:64531381
|
G | A | 219 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0023others(216): Show | 220 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(217): Show |
intron_variant | MODIFIER | c.332+23504G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64531381 | ||||||
| chr5:64531503
|
T | G | 1 | a0002c0002t0003g0062 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.332+23626T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64531503 | ||||||
| chr5:64531518
|
G | A | 1 | a0002c0002t0001g0157 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.332+23641G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64531518 | ||||||
| chr5:64531682
|
T | C | 219 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0023others(216): Show | 220 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(217): Show |
intron_variant | MODIFIER | c.332+23805T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64531682 | ||||||
| chr5:64531745
|
T | C | 1 | a0001c0001t0008g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.332+23868T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64531745 | ||||||
| chr5:64531764
|
C | T | 5 | a0001c0001t0004g0037a0001c0001t0006g0086a0001c0001t0006g0087others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.332+23887C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64531764 | ||||||
| chr5:64532083
|
C | T | 3 | a0002c0002t0001g0221a0002c0002t0001g0222a0002c0002t0001g0232 | 3 | HG01123.hp1 HG03490.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.332+24206C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64532083 | ||||||
| chr5:64532298
|
C | CT | 112 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0046others(109): Show | 112 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.332+24434dupT | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64532298 | |||||
| chr5:64532469
|
G | A | 1 | a0001c0001t0002g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.332+24592G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64532469 | ||||||
| chr5:64532688
|
G | A | 11 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0002g0020others(8): Show | 11 | HG00642.hp2 HG01433.hp1 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.332+24811G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64532688 | ||||||
| chr5:64532787
|
T | G | 1 | a0002c0002t0001g0265 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.332+24910T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64532787 | ||||||
| chr5:64532807
|
A | G | 1 | a0002c0002t0003g0249 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.332+24930A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64532807 | ||||||
| chr5:64532886
|
T | C | 19 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0052others(16): Show | 20 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.332+25009T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64532886 | ||||||
| chr5:64532922
|
C | A | 6 | a0001c0001t0004g0016a0001c0001t0005g0116a0001c0001t0005g0190others(3): Show | 6 | HG02071.hp2 NA18951.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.332+25045C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64532922 | ||||||
| chr5:64533071
|
T | C | 9 | a0001c0001t0001g0034a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 10 | HG01891.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.332+25194T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64533071 | ||||||
| chr5:64533116
|
A | T | 1 | a0002c0002t0003g0193 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.332+25239A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64533116 | ||||||
| chr5:64533220
|
C | A | 9 | a0001c0001t0001g0034a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 10 | HG01891.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.332+25343C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64533220 | ||||||
| chr5:64533499
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.332+25622G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64533499 | ||||||
| chr5:64533523
|
G | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0076others(2): Show | 7 | HG02615.hp1 HG02647.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.332+25646G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64533523 | ||||||
| chr5:64533698
|
T | A | 9 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0258others(6): Show | 10 | HG02258.hp1 HG02280.hp1 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.332+25821T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64533698 | ||||||
| chr5:64533993
|
G | C | 1 | a0001c0001t0002g0192 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.332+26116G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64533993 | ||||||
| chr5:64534028
|
T | C | 2 | a0001c0001t0001g0074a0001c0001t0008g0007 | 2 | HG01891.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.332+26151T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64534028 | ||||||
| chr5:64534140
|
A | G | 1 | a0002c0002t0003g0050 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.332+26263A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64534140 | ||||||
| chr5:64534169
|
C | G | 2 | a0001c0001t0001g0074a0001c0001t0008g0007 | 2 | HG01891.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.332+26292C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64534169 | ||||||
| chr5:64534195
|
T | C | 3 | a0001c0001t0004g0254a0001c0001t0004g0255a0001c0001t0008g0257 | 3 | HG01109.hp1 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.332+26318T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64534195 | ||||||
| chr5:64534241
|
G | A | 219 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0023others(216): Show | 220 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(217): Show |
intron_variant | MODIFIER | c.332+26364G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64534241 | ||||||
| chr5:64534253
|
GGA | G | 80 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0029others(77): Show | 80 | HG00558.hp1 HG00639.hp1 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.332+26378_332+2637 others(6): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64534253 | |||||
| chr5:64534272
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.332+26395G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64534272 | ||||||
| chr5:64534282
|
C | A | 1 | a0001c0001t0002g0230 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.332+26405C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64534282 | ||||||
| chr5:64534307
|
C | T | 4 | a0001c0001t0004g0037a0001c0001t0006g0087a0001c0001t0015g0017others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.332+26430C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64534307 | ||||||
| chr5:64534318
|
T | G | 219 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0023others(216): Show | 220 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(217): Show |
intron_variant | MODIFIER | c.332+26441T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64534318 | ||||||
| chr5:64534383
|
G | T | 1 | a0001c0001t0021g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.332+26506G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64534383 | ||||||
| chr5:64534610
|
G | T | 1 | a0001c0001t0010g0233 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.332+26733G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64534610 | ||||||
| chr5:64534680
|
T | C | 2 | a0002c0002t0003g0032a0002c0002t0003g0033 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.332+26803T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64534680 | ||||||
| chr5:64535056
|
G | A | 75 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0052others(72): Show | 76 | HG00558.hp1 HG00639.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.332+27179G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64535056 | ||||||
| chr5:64535110
|
T | C | 4 | a0001c0001t0005g0116a0001c0001t0005g0190a0001c0001t0005g0272others(1): Show | 4 | NA18951.hp1 NA18986.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.332+27233T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64535110 | ||||||
| chr5:64535128
|
G | A | 9 | a0001c0001t0001g0177a0001c0001t0009g0176a0002c0002t0001g0172others(6): Show | 9 | HG01167.hp1 HG01884.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.332+27251G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64535128 | ||||||
| chr5:64535478
|
C | T | 7 | a0001c0001t0001g0074a0001c0001t0001g0258a0001c0001t0001g0259others(4): Show | 7 | HG01109.hp1 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.332+27601C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64535478 | ||||||
| chr5:64535570
|
A | C | 1 | a0002c0002t0006g0085 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.332+27693A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64535570 | ||||||
| chr5:64535714
|
C | T | 1 | a0002c0002t0003g0062 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.332+27837C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64535714 | ||||||
| chr5:64535748
|
C | G | 1 | a0001c0001t0001g0061 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.332+27871C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64535748 | ||||||
| chr5:64535826
|
T | C | 3 | a0001c0001t0004g0254a0001c0001t0004g0255a0001c0001t0008g0257 | 3 | HG01109.hp1 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.332+27949T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64535826 | ||||||
| chr5:64535863
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.332+27986G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64535863 | ||||||
| chr5:64535968
|
G | C | 57 | a0001c0001t0001g0214a0001c0001t0001g0269a0001c0001t0002g0006others(54): Show | 57 | HG00558.hp1 HG00639.hp1 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.332+28091G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64535968 | ||||||
| chr5:64536099
|
A | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0052a0001c0001t0011g0013others(2): Show | 5 | HG02451.hp1 HG03041.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.332+28222A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64536099 | ||||||
| chr5:64536137
|
T | C | 106 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0046others(103): Show | 106 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.332+28260T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64536137 | ||||||
| chr5:64536217
|
G | A | 3 | a0001c0001t0004g0254a0001c0001t0004g0255a0001c0001t0008g0257 | 3 | HG01109.hp1 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.332+28340G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64536217 | ||||||
| chr5:64536230
|
G | T | 3 | a0001c0001t0004g0254a0001c0001t0004g0255a0001c0001t0008g0257 | 3 | HG01109.hp1 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.332+28353G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64536230 | ||||||
| chr5:64536250
|
T | C | 1 | a0001c0001t0006g0187 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.332+28373T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64536250 | ||||||
| chr5:64536437
|
G | A | 106 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0046others(103): Show | 106 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.332+28560G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64536437 | ||||||
| chr5:64536477
|
A | G | 3 | a0001c0001t0004g0254a0001c0001t0004g0255a0001c0001t0008g0257 | 3 | HG01109.hp1 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.332+28600A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64536477 | ||||||
| chr5:64536578
|
T | C | 1 | a0001c0001t0002g0192 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.332+28701T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64536578 | ||||||
| chr5:64536596
|
T | C | 57 | a0001c0001t0001g0214a0001c0001t0001g0269a0001c0001t0002g0006others(54): Show | 57 | HG00558.hp1 HG00639.hp1 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.332+28719T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64536596 | ||||||
| chr5:64536683
|
C | T | 10 | a0001c0001t0001g0011a0001c0001t0001g0052a0001c0001t0001g0074others(7): Show | 10 | HG01109.hp1 HG01891.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.332+28806C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64536683 | ||||||
| chr5:64536988
|
G | A | 4 | a0001c0001t0004g0037a0001c0001t0006g0087a0001c0001t0015g0017others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.332+29111G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64536988 | ||||||
| chr5:64537311
|
T | C | 106 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0046others(103): Show | 106 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.332+29434T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64537311 | ||||||
| chr5:64537356
|
G | A | 12 | a0001c0001t0001g0011a0001c0001t0001g0052a0001c0001t0001g0074others(9): Show | 12 | HG01109.hp1 HG01891.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.332+29479G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64537356 | ||||||
| chr5:64537370
|
C | T | 28 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0029others(25): Show | 28 | HG00423.hp2 HG00642.hp2 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.332+29493C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64537370 | ||||||
| chr5:64537414
|
T | A | 115 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0034others(112): Show | 116 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.332+29537T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64537414 | ||||||
| chr5:64537626
|
G | C | 2 | a0002c0002t0003g0032a0002c0002t0003g0033 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.332+29749G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64537626 | ||||||
| chr5:64537751
|
C | T | 4 | a0001c0001t0004g0037a0001c0001t0006g0087a0001c0001t0015g0017others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.332+29874C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64537751 | ||||||
| chr5:64537800
|
C | T | 5 | a0001c0001t0001g0074a0001c0001t0004g0254a0001c0001t0004g0255others(2): Show | 5 | HG01109.hp1 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.332+29923C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64537800 | ||||||
| chr5:64537954
|
G | C | 4 | a0001c0001t0004g0037a0001c0001t0006g0087a0001c0001t0015g0017others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.332+30077G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64537954 | ||||||
| chr5:64538114
|
A | G | 7 | a0001c0001t0001g0011a0001c0001t0001g0052a0001c0001t0001g0258others(4): Show | 7 | HG02451.hp1 HG03041.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.332+30237A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64538114 | ||||||
| chr5:64538257
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.332+30380T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64538257 | ||||||
| chr5:64538362
|
C | T | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.332+30485C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64538362 | ||||||
| chr5:64538382
|
G | A | 6 | a0001c0001t0004g0016a0001c0001t0005g0116a0001c0001t0005g0190others(3): Show | 6 | HG02071.hp2 NA18951.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.332+30505G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64538382 | ||||||
| chr5:64538485
|
A | AT | 5 | a0001c0001t0001g0074a0001c0001t0004g0254a0001c0001t0004g0255others(2): Show | 5 | HG01109.hp1 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.332+30616dupT | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64538485 | |||||
| chr5:64538491
|
TTTCC | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0052a0001c0001t0001g0258others(4): Show | 7 | HG02451.hp1 HG03041.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.332+30617_332+3062 others(8): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64538491 | |||||
| chr5:64538499
|
T | C | 7 | a0001c0001t0001g0011a0001c0001t0001g0052a0001c0001t0001g0258others(4): Show | 7 | HG02451.hp1 HG03041.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.332+30622T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64538499 | ||||||
| chr5:64538505
|
C | CT | 19 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0001g0060others(16): Show | 19 | HG00642.hp1 HG01361.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.332+30639dupT | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64538505 | |||||
| chr5:64538505
|
CT | C | 12 | a0001c0001t0001g0011a0001c0001t0001g0052a0001c0001t0001g0074others(9): Show | 12 | HG01891.hp2 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.332+30639delT | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64538505 | |||||
| chr5:64538522
|
TCTTTTCT others(11): Show |
T | 1 | a0002c0002t0006g0085 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.332+30663_332+3068 others(22): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64538522 | |||||
| chr5:64538523
|
CTTTTCTT others(18): Show |
C | 1 | a0001c0001t0018g0210 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.332+30651_332+3067 others(29): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64538523 | |||||
| chr5:64538528
|
C | CT | 119 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0024others(116): Show | 119 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.332+30662dupT | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64538528 | |||||
| chr5:64538546
|
C | CT | 31 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(28): Show | 34 | HG00423.hp2 HG01081.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.332+30697dupT | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64538546 | |||||
| chr5:64538546
|
C | CTT | 79 | a0001c0001t0001g0023a0001c0001t0001g0046a0001c0001t0001g0106others(76): Show | 79 | HG00099.hp2 HG00597.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.332+30696_332+3069 others(6): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64538546 | |||||
| chr5:64538546
|
C | CTTT | 23 | a0001c0001t0001g0024a0001c0001t0001g0111a0001c0001t0001g0113others(20): Show | 23 | HG00423.hp1 HG00558.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.332+30695_332+3069 others(7): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64538546 | |||||
| chr5:64538546
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0001g0259a0001c0001t0011g0013 | 2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.332+30688_332+3069 others(14): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64538546 | |||||
| chr5:64538546
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0011g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.332+30687_332+3069 others(15): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64538546 | |||||
| chr5:64538546
|
C | CTTTTTTT others(5): Show |
1 | a0002c0002t0001g0012 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.332+30686_332+3069 others(16): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64538546 | |||||
| chr5:64538546
|
C | CTTTTTTT others(6): Show |
2 | a0001c0001t0001g0011a0001c0001t0001g0052 | 2 | HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.332+30685_332+3069 others(17): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64538546 | |||||
| chr5:64538546
|
C | T | 1 | a0002c0002t0006g0085 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.332+30669C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64538546 | ||||||
| chr5:64538546
|
CT | C | 14 | a0001c0001t0001g0074a0001c0001t0002g0018a0001c0001t0002g0205others(11): Show | 14 | HG00639.hp2 HG01257.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.332+30697delT | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64538546 | |||||
| chr5:64538546
|
CTT | C | 45 | a0001c0001t0001g0214a0001c0001t0001g0269a0001c0001t0002g0006others(42): Show | 45 | HG00558.hp1 HG00639.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.332+30696_332+3069 others(6): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64538546 | |||||
| chr5:64538646
|
C | T | 12 | a0001c0001t0001g0011a0001c0001t0001g0052a0001c0001t0001g0074others(9): Show | 12 | HG01109.hp1 HG01891.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.332+30769C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64538646 | ||||||
| chr5:64538684
|
G | A | 9 | a0001c0001t0001g0034a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 10 | HG01891.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.332+30807G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64538684 | ||||||
| chr5:64538705
|
CGCACCAT others(5): Show |
C | 3 | a0001c0001t0001g0021a0001c0001t0002g0020a0001c0001t0010g0019 | 3 | HG00642.hp2 HG01433.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.332+30831_332+3084 others(16): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64538705 | |||||
| chr5:64538726
|
T | C | 2 | a0001c0001t0001g0074a0001c0001t0008g0007 | 2 | HG01891.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.332+30849T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64538726 | ||||||
| chr5:64538736
|
A | G | 3 | a0001c0001t0004g0254a0001c0001t0004g0255a0001c0001t0008g0257 | 3 | HG01109.hp1 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.332+30859A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64538736 | ||||||
| chr5:64538936
|
A | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0052a0001c0001t0001g0258others(4): Show | 7 | HG02451.hp1 HG03041.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.332+31059A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64538936 | ||||||
| chr5:64539002
|
T | C | 1 | a0001c0001t0007g0039 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.332+31125T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64539002 | ||||||
| chr5:64539110
|
C | T | 8 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0002g0002others(5): Show | 9 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.332+31233C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64539110 | ||||||
| chr5:64539117
|
CT | C | 5 | a0001c0001t0001g0011a0001c0001t0001g0052a0001c0001t0011g0013others(2): Show | 5 | HG02451.hp1 HG03041.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.332+31241delT | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64539117 | ||||||
| chr5:64539126
|
C | T | 1 | a0001c0001t0005g0272 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.332+31249C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64539126 | ||||||
| chr5:64539353
|
G | C | 7 | a0001c0001t0001g0011a0001c0001t0001g0052a0001c0001t0001g0258others(4): Show | 7 | HG02451.hp1 HG03041.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.332+31476G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64539353 | ||||||
| chr5:64539569
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.332+31692A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64539569 | ||||||
| chr5:64539667
|
C | T | 1 | a0001c0001t0004g0036 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.332+31790C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64539667 | ||||||
| chr5:64539674
|
G | A | 1 | a0001c0001t0005g0272 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.332+31797G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64539674 | ||||||
| chr5:64539773
|
G | C | 4 | a0001c0001t0001g0034a0001c0001t0004g0254a0001c0001t0004g0255others(1): Show | 4 | HG01109.hp1 HG01891.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.332+31896G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64539773 | ||||||
| chr5:64539982
|
T | A | 6 | a0001c0001t0001g0011a0001c0001t0001g0052a0001c0001t0011g0013others(3): Show | 6 | HG02451.hp1 HG03041.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.332+32105T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64539982 | ||||||
| chr5:64540198
|
A | G | 57 | a0001c0001t0001g0214a0001c0001t0001g0269a0001c0001t0002g0006others(54): Show | 57 | HG00558.hp1 HG00639.hp1 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.332+32321A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64540198 | ||||||
| chr5:64540286
|
T | A | 1 | a0001c0001t0015g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.332+32409T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64540286 | ||||||
| chr5:64540562
|
C | T | 57 | a0001c0001t0001g0214a0001c0001t0001g0269a0001c0001t0002g0006others(54): Show | 57 | HG00558.hp1 HG00639.hp1 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.332+32685C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64540562 | ||||||
| chr5:64540583
|
G | A | 1 | a0001c0001t0006g0087 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.332+32706G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64540583 | ||||||
| chr5:64540596
|
C | T | 6 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0002g0002others(3): Show | 7 | HG02258.hp1 HG03098.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.332+32719C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64540596 | ||||||
| chr5:64540785
|
G | A | 56 | a0001c0001t0001g0214a0001c0001t0001g0269a0001c0001t0002g0006others(53): Show | 56 | HG00558.hp1 HG00639.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.332+32908G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64540785 | ||||||
| chr5:64540882
|
T | A | 69 | a0001c0001t0001g0011a0001c0001t0001g0052a0001c0001t0001g0074others(66): Show | 69 | HG00558.hp1 HG00639.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.332+33005T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64540882 | ||||||
| chr5:64541444
|
C | T | 26 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0029others(23): Show | 26 | HG00423.hp2 HG00642.hp2 HG01433.hp1 others(23): Show |
intron_variant | MODIFIER | c.332+33567C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64541444 | ||||||
| chr5:64541445
|
G | A | 1 | a0001c0001t0006g0087 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.332+33568G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64541445 | ||||||
| chr5:64541600
|
G | T | 1 | a0002c0002t0006g0085 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.332+33723G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64541600 | ||||||
| chr5:64541930
|
A | G | 4 | a0001c0001t0001g0060a0002c0002t0003g0071a0002c0002t0003g0073others(1): Show | 4 | NA18965.hp2 NA18998.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.333-33844A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64541930 | ||||||
| chr5:64541951
|
A | G | 1 | a0001c0001t0002g0104 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.333-33823A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64541951 | ||||||
| chr5:64541952
|
G | GT | 184 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0024others(181): Show | 185 | HG00099.hp2 HG00423.hp1 HG00558.hp1 others(182): Show |
intron_variant | MODIFIER | c.333-33814dupT | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64541952 | |||||
| chr5:64542002
|
A | T | 1 | a0001c0001t0001g0070 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.333-33772A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64542002 | ||||||
| chr5:64542011
|
T | A | 69 | a0001c0001t0001g0011a0001c0001t0001g0052a0001c0001t0001g0074others(66): Show | 69 | HG00558.hp1 HG00639.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.333-33763T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64542011 | ||||||
| chr5:64542047
|
G | A | 2 | a0001c0001t0001g0074a0001c0001t0008g0007 | 2 | HG01891.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.333-33727G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64542047 | ||||||
| chr5:64542076
|
C | G | 1 | a0001c0001t0004g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.333-33698C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64542076 | ||||||
| chr5:64542266
|
C | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0052a0001c0001t0001g0258others(4): Show | 7 | HG02451.hp1 HG03041.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.333-33508C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64542266 | ||||||
| chr5:64542285
|
C | G | 7 | a0001c0001t0001g0011a0001c0001t0001g0052a0001c0001t0001g0258others(4): Show | 7 | HG02451.hp1 HG03041.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.333-33489C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64542285 | ||||||
| chr5:64542602
|
A | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0052a0001c0001t0001g0258others(4): Show | 7 | HG02451.hp1 HG03041.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.333-33172A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64542602 | ||||||
| chr5:64542654
|
T | G | 3 | a0001c0001t0004g0254a0001c0001t0004g0255a0001c0001t0008g0257 | 3 | HG01109.hp1 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.333-33120T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64542654 | ||||||
| chr5:64542672
|
C | T | 1 | a0001c0001t0004g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.333-33102C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64542672 | ||||||
| chr5:64542680
|
T | C | 7 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0002g0002others(4): Show | 8 | HG02258.hp1 HG02280.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.333-33094T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64542680 | ||||||
| chr5:64542698
|
G | C | 7 | a0001c0001t0001g0011a0001c0001t0001g0052a0001c0001t0001g0258others(4): Show | 7 | HG02451.hp1 HG03041.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.333-33076G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64542698 | ||||||
| chr5:64542832
|
C | T | 3 | a0001c0001t0013g0008a0001c0001t0013g0009a0001c0001t0021g0010 | 3 | HG02647.hp1 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.333-32942C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64542832 | ||||||
| chr5:64542901
|
G | A | 3 | a0001c0001t0004g0254a0001c0001t0004g0255a0001c0001t0008g0257 | 3 | HG01109.hp1 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.333-32873G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64542901 | ||||||
| chr5:64543037
|
C | T | 3 | a0001c0001t0002g0209a0002c0002t0003g0206a0002c0002t0003g0207 | 3 | HG00558.hp1 NA19070.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.333-32737C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64543037 | ||||||
| chr5:64543499
|
A | C | 3 | a0001c0001t0001g0194a0001c0001t0001g0237a0001c0001t0002g0240 | 3 | HG02055.hp1 HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.333-32275A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64543499 | ||||||
| chr5:64543542
|
T | TA | 112 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0046others(109): Show | 112 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.333-32223dupA | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64543542 | |||||
| chr5:64543750
|
C | A | 1 | a0001c0001t0004g0036 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.333-32024C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64543750 | ||||||
| chr5:64543823
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.333-31951A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64543823 | ||||||
| chr5:64544031
|
G | A | 17 | a0001c0001t0001g0174a0001c0001t0001g0177a0001c0001t0001g0178others(14): Show | 17 | HG01167.hp1 HG01884.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.333-31743G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64544031 | ||||||
| chr5:64544166
|
C | T | 1 | a0001c0001t0004g0084 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.333-31608C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64544166 | ||||||
| chr5:64544214
|
C | T | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.333-31560C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64544214 | ||||||
| chr5:64544358
|
T | G | 2 | a0001c0001t0001g0074a0001c0001t0008g0007 | 2 | HG01891.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.333-31416T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64544358 | ||||||
| chr5:64544381
|
A | C | 106 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0046others(103): Show | 106 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.333-31393A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64544381 | ||||||
| chr5:64544500
|
C | T | 4 | a0001c0001t0001g0035a0001c0001t0013g0008a0001c0001t0013g0009others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.333-31274C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64544500 | ||||||
| chr5:64544510
|
GA | G | 149 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(146): Show | 150 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.333-31249delA | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64544510 | |||||
| chr5:64544510
|
GAA | G | 7 | a0001c0001t0001g0074a0001c0001t0004g0254a0001c0001t0004g0255others(4): Show | 7 | HG01109.hp1 HG01891.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.333-31250_333-3124 others(6): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64544510 | |||||
| chr5:64544519
|
A | G | 108 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0046others(105): Show | 108 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.333-31255A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64544519 | ||||||
| chr5:64544649
|
G | T | 59 | a0001c0001t0001g0214a0001c0001t0001g0269a0001c0001t0002g0006others(56): Show | 59 | HG00558.hp1 HG00639.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.333-31125G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64544649 | ||||||
| chr5:64544675
|
TAAG | T | 26 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0029others(23): Show | 26 | HG00423.hp2 HG00642.hp2 HG01433.hp1 others(23): Show |
intron_variant | MODIFIER | c.333-31087_333-3108 others(7): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64544675 | |||||
| chr5:64544773
|
G | A | 7 | a0001c0001t0001g0046a0001c0001t0001g0097a0001c0001t0001g0108others(4): Show | 7 | HG00741.hp2 HG02486.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.333-31001G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64544773 | ||||||
| chr5:64544836
|
A | T | 1 | a0001c0001t0007g0056 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.333-30938A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64544836 | ||||||
| chr5:64545115
|
G | T | 1 | a0001c0001t0019g0226 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.333-30659G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64545115 | ||||||
| chr5:64545177
|
GA | G | 7 | a0001c0001t0001g0074a0001c0001t0002g0002a0001c0001t0002g0018others(4): Show | 8 | HG01891.hp2 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.333-30583delA | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64545177 | |||||
| chr5:64545252
|
C | T | 1 | a0001c0001t0008g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.333-30522C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64545252 | ||||||
| chr5:64545324
|
T | G | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.333-30450T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64545324 | ||||||
| chr5:64545379
|
T | C | 3 | a0001c0001t0013g0008a0001c0001t0013g0009a0001c0001t0021g0010 | 3 | HG02647.hp1 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.333-30395T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64545379 | ||||||
| chr5:64545397
|
A | G | 1 | a0001c0001t0011g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.333-30377A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64545397 | ||||||
| chr5:64545416
|
TA | T | 5 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0088others(2): Show | 6 | HG02258.hp1 HG03098.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.333-30347delA | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64545416 | |||||
| chr5:64545433
|
G | A | 1 | a0001c0001t0002g0213 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.333-30341G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64545433 | ||||||
| chr5:64545514
|
G | C | 3 | a0001c0001t0004g0016a0001c0001t0005g0123a0002c0002t0003g0110 | 3 | HG02071.hp2 HG03669.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.333-30260G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64545514 | ||||||
| chr5:64545700
|
C | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0029others(180): Show | 189 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.333-30074C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64545700 | ||||||
| chr5:64545706
|
A | G | 1 | a0001c0001t0004g0254 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.333-30068A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64545706 | ||||||
| chr5:64545711
|
A | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0029others(203): Show | 212 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(209): Show |
intron_variant | MODIFIER | c.333-30063A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64545711 | ||||||
| chr5:64545729
|
T | C | 4 | a0001c0001t0001g0074a0001c0001t0002g0240a0001c0001t0008g0007others(1): Show | 4 | HG01109.hp1 HG01891.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.333-30045T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64545729 | ||||||
| chr5:64545884
|
C | G | 1 | a0001c0001t0001g0053 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.333-29890C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64545884 | ||||||
| chr5:64546015
|
G | A | 59 | a0001c0001t0001g0074a0001c0001t0001g0174a0001c0001t0001g0214others(56): Show | 59 | HG00738.hp2 HG01074.hp1 HG01081.hp1 others(56): Show |
intron_variant | MODIFIER | c.333-29759G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64546015 | ||||||
| chr5:64546034
|
G | A | 26 | a0001c0001t0001g0021a0001c0001t0001g0178a0001c0001t0001g0188others(23): Show | 26 | HG00423.hp2 HG00642.hp2 HG01433.hp1 others(23): Show |
intron_variant | MODIFIER | c.333-29740G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64546034 | ||||||
| chr5:64546058
|
A | G | 1 | a0001c0001t0002g0240 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.333-29716A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64546058 | ||||||
| chr5:64546254
|
C | T | 3 | a0001c0001t0013g0008a0001c0001t0013g0009a0001c0001t0021g0010 | 3 | HG02647.hp1 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.333-29520C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64546254 | ||||||
| chr5:64546306
|
T | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0029others(210): Show | 219 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(216): Show |
intron_variant | MODIFIER | c.333-29468T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64546306 | ||||||
| chr5:64546327
|
C | CAG | 59 | a0001c0001t0001g0214a0001c0001t0001g0269a0001c0001t0002g0006others(56): Show | 59 | HG00597.hp2 HG00738.hp2 HG01074.hp1 others(56): Show |
intron_variant | MODIFIER | c.333-29443_333-2944 others(6): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64546327 | |||||
| chr5:64546412
|
T | C | 1 | a0002c0002t0003g0249 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.333-29362T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64546412 | ||||||
| chr5:64546509
|
G | C | 5 | a0001c0001t0001g0074a0001c0001t0001g0174a0001c0001t0002g0240others(2): Show | 5 | HG01109.hp1 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.333-29265G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64546509 | ||||||
| chr5:64546679
|
A | AT | 213 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0029others(210): Show | 219 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(216): Show |
intron_variant | MODIFIER | c.333-29086dupT | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64546679 | |||||
| chr5:64546707
|
A | G | 3 | a0001c0001t0013g0008a0001c0001t0013g0009a0001c0001t0021g0010 | 3 | HG02647.hp1 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.333-29067A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64546707 | ||||||
| chr5:64546789
|
A | G | 3 | a0001c0001t0004g0015a0001c0001t0004g0036a0001c0001t0004g0041 | 3 | HG02451.hp2 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.333-28985A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64546789 | ||||||
| chr5:64546897
|
C | T | 1 | a0001c0001t0002g0240 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.333-28877C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64546897 | ||||||
| chr5:64547254
|
G | A | 7 | a0001c0001t0002g0045a0001c0001t0002g0102a0001c0001t0002g0103others(4): Show | 7 | HG00597.hp2 NA18955.hp1 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.333-28520G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64547254 | ||||||
| chr5:64547308
|
C | T | 5 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0088others(2): Show | 6 | HG02258.hp1 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.333-28466C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64547308 | ||||||
| chr5:64547374
|
C | T | 1 | a0001c0001t0002g0045 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.333-28400C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64547374 | ||||||
| chr5:64547383
|
G | A | 5 | a0001c0001t0001g0074a0001c0001t0001g0174a0001c0001t0002g0240others(2): Show | 5 | HG01109.hp1 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.333-28391G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64547383 | ||||||
| chr5:64547671
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.333-28103C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64547671 | ||||||
| chr5:64547677
|
T | G | 1 | a0001c0001t0001g0070 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.333-28097T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64547677 | ||||||
| chr5:64547917
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.333-27857G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64547917 | ||||||
| chr5:64547920
|
A | G | 1 | a0001c0001t0004g0223 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.333-27854A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64547920 | ||||||
| chr5:64548023
|
T | C | 1 | a0002c0002t0001g0182 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.333-27751T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64548023 | ||||||
| chr5:64548088
|
G | A | 64 | a0001c0001t0001g0074a0001c0001t0001g0174a0001c0001t0001g0214others(61): Show | 64 | HG00597.hp2 HG00738.hp2 HG01074.hp1 others(61): Show |
intron_variant | MODIFIER | c.333-27686G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64548088 | ||||||
| chr5:64548161
|
T | C | 1 | a0001c0001t0007g0039 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.333-27613T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64548161 | ||||||
| chr5:64548244
|
G | A | 5 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0088others(2): Show | 6 | HG02258.hp1 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.333-27530G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64548244 | ||||||
| chr5:64548321
|
C | T | 3 | a0001c0001t0001g0035a0001c0001t0004g0254a0001c0001t0004g0255 | 3 | HG02145.hp2 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.333-27453C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64548321 | ||||||
| chr5:64548400
|
G | A | 5 | a0001c0001t0001g0100a0001c0001t0002g0020a0001c0001t0006g0087others(2): Show | 5 | HG01516.hp1 HG01978.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.333-27374G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64548400 | ||||||
| chr5:64548515
|
T | G | 1 | a0002c0002t0003g0249 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.333-27259T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64548515 | ||||||
| chr5:64548578
|
C | T | 5 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0088others(2): Show | 6 | HG02258.hp1 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.333-27196C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64548578 | ||||||
| chr5:64548673
|
A | ATTTTTGT others(227): Show |
1 | a0001c0001t0002g0196 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.333-27088_333-2708 others(238): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64548673 | |||||
| chr5:64548695
|
C | T | 10 | a0001c0001t0001g0177a0001c0001t0009g0176a0001c0001t0015g0017others(7): Show | 10 | HG01167.hp1 HG01884.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.333-27079C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64548695 | ||||||
| chr5:64548705
|
T | C | 1 | a0001c0001t0002g0196 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.333-27069T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64548705 | ||||||
| chr5:64548707
|
A | T | 1 | a0001c0001t0002g0196 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.333-27067A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64548707 | ||||||
| chr5:64548712
|
G | A | 1 | a0001c0001t0002g0196 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.333-27062G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64548712 | ||||||
| chr5:64548727
|
G | A | 1 | a0001c0001t0004g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.333-27047G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64548727 | ||||||
| chr5:64548851
|
C | CT | 9 | a0001c0001t0001g0097a0001c0001t0001g0108a0001c0001t0001g0120others(6): Show | 9 | HG02451.hp1 HG02486.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.333-26907dupT | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64548851 | |||||
| chr5:64548851
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0004g0223 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.333-26917_333-2690 others(15): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64548851 | |||||
| chr5:64548851
|
C | CTTTTTTT others(5): Show |
3 | a0001c0001t0002g0002a0001c0001t0002g0089a0001c0001t0006g0086 | 4 | HG02258.hp1 HG02717.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.333-26918_333-2690 others(16): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64548851 | |||||
| chr5:64548851
|
C | CTTTTTTT others(6): Show |
2 | a0001c0001t0002g0018a0001c0001t0002g0088 | 2 | HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.333-26919_333-2690 others(17): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64548851 | |||||
| chr5:64549179
|
A | G | 60 | a0001c0001t0001g0214a0001c0001t0001g0269a0001c0001t0002g0006others(57): Show | 60 | HG00597.hp2 HG00738.hp2 HG01074.hp1 others(57): Show |
intron_variant | MODIFIER | c.333-26595A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64549179 | ||||||
| chr5:64549316
|
T | C | 1 | a0001c0001t0004g0223 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.333-26458T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64549316 | ||||||
| chr5:64549359
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.333-26415C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64549359 | ||||||
| chr5:64549448
|
G | A | 7 | a0001c0001t0002g0045a0001c0001t0002g0102a0001c0001t0002g0103others(4): Show | 7 | HG00597.hp2 NA18955.hp1 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.333-26326G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64549448 | ||||||
| chr5:64549748
|
A | G | 1 | a0001c0001t0002g0251 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.333-26026A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64549748 | ||||||
| chr5:64549893
|
G | C | 4 | a0001c0001t0001g0100a0001c0001t0006g0087a0001c0001t0011g0014others(1): Show | 4 | HG01978.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.333-25881G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64549893 | ||||||
| chr5:64549941
|
A | G | 60 | a0001c0001t0001g0214a0001c0001t0001g0269a0001c0001t0002g0006others(57): Show | 60 | HG00597.hp2 HG00738.hp2 HG01074.hp1 others(57): Show |
intron_variant | MODIFIER | c.333-25833A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64549941 | ||||||
| chr5:64550063
|
T | A | 1 | a0001c0001t0004g0223 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.333-25711T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64550063 | ||||||
| chr5:64550092
|
T | C | 1 | a0001c0001t0004g0223 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.333-25682T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64550092 | ||||||
| chr5:64550132
|
T | C | 65 | a0001c0001t0001g0074a0001c0001t0001g0174a0001c0001t0001g0214others(62): Show | 65 | HG00597.hp2 HG00738.hp2 HG01074.hp1 others(62): Show |
intron_variant | MODIFIER | c.333-25642T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64550132 | ||||||
| chr5:64550201
|
C | A | 1 | a0001c0001t0004g0139 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.333-25573C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64550201 | ||||||
| chr5:64550460
|
TACCCCAT others(1229): Show |
T | 1 | a0001c0001t0001g0178 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.333-25311_333-2407 others(4): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64550460 | |||||
| chr5:64550466
|
A | G | 4 | a0001c0001t0005g0116a0001c0001t0005g0190a0001c0001t0005g0272others(1): Show | 4 | NA18951.hp1 NA18986.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.333-25308A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64550466 | ||||||
| chr5:64550526
|
G | GAGATAC | 6 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0088others(3): Show | 7 | HG01257.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.333-25247_333-2524 others(10): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64550526 | |||||
| chr5:64550535
|
C | T | 1 | a0001c0001t0004g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.333-25239C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64550535 | ||||||
| chr5:64550566
|
C | A | 6 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0088others(3): Show | 7 | HG01257.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.333-25208C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64550566 | ||||||
| chr5:64550580
|
T | A | 4 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0088others(1): Show | 5 | HG02258.hp1 HG03098.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.333-25194T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64550580 | ||||||
| chr5:64550708
|
C | G | 5 | a0001c0001t0001g0074a0001c0001t0001g0174a0001c0001t0002g0240others(2): Show | 5 | HG01109.hp1 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.333-25066C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64550708 | ||||||
| chr5:64550849
|
C | T | 10 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0194others(7): Show | 10 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.333-24925C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64550849 | ||||||
| chr5:64550930
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.333-24844A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64550930 | ||||||
| chr5:64550955
|
T | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0040others(102): Show | 111 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.333-24819T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64550955 | ||||||
| chr5:64551022
|
A | C | 1 | a0002c0002t0001g0172 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.333-24752A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64551022 | ||||||
| chr5:64551075
|
G | A | 1 | a0002c0002t0001g0012 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.333-24699G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64551075 | ||||||
| chr5:64551096
|
ACAAGTCA others(71): Show |
A | 1 | a0002c0002t0003g0098 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.333-24674_333-2459 others(82): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64551096 | |||||
| chr5:64551118
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.333-24656C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64551118 | ||||||
| chr5:64551247
|
T | A | 4 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0160others(1): Show | 4 | NA18965.hp1 NA18981.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.333-24527T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64551247 | ||||||
| chr5:64551267
|
A | T | 4 | a0001c0001t0001g0100a0001c0001t0006g0087a0001c0001t0011g0014others(1): Show | 4 | HG01978.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.333-24507A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64551267 | ||||||
| chr5:64551403
|
C | A | 1 | a0001c0001t0006g0087 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.333-24371C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64551403 | ||||||
| chr5:64551549
|
G | T | 1 | a0001c0001t0002g0242 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.333-24225G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64551549 | ||||||
| chr5:64551698
|
C | T | 6 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0088others(3): Show | 7 | HG01257.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.333-24076C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64551698 | ||||||
| chr5:64551849
|
C | T | 6 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0088others(3): Show | 7 | HG01257.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.333-23925C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64551849 | ||||||
| chr5:64551870
|
A | G | 6 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0088others(3): Show | 7 | HG01257.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.333-23904A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64551870 | ||||||
| chr5:64551969
|
GCTTGACA others(16): Show |
G | 1 | a0001c0001t0004g0158 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.333-23801_333-2377 others(27): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64551969 | |||||
| chr5:64552025
|
C | T | 1 | a0002c0002t0003g0119 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.333-23749C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64552025 | ||||||
| chr5:64552095
|
C | A | 9 | a0001c0001t0001g0177a0001c0001t0009g0176a0002c0002t0001g0172others(6): Show | 9 | HG01167.hp1 HG01884.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.333-23679C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64552095 | ||||||
| chr5:64552174
|
T | C | 1 | a0001c0001t0004g0274 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.333-23600T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64552174 | ||||||
| chr5:64552270
|
GTTC | G | 6 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0088others(3): Show | 7 | HG01257.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.333-23501_333-2349 others(7): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64552270 | |||||
| chr5:64552456
|
AT | A | 13 | a0001c0001t0001g0178a0001c0001t0001g0188a0001c0001t0001g0189others(10): Show | 13 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.333-23317delT | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64552456 | ||||||
| chr5:64552529
|
G | A | 1 | a0001c0001t0002g0192 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.333-23245G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64552529 | ||||||
| chr5:64552631
|
C | G | 9 | a0001c0001t0001g0177a0001c0001t0009g0176a0002c0002t0001g0172others(6): Show | 9 | HG01167.hp1 HG01884.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.333-23143C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64552631 | ||||||
| chr5:64552673
|
G | A | 4 | a0001c0001t0001g0035a0001c0001t0004g0041a0001c0001t0004g0254others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.333-23101G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64552673 | ||||||
| chr5:64552704
|
G | A | 1 | a0002c0002t0003g0201 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.333-23070G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64552704 | ||||||
| chr5:64553093
|
T | G | 1 | a0001c0001t0004g0223 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.333-22681T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64553093 | ||||||
| chr5:64553171
|
C | CT | 151 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0047others(148): Show | 156 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(153): Show |
intron_variant | MODIFIER | c.333-22584dupT | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64553171 | |||||
| chr5:64553171
|
C | CTT | 10 | a0001c0001t0002g0018a0001c0001t0004g0143a0001c0001t0004g0223others(7): Show | 11 | HG00558.hp2 HG01257.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.333-22585_333-2258 others(6): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64553171 | |||||
| chr5:64553425
|
G | T | 1 | a0002c0002t0003g0112 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.333-22349G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64553425 | ||||||
| chr5:64553853
|
G | T | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.333-21921G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64553853 | ||||||
| chr5:64553993
|
G | T | 1 | a0001c0001t0011g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.333-21781G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64553993 | ||||||
| chr5:64554102
|
C | G | 5 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0088others(2): Show | 6 | HG02258.hp1 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.333-21672C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64554102 | ||||||
| chr5:64554139
|
G | A | 3 | a0001c0001t0002g0213a0001c0001t0002g0216a0002c0002t0003g0098 | 3 | HG02083.hp2 HG04204.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.333-21635G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64554139 | ||||||
| chr5:64554147
|
T | C | 1 | a0002c0002t0001g0185 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.333-21627T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64554147 | ||||||
| chr5:64554283
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.333-21491C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64554283 | ||||||
| chr5:64554330
|
C | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0029others(210): Show | 219 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(216): Show |
intron_variant | MODIFIER | c.333-21444C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64554330 | ||||||
| chr5:64554759
|
T | C | 1 | a0001c0001t0004g0223 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.333-21015T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64554759 | ||||||
| chr5:64554958
|
G | A | 20 | a0001c0001t0001g0034a0001c0001t0001g0178a0001c0001t0001g0188others(17): Show | 20 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.333-20816G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64554958 | ||||||
| chr5:64555052
|
G | A | 1 | a0001c0001t0004g0197 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.333-20722G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64555052 | ||||||
| chr5:64555186
|
A | G | 7 | a0001c0001t0001g0035a0001c0001t0004g0041a0001c0001t0004g0254others(4): Show | 7 | HG02145.hp2 HG02559.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.333-20588A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64555186 | ||||||
| chr5:64555475
|
T | G | 2 | a0001c0001t0002g0115a0002c0002t0003g0224 | 2 | NA18945.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.333-20299T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64555475 | ||||||
| chr5:64555505
|
T | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0047others(91): Show | 99 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.333-20269T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64555505 | ||||||
| chr5:64555595
|
G | T | 1 | a0001c0001t0002g0205 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.333-20179G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64555595 | ||||||
| chr5:64555631
|
A | C | 1 | a0001c0001t0005g0123 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.333-20143A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64555631 | ||||||
| chr5:64555633
|
T | G | 61 | a0001c0001t0001g0214a0001c0001t0001g0269a0001c0001t0002g0006others(58): Show | 61 | HG00597.hp2 HG00738.hp2 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.333-20141T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64555633 | ||||||
| chr5:64555640
|
G | C | 1 | a0002c0002t0001g0262 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.333-20134G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64555640 | ||||||
| chr5:64555742
|
T | C | 1 | a0002c0002t0003g0252 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.333-20032T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64555742 | ||||||
| chr5:64555850
|
T | C | 2 | a0001c0001t0002g0250a0002c0002t0001g0185 | 2 | HG02280.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.333-19924T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64555850 | ||||||
| chr5:64555969
|
T | C | 5 | a0001c0001t0001g0074a0001c0001t0001g0174a0001c0001t0002g0240others(2): Show | 5 | HG01109.hp1 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.333-19805T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64555969 | ||||||
| chr5:64555982
|
G | A | 2 | a0001c0001t0004g0015a0001c0001t0004g0036 | 2 | HG02451.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.333-19792G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64555982 | ||||||
| chr5:64556122
|
A | G | 1 | a0002c0002t0001g0185 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.333-19652A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64556122 | ||||||
| chr5:64556324
|
G | A | 5 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0088others(2): Show | 6 | HG02258.hp1 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.333-19450G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64556324 | ||||||
| chr5:64556327
|
TGAAATGA others(9): Show |
T | 90 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0047others(87): Show | 95 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.333-19426_333-1941 others(20): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64556327 | |||||
| chr5:64556378
|
C | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0029others(210): Show | 219 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(216): Show |
intron_variant | MODIFIER | c.333-19396C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64556378 | ||||||
| chr5:64556387
|
T | TA | 6 | a0001c0001t0001g0052a0001c0001t0002g0002a0001c0001t0002g0018others(3): Show | 7 | HG02258.hp1 HG02717.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.333-19372dupA | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64556387 | |||||
| chr5:64556387
|
TA | T | 70 | a0001c0001t0001g0035a0001c0001t0001g0214a0001c0001t0001g0269others(67): Show | 70 | HG00597.hp2 HG00738.hp2 HG01074.hp1 others(67): Show |
intron_variant | MODIFIER | c.333-19372delA | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64556387 | |||||
| chr5:64556417
|
C | CCA | 43 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0035others(40): Show | 43 | HG00597.hp2 HG00642.hp1 HG01123.hp2 others(40): Show |
intron_variant | MODIFIER | c.333-19314_333-1931 others(6): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64556417 | |||||
| chr5:64556417
|
C | CCACA | 13 | a0001c0001t0001g0055a0001c0001t0001g0269a0001c0001t0002g0192others(10): Show | 13 | HG01109.hp1 HG01975.hp2 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.333-19316_333-1931 others(8): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64556417 | |||||
| chr5:64556417
|
C | CCACACA | 5 | a0001c0001t0002g0271a0001c0001t0004g0255a0002c0002t0003g0032others(2): Show | 5 | HG00738.hp2 HG01978.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.333-19318_333-1931 others(10): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64556417 | |||||
| chr5:64556417
|
C | CCCCA | 3 | a0001c0001t0001g0100a0001c0001t0011g0014a0002c0002t0001g0157 | 3 | HG01978.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.333-19356_333-1935 others(8): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64556417 | |||||
| chr5:64556417
|
CCA | C | 82 | a0001c0001t0001g0047a0001c0001t0001g0052a0001c0001t0001g0057others(79): Show | 83 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.333-19314_333-1931 others(6): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64556417 | |||||
| chr5:64556417
|
CCACA | C | 8 | a0001c0001t0001g0053a0001c0001t0002g0151a0001c0001t0002g0230others(5): Show | 8 | HG01361.hp1 HG01952.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.333-19316_333-1931 others(8): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64556417 | |||||
| chr5:64556417
|
CCACACA | C | 18 | a0001c0001t0001g0097a0001c0001t0001g0122a0001c0001t0001g0148others(15): Show | 20 | HG01106.hp2 HG01175.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.333-19318_333-1931 others(10): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64556417 | |||||
| chr5:64556417
|
CCACACAC others(7): Show |
C | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.333-19326_333-1931 others(18): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64556417 | |||||
| chr5:64556417
|
CCACACAC others(11): Show |
C | 5 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0076others(2): Show | 7 | HG02647.hp2 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.333-19330_333-1931 others(22): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64556417 | |||||
| chr5:64556435
|
A | ACACC | 5 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0088others(2): Show | 6 | HG02258.hp1 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.333-19336_333-1933 others(8): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64556435 | |||||
| chr5:64556444
|
CACACACA others(10): Show |
C | 1 | a0001c0001t0001g0078 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.333-19328_333-1931 others(21): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64556444 | |||||
| chr5:64556461
|
A | AC | 4 | a0001c0001t0007g0039a0001c0001t0010g0019a0002c0002t0003g0050others(1): Show | 4 | HG00423.hp2 HG00642.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.333-19313_333-1931 others(5): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64556461 | ||||||
| chr5:64556486
|
G | A | 1 | a0001c0001t0002g0198 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.333-19288G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64556486 | ||||||
| chr5:64556493
|
A | G | 1 | a0002c0002t0001g0157 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.333-19281A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64556493 | ||||||
| chr5:64556684
|
A | T | 7 | a0001c0001t0001g0100a0001c0001t0006g0087a0001c0001t0011g0014others(4): Show | 7 | HG01978.hp1 HG02257.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.333-19090A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64556684 | ||||||
| chr5:64556707
|
G | T | 5 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0088others(2): Show | 6 | HG02258.hp1 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.333-19067G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64556707 | ||||||
| chr5:64556943
|
C | T | 3 | a0001c0001t0013g0008a0001c0001t0013g0009a0001c0001t0021g0010 | 3 | HG02647.hp1 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.333-18831C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64556943 | ||||||
| chr5:64556980
|
C | T | 5 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0088others(2): Show | 6 | HG02258.hp1 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.333-18794C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64556980 | ||||||
| chr5:64557054
|
A | C | 1 | a0001c0001t0001g0259 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.333-18720A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64557054 | ||||||
| chr5:64557174
|
A | G | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG01256.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.333-18600A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64557174 | ||||||
| chr5:64557574
|
T | C | 61 | a0001c0001t0001g0214a0001c0001t0001g0269a0001c0001t0002g0006others(58): Show | 61 | HG00597.hp2 HG00738.hp2 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.333-18200T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64557574 | ||||||
| chr5:64557611
|
G | A | 5 | a0001c0001t0001g0074a0001c0001t0001g0174a0001c0001t0002g0240others(2): Show | 5 | HG01109.hp1 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.333-18163G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64557611 | ||||||
| chr5:64557651
|
A | G | 1 | a0001c0001t0002g0198 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.333-18123A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64557651 | ||||||
| chr5:64557714
|
A | G | 1 | a0001c0001t0002g0165 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.333-18060A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64557714 | ||||||
| chr5:64557793
|
T | C | 1 | a0002c0002t0001g0092 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.333-17981T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64557793 | ||||||
| chr5:64557802
|
T | C | 1 | a0002c0002t0001g0185 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.333-17972T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64557802 | ||||||
| chr5:64557891
|
C | G | 1 | a0001c0001t0013g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.333-17883C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64557891 | ||||||
| chr5:64557928
|
A | C | 1 | a0001c0001t0002g0211 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.333-17846A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64557928 | ||||||
| chr5:64558192
|
T | TGTG | 21 | a0001c0001t0001g0035a0001c0001t0001g0074a0001c0001t0001g0100others(18): Show | 22 | HG01109.hp1 HG01891.hp2 HG01978.hp1 others(19): Show |
intron_variant | MODIFIER | c.333-17582_333-1758 others(7): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64558192 | ||||||
| chr5:64558274
|
G | A | 2 | a0001c0001t0004g0083a0001c0001t0011g0014 | 2 | HG00639.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.333-17500G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64558274 | ||||||
| chr5:64558366
|
A | T | 1 | a0001c0001t0001g0174 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.333-17408A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64558366 | ||||||
| chr5:64558420
|
T | C | 61 | a0001c0001t0001g0214a0001c0001t0001g0269a0001c0001t0002g0006others(58): Show | 61 | HG00597.hp2 HG00738.hp2 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.333-17354T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64558420 | ||||||
| chr5:64558495
|
G | A | 1 | a0001c0001t0015g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.333-17279G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64558495 | ||||||
| chr5:64558586
|
A | C | 13 | a0001c0001t0001g0178a0001c0001t0001g0188a0001c0001t0001g0189others(10): Show | 13 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.333-17188A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64558586 | ||||||
| chr5:64558623
|
A | G | 10 | a0001c0001t0001g0074a0001c0001t0001g0174a0001c0001t0002g0002others(7): Show | 11 | HG01109.hp1 HG01891.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.333-17151A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64558623 | ||||||
| chr5:64558852
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.333-16922C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64558852 | ||||||
| chr5:64558888
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.333-16886C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64558888 | ||||||
| chr5:64558982
|
T | A | 5 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0088others(2): Show | 6 | HG02258.hp1 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.333-16792T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64558982 | ||||||
| chr5:64558991
|
G | A | 1 | a0001c0001t0015g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.333-16783G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64558991 | ||||||
| chr5:64559000
|
G | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0047others(87): Show | 95 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.333-16774G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64559000 | ||||||
| chr5:64559074
|
C | T | 5 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0088others(2): Show | 6 | HG02258.hp1 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.333-16700C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64559074 | ||||||
| chr5:64559142
|
A | G | 61 | a0001c0001t0001g0214a0001c0001t0001g0269a0001c0001t0002g0006others(58): Show | 61 | HG00597.hp2 HG00738.hp2 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.333-16632A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64559142 | ||||||
| chr5:64559153
|
T | C | 20 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0030others(17): Show | 20 | HG00099.hp2 HG00423.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.333-16621T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64559153 | ||||||
| chr5:64559189
|
A | C | 5 | a0001c0001t0001g0074a0001c0001t0001g0174a0001c0001t0002g0240others(2): Show | 5 | HG01109.hp1 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.333-16585A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64559189 | ||||||
| chr5:64559275
|
G | A | 1 | a0001c0001t0004g0223 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.333-16499G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64559275 | ||||||
| chr5:64559372
|
G | A | 1 | a0001c0001t0021g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.333-16402G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64559372 | ||||||
| chr5:64559531
|
A | G | 1 | a0001c0001t0008g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.333-16243A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64559531 | ||||||
| chr5:64559562
|
A | G | 3 | a0001c0001t0013g0008a0001c0001t0013g0009a0001c0001t0021g0010 | 3 | HG02647.hp1 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.333-16212A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64559562 | ||||||
| chr5:64559647
|
G | A | 1 | a0002c0002t0003g0031 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.333-16127G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64559647 | ||||||
| chr5:64559733
|
G | A | 5 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0088others(2): Show | 6 | HG02258.hp1 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.333-16041G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64559733 | ||||||
| chr5:64559827
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.333-15947T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64559827 | ||||||
| chr5:64559836
|
C | G | 11 | a0001c0001t0004g0267a0002c0002t0001g0004a0002c0002t0001g0005others(8): Show | 13 | HG01106.hp2 HG01433.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.333-15938C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64559836 | ||||||
| chr5:64559873
|
C | A | 60 | a0001c0001t0001g0214a0001c0001t0001g0269a0001c0001t0002g0006others(57): Show | 60 | HG00597.hp2 HG00738.hp2 HG01074.hp1 others(57): Show |
intron_variant | MODIFIER | c.333-15901C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64559873 | ||||||
| chr5:64559879
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.333-15895C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64559879 | ||||||
| chr5:64560014
|
T | C | 1 | a0001c0001t0004g0223 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.333-15760T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64560014 | ||||||
| chr5:64560095
|
G | A | 5 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0004g0015others(2): Show | 5 | HG02451.hp2 HG02895.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.333-15679G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64560095 | ||||||
| chr5:64560163
|
A | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0174a0001c0001t0008g0007 | 3 | HG01891.hp2 HG02486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.333-15611A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64560163 | ||||||
| chr5:64560283
|
C | T | 233 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0021others(230): Show | 239 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.333-15491C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64560283 | ||||||
| chr5:64560482
|
G | A | 40 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0030others(37): Show | 40 | HG00099.hp2 HG00423.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.333-15292G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64560482 | ||||||
| chr5:64560493
|
C | T | 1 | a0001c0001t0002g0240 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.333-15281C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64560493 | ||||||
| chr5:64560543
|
G | GTA | 56 | a0001c0001t0001g0214a0001c0001t0001g0269a0001c0001t0002g0006others(53): Show | 56 | HG00597.hp2 HG00738.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.333-15212_333-1521 others(6): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64560543 | |||||
| chr5:64560543
|
G | GTATA | 17 | a0001c0001t0001g0174a0001c0001t0001g0177a0001c0001t0002g0208others(14): Show | 17 | HG01167.hp1 HG01884.hp1 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.333-15214_333-1521 others(8): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64560543 | |||||
| chr5:64560543
|
G | GTATATA | 4 | a0001c0001t0001g0074a0001c0001t0002g0240a0001c0001t0008g0007others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.333-15216_333-1521 others(10): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64560543 | |||||
| chr5:64560543
|
GTA | G | 64 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0023others(61): Show | 64 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.333-15212_333-1521 others(6): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64560543 | |||||
| chr5:64560543
|
GTATA | G | 9 | a0001c0001t0001g0035a0001c0001t0001g0100a0001c0001t0004g0041others(6): Show | 9 | HG01978.hp1 HG02145.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.333-15214_333-1521 others(8): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64560543 | |||||
| chr5:64560582
|
AT | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0030a0002c0002t0001g0159others(1): Show | 4 | NA18941.hp2 NA18977.hp2 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.333-15190delT | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64560582 | |||||
| chr5:64560627
|
C | T | 12 | a0001c0001t0001g0035a0001c0001t0001g0100a0001c0001t0004g0041others(9): Show | 12 | HG01978.hp1 HG02145.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.333-15147C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64560627 | ||||||
| chr5:64560722
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.333-15052C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64560722 | ||||||
| chr5:64560742
|
C | G | 1 | a0001c0001t0001g0122 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.333-15032C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64560742 | ||||||
| chr5:64560917
|
C | T | 2 | a0001c0001t0001g0194a0001c0001t0001g0237 | 2 | HG02055.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.333-14857C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64560917 | ||||||
| chr5:64560953
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.333-14821T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64560953 | ||||||
| chr5:64560963
|
A | G | 2 | a0001c0001t0002g0044a0001c0001t0009g0054 | 2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.333-14811A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64560963 | ||||||
| chr5:64560981
|
G | A | 61 | a0001c0001t0001g0214a0001c0001t0001g0269a0001c0001t0002g0006others(58): Show | 61 | HG00597.hp2 HG00738.hp2 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.333-14793G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64560981 | ||||||
| chr5:64561051
|
C | T | 2 | a0002c0002t0001g0228a0002c0002t0001g0229 | 2 | HG02257.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.333-14723C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64561051 | ||||||
| chr5:64561056
|
C | T | 4 | a0001c0001t0001g0053a0001c0001t0001g0058a0001c0001t0001g0067others(1): Show | 4 | HG02145.hp1 HG02572.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.333-14718C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64561056 | ||||||
| chr5:64561057
|
G | A | 1 | a0001c0001t0004g0037 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.333-14717G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64561057 | ||||||
| chr5:64561102
|
C | G | 3 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0006g0187 | 3 | HG03139.hp2 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.333-14672C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64561102 | ||||||
| chr5:64561137
|
C | T | 1 | a0002c0002t0001g0264 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.333-14637C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64561137 | ||||||
| chr5:64561423
|
G | A | 212 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0029others(209): Show | 218 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.333-14351G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64561423 | ||||||
| chr5:64561812
|
C | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0174a0001c0001t0008g0007 | 3 | HG01891.hp2 HG02486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.333-13962C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64561812 | ||||||
| chr5:64561861
|
A | AGCTATTT others(267): Show |
2 | a0001c0001t0002g0002a0001c0001t0002g0018 | 3 | HG03098.hp2 HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.333-13898_333-1389 others(278): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64561861 | |||||
| chr5:64561861
|
A | AGCTATTT others(268): Show |
3 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0006g0086 | 3 | HG02258.hp1 HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.333-13898_333-1389 others(279): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64561861 | |||||
| chr5:64561984
|
G | A | 3 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0006g0187 | 3 | HG03139.hp2 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.333-13790G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64561984 | ||||||
| chr5:64562071
|
A | C | 1 | a0002c0002t0003g0112 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.333-13703A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64562071 | ||||||
| chr5:64562126
|
G | A | 173 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0040others(170): Show | 179 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(176): Show |
intron_variant | MODIFIER | c.333-13648G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64562126 | ||||||
| chr5:64562452
|
G | A | 2 | a0002c0002t0001g0228a0002c0002t0001g0229 | 2 | HG02257.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.333-13322G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64562452 | ||||||
| chr5:64562536
|
C | T | 1 | a0002c0002t0006g0085 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.333-13238C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64562536 | ||||||
| chr5:64562559
|
G | A | 2 | a0001c0001t0002g0151a0001c0001t0002g0230 | 2 | HG01361.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.333-13215G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64562559 | ||||||
| chr5:64562579
|
T | C | 2 | a0001c0001t0001g0046a0001c0001t0001g0109 | 2 | HG00741.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.333-13195T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64562579 | ||||||
| chr5:64562678
|
C | G | 1 | a0001c0001t0008g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.333-13096C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64562678 | ||||||
| chr5:64563255
|
A | G | 60 | a0001c0001t0001g0214a0001c0001t0001g0269a0001c0001t0002g0006others(57): Show | 60 | HG00597.hp2 HG00738.hp2 HG01074.hp1 others(57): Show |
intron_variant | MODIFIER | c.333-12519A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64563255 | ||||||
| chr5:64563284
|
T | C | 1 | a0002c0002t0003g0199 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.333-12490T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64563284 | ||||||
| chr5:64563344
|
A | T | 5 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0088others(2): Show | 6 | HG02258.hp1 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.333-12430A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64563344 | ||||||
| chr5:64564044
|
T | C | 4 | a0001c0001t0001g0035a0001c0001t0004g0041a0001c0001t0004g0254others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.333-11730T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64564044 | ||||||
| chr5:64564055
|
G | A | 7 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0046others(4): Show | 7 | HG00741.hp2 HG03471.hp2 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.333-11719G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64564055 | ||||||
| chr5:64564063
|
C | G | 4 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0088others(1): Show | 5 | HG02258.hp1 HG03098.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.333-11711C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64564063 | ||||||
| chr5:64564076
|
A | G | 5 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0088others(2): Show | 6 | HG02258.hp1 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.333-11698A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64564076 | ||||||
| chr5:64564164
|
T | A | 1 | a0001c0001t0002g0209 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.333-11610T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64564164 | ||||||
| chr5:64564208
|
G | A | 5 | a0001c0001t0004g0022a0001c0001t0004g0158a0001c0001t0004g0167others(2): Show | 5 | HG00423.hp2 HG02015.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.333-11566G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64564208 | ||||||
| chr5:64564314
|
C | T | 212 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0029others(209): Show | 218 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.333-11460C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64564314 | ||||||
| chr5:64564483
|
T | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0047others(87): Show | 95 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.333-11291T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64564483 | ||||||
| chr5:64564510
|
C | T | 40 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0030others(37): Show | 40 | HG00099.hp2 HG00423.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.333-11264C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64564510 | ||||||
| chr5:64564814
|
G | C | 1 | a0001c0001t0001g0070 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.333-10960G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64564814 | ||||||
| chr5:64564898
|
C | A | 5 | a0001c0001t0001g0074a0001c0001t0001g0174a0001c0001t0002g0240others(2): Show | 5 | HG01109.hp1 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.333-10876C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64564898 | ||||||
| chr5:64565036
|
A | G | 1 | a0001c0001t0001g0052 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.333-10738A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64565036 | ||||||
| chr5:64565037
|
T | C | 1 | a0001c0001t0015g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.333-10737T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64565037 | ||||||
| chr5:64565140
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.333-10634G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64565140 | ||||||
| chr5:64565159
|
A | C | 5 | a0001c0001t0001g0100a0001c0001t0006g0087a0001c0001t0011g0013others(2): Show | 5 | HG01978.hp1 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.333-10615A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64565159 | ||||||
| chr5:64565275
|
A | C | 5 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0088others(2): Show | 6 | HG02258.hp1 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.333-10499A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64565275 | ||||||
| chr5:64565296
|
ATATAT | A | 5 | a0001c0001t0001g0074a0001c0001t0001g0174a0001c0001t0002g0240others(2): Show | 5 | HG01109.hp1 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.333-10472_333-1046 others(9): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64565296 | |||||
| chr5:64565335
|
C | A | 9 | a0001c0001t0001g0100a0001c0001t0001g0113a0001c0001t0002g0251others(6): Show | 9 | HG01978.hp1 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.333-10439C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64565335 | ||||||
| chr5:64565457
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.333-10317C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64565457 | ||||||
| chr5:64565461
|
G | C | 1 | a0001c0001t0002g0121 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.333-10313G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64565461 | ||||||
| chr5:64565516
|
T | A | 11 | a0001c0001t0001g0035a0001c0001t0002g0239a0001c0001t0004g0254others(8): Show | 12 | HG02145.hp2 HG02559.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.333-10258T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64565516 | ||||||
| chr5:64565516
|
T | TA | 6 | a0001c0001t0001g0074a0001c0001t0001g0174a0001c0001t0001g0269others(3): Show | 6 | HG01109.hp1 HG01891.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.333-10250dupA | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64565516 | |||||
| chr5:64565517
|
A | T | 1 | a0002c0002t0003g0163 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.333-10257A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64565517 | ||||||
| chr5:64565527
|
A | G | 5 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0088others(2): Show | 6 | HG02258.hp1 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.333-10247A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64565527 | ||||||
| chr5:64565546
|
C | T | 3 | a0001c0001t0013g0008a0001c0001t0013g0009a0001c0001t0021g0010 | 3 | HG02647.hp1 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.333-10228C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64565546 | ||||||
| chr5:64565554
|
A | T | 1 | a0001c0001t0006g0086 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.333-10220A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64565554 | ||||||
| chr5:64565606
|
C | T | 40 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0030others(37): Show | 40 | HG00099.hp2 HG00423.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.333-10168C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64565606 | ||||||
| chr5:64565648
|
A | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0029others(210): Show | 219 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(216): Show |
intron_variant | MODIFIER | c.333-10126A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64565648 | ||||||
| chr5:64565657
|
T | A | 104 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0030others(101): Show | 104 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.333-10117T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64565657 | ||||||
| chr5:64565668
|
T | C | 105 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0030others(102): Show | 105 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.333-10106T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64565668 | ||||||
| chr5:64565674
|
C | T | 1 | a0002c0002t0001g0012 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.333-10100C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64565674 | ||||||
| chr5:64565675
|
G | A | 2 | a0001c0001t0004g0254a0001c0001t0004g0255 | 2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.333-10099G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64565675 | ||||||
| chr5:64565870
|
T | C | 1 | a0001c0001t0004g0139 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.333-9904T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64565870 | ||||||
| chr5:64566047
|
G | T | 1 | a0002c0002t0003g0207 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.333-9727G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64566047 | ||||||
| chr5:64566177
|
G | GTATGATA others(24): Show |
2 | a0001c0001t0004g0015a0001c0001t0004g0036 | 2 | HG02451.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.333-9595_333-9565d others(33): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64566177 | |||||
| chr5:64566325
|
A | C | 6 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0088others(3): Show | 7 | HG02258.hp1 HG02717.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.333-9449A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64566325 | ||||||
| chr5:64566371
|
T | G | 1 | a0001c0001t0011g0013 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.333-9403T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64566371 | ||||||
| chr5:64566605
|
C | T | 5 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0088others(2): Show | 6 | HG02258.hp1 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.333-9169C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64566605 | ||||||
| chr5:64566675
|
A | G | 1 | a0001c0001t0008g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.333-9099A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64566675 | ||||||
| chr5:64566676
|
C | T | 4 | a0001c0001t0005g0116a0001c0001t0005g0190a0001c0001t0005g0272others(1): Show | 4 | NA18951.hp1 NA18986.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.333-9098C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64566676 | ||||||
| chr5:64566686
|
G | T | 1 | a0001c0001t0008g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.333-9088G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64566686 | ||||||
| chr5:64567086
|
G | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0034others(205): Show | 214 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(211): Show |
intron_variant | MODIFIER | c.333-8688G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64567086 | ||||||
| chr5:64567124
|
C | T | 1 | a0001c0001t0002g0217 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.333-8650C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64567124 | ||||||
| chr5:64567126
|
C | T | 1 | a0001c0001t0002g0217 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.333-8648C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64567126 | ||||||
| chr5:64567131
|
A | G | 1 | a0001c0001t0002g0217 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.333-8643A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64567131 | ||||||
| chr5:64567135
|
C | T | 1 | a0001c0001t0002g0217 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.333-8639C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64567135 | ||||||
| chr5:64567151
|
G | T | 1 | a0002c0002t0003g0156 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.333-8623G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64567151 | ||||||
| chr5:64567337
|
T | C | 1 | a0001c0001t0004g0223 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.333-8437T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64567337 | ||||||
| chr5:64567359
|
TTAAAA | T | 2 | a0001c0001t0001g0100a0002c0002t0001g0157 | 2 | HG01978.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.333-8412_333-8408d others(7): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64567359 | |||||
| chr5:64567364
|
A | G | 215 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0029others(212): Show | 221 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.333-8410A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64567364 | ||||||
| chr5:64567406
|
T | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0052others(92): Show | 98 | HG00597.hp2 HG00639.hp1 HG00738.hp2 others(95): Show |
intron_variant | MODIFIER | c.333-8368T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64567406 | ||||||
| chr5:64567452
|
C | T | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG01256.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.333-8322C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64567452 | ||||||
| chr5:64567526
|
C | T | 3 | a0001c0001t0004g0254a0001c0001t0004g0255a0001c0001t0011g0013 | 3 | HG02451.hp1 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.333-8248C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64567526 | ||||||
| chr5:64567589
|
G | T | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.333-8185G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64567589 | ||||||
| chr5:64567706
|
T | TA | 25 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0055others(22): Show | 26 | HG00099.hp1 HG00642.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.333-8067dupA | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64567706 | |||||
| chr5:64567755
|
T | C | 1 | a0001c0001t0006g0086 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.333-8019T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64567755 | ||||||
| chr5:64567795
|
A | G | 83 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0075others(80): Show | 86 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.333-7979A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64567795 | ||||||
| chr5:64567852
|
C | T | 26 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0046others(23): Show | 28 | HG00099.hp2 HG00741.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.333-7922C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64567852 | ||||||
| chr5:64567856
|
A | G | 3 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0006g0187 | 3 | HG03139.hp2 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.333-7918A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64567856 | ||||||
| chr5:64567879
|
T | TTTATATA others(11): Show |
4 | a0002c0002t0001g0004a0002c0002t0001g0228a0002c0002t0001g0229others(1): Show | 5 | HG01106.hp2 HG02257.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.333-7894_333-7893i others(20): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64567879 | |||||
| chr5:64567881
|
C | A | 4 | a0002c0002t0001g0004a0002c0002t0001g0228a0002c0002t0001g0229others(1): Show | 5 | HG01106.hp2 HG02257.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.333-7893C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64567881 | ||||||
| chr5:64567883
|
T | A | 4 | a0002c0002t0001g0004a0002c0002t0001g0228a0002c0002t0001g0229others(1): Show | 5 | HG01106.hp2 HG02257.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.333-7891T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64567883 | ||||||
| chr5:64568074
|
T | C | 1 | a0001c0001t0004g0223 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.333-7700T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64568074 | ||||||
| chr5:64568257
|
C | T | 3 | a0001c0001t0004g0223a0001c0001t0013g0008a0001c0001t0013g0009 | 3 | HG01257.hp1 HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.333-7517C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64568257 | ||||||
| chr5:64568268
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.333-7506C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64568268 | ||||||
| chr5:64568570
|
G | A | 18 | a0001c0001t0001g0040a0001c0001t0001g0055a0001c0001t0001g0060others(15): Show | 19 | HG00099.hp1 HG00642.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.333-7204G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64568570 | ||||||
| chr5:64568674
|
A | G | 118 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0034others(115): Show | 121 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.333-7100A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64568674 | ||||||
| chr5:64568694
|
A | C | 2 | a0001c0001t0002g0173a0001c0001t0002g0175 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.333-7080A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64568694 | ||||||
| chr5:64568782
|
G | GA | 70 | a0001c0001t0001g0021a0001c0001t0001g0214a0001c0001t0001g0269others(67): Show | 71 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.333-6992_333-6991i others(3): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64568782 | ||||||
| chr5:64568782
|
G | GT | 51 | a0001c0001t0001g0047a0001c0001t0001g0053a0001c0001t0001g0057others(48): Show | 51 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.333-6977dupT | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64568782 | |||||
| chr5:64568782
|
GT | G | 6 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0005g0116others(3): Show | 6 | HG01978.hp1 HG02257.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.333-6977delT | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64568782 | |||||
| chr5:64568783
|
T | A | 25 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0055others(22): Show | 26 | HG00099.hp1 HG00642.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.333-6991T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64568783 | ||||||
| chr5:64568784
|
T | A | 5 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0006g0087others(2): Show | 5 | HG01978.hp1 HG02257.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.333-6990T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64568784 | ||||||
| chr5:64568795
|
T | C | 23 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0046others(20): Show | 25 | HG00099.hp2 HG00741.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.333-6979T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64568795 | ||||||
| chr5:64568852
|
A | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0029others(195): Show | 204 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(201): Show |
intron_variant | MODIFIER | c.333-6922A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64568852 | ||||||
| chr5:64568908
|
G | A | 3 | a0001c0001t0004g0015a0001c0001t0004g0036a0001c0001t0004g0037 | 3 | HG02451.hp2 HG02572.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.333-6866G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64568908 | ||||||
| chr5:64568938
|
CA | C | 104 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0030others(101): Show | 107 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(104): Show |
intron_variant | MODIFIER | c.333-6834delA | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64568938 | |||||
| chr5:64568959
|
C | T | 5 | a0002c0002t0001g0004a0002c0002t0001g0228a0002c0002t0001g0229others(2): Show | 6 | HG01106.hp2 HG02257.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.333-6815C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64568959 | ||||||
| chr5:64569065
|
C | T | 6 | a0001c0001t0004g0223a0001c0001t0004g0254a0001c0001t0004g0255others(3): Show | 6 | HG01257.hp1 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.333-6709C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64569065 | ||||||
| chr5:64569090
|
T | C | 1 | a0001c0001t0004g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.333-6684T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64569090 | ||||||
| chr5:64569219
|
A | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0029others(199): Show | 208 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(205): Show |
intron_variant | MODIFIER | c.333-6555A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64569219 | ||||||
| chr5:64569225
|
G | A | 1 | a0001c0001t0015g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.333-6549G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64569225 | ||||||
| chr5:64569291
|
C | CA | 18 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0075others(15): Show | 20 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.333-6474dupA | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64569291 | |||||
| chr5:64569460
|
T | C | 1 | a0001c0001t0001g0052 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.333-6314T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64569460 | ||||||
| chr5:64569628
|
A | G | 6 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0006g0086others(3): Show | 6 | HG01978.hp1 HG02257.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.333-6146A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64569628 | ||||||
| chr5:64569677
|
A | T | 25 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0055others(22): Show | 26 | HG00099.hp1 HG00642.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.333-6097A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64569677 | ||||||
| chr5:64569692
|
A | T | 211 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0029others(208): Show | 217 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.333-6082A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64569692 | ||||||
| chr5:64569694
|
T | C | 1 | a0001c0001t0002g0213 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.333-6080T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64569694 | ||||||
| chr5:64569704
|
A | C | 16 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0076others(13): Show | 18 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.333-6070A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64569704 | ||||||
| chr5:64569770
|
C | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0029others(205): Show | 214 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(211): Show |
intron_variant | MODIFIER | c.333-6004C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64569770 | ||||||
| chr5:64569905
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.333-5869C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64569905 | ||||||
| chr5:64570077
|
C | T | 4 | a0001c0001t0015g0017a0002c0002t0001g0012a0002c0002t0001g0095others(1): Show | 4 | HG01884.hp1 HG03041.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.333-5697C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64570077 | ||||||
| chr5:64570203
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.333-5571C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64570203 | ||||||
| chr5:64570295
|
C | T | 3 | a0001c0001t0004g0015a0001c0001t0004g0036a0001c0001t0004g0037 | 3 | HG02451.hp2 HG02572.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.333-5479C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64570295 | ||||||
| chr5:64570503
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0010g0019 | 2 | HG00642.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.333-5271C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64570503 | ||||||
| chr5:64570632
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.333-5142G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64570632 | ||||||
| chr5:64570794
|
C | T | 1 | a0001c0001t0008g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.333-4980C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64570794 | ||||||
| chr5:64570865
|
A | T | 5 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0006g0087others(2): Show | 5 | HG01978.hp1 HG02257.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.333-4909A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64570865 | ||||||
| chr5:64571026
|
G | A | 1 | a0001c0001t0004g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.333-4748G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64571026 | ||||||
| chr5:64571046
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.333-4728A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64571046 | ||||||
| chr5:64571242
|
TG | T | 3 | a0001c0001t0004g0254a0001c0001t0004g0255a0001c0001t0011g0013 | 3 | HG02451.hp1 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.333-4531delG | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64571242 | ||||||
| chr5:64571723
|
C | A | 160 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0030others(157): Show | 163 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(160): Show |
intron_variant | MODIFIER | c.333-4051C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64571723 | ||||||
| chr5:64571783
|
T | C | 1 | a0001c0001t0011g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.333-3991T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64571783 | ||||||
| chr5:64571987
|
G | A | 2 | a0002c0002t0003g0170a0002c0002t0003g0171 | 2 | NA18939.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.333-3787G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64571987 | ||||||
| chr5:64572148
|
A | T | 25 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0055others(22): Show | 26 | HG00099.hp1 HG00642.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.333-3626A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64572148 | ||||||
| chr5:64572237
|
T | C | 1 | a0001c0001t0006g0086 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.333-3537T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64572237 | ||||||
| chr5:64572266
|
T | C | 1 | a0001c0001t0002g0217 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.333-3508T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64572266 | ||||||
| chr5:64572376
|
C | T | 2 | a0001c0001t0013g0008a0001c0001t0013g0009 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.333-3398C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64572376 | ||||||
| chr5:64572441
|
A | G | 188 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0030others(185): Show | 192 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.333-3333A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64572441 | ||||||
| chr5:64572499
|
T | C | 9 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0076others(6): Show | 11 | HG02109.hp1 HG02615.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.333-3275T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64572499 | ||||||
| chr5:64572530
|
T | A | 1 | a0001c0001t0006g0087 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.333-3244T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64572530 | ||||||
| chr5:64572559
|
A | G | 8 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0043others(5): Show | 9 | HG02258.hp1 HG02965.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.333-3215A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64572559 | ||||||
| chr5:64572627
|
T | G | 3 | a0001c0001t0002g0006a0001c0001t0002g0121a0001c0001t0002g0219 | 3 | HG00639.hp1 HG01168.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.333-3147T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64572627 | ||||||
| chr5:64572807
|
C | CT | 24 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0055others(21): Show | 25 | HG00099.hp1 HG00642.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.333-2956dupT | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64572807 | |||||
| chr5:64572967
|
C | T | 1 | a0002c0002t0001g0012 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.333-2807C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64572967 | ||||||
| chr5:64572975
|
C | A | 1 | a0001c0001t0001g0109 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.333-2799C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64572975 | ||||||
| chr5:64573065
|
G | A | 1 | a0001c0001t0008g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.333-2709G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64573065 | ||||||
| chr5:64573138
|
G | C | 1 | a0001c0001t0004g0016 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.333-2636G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64573138 | ||||||
| chr5:64573166
|
T | G | 193 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0030others(190): Show | 197 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(194): Show |
intron_variant | MODIFIER | c.333-2608T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64573166 | ||||||
| chr5:64573184
|
T | C | 25 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0055others(22): Show | 26 | HG00099.hp1 HG00642.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.333-2590T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64573184 | ||||||
| chr5:64573476
|
G | C | 1 | a0001c0001t0001g0214 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.333-2298G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64573476 | ||||||
| chr5:64573547
|
T | A | 3 | a0002c0002t0003g0032a0002c0002t0003g0033a0002c0002t0003g0162 | 3 | HG00738.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.333-2227T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64573547 | ||||||
| chr5:64573547
|
T | TA | 37 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0040others(34): Show | 40 | HG00099.hp1 HG00642.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.333-2217dupA | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64573547 | |||||
| chr5:64573547
|
TA | T | 5 | a0001c0001t0015g0017a0002c0002t0001g0012a0002c0002t0001g0095others(2): Show | 5 | HG01884.hp1 HG03041.hp1 NA19065.hp2 others(2): Show |
intron_variant | MODIFIER | c.333-2217delA | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 64573547 | |||||
| chr5:64573657
|
C | A | 1 | a0001c0001t0008g0007 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.333-2117C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64573657 | ||||||
| chr5:64573776
|
T | C | 1 | a0001c0001t0006g0086 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.333-1998T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64573776 | ||||||
| chr5:64573951
|
T | A | 1 | a0001c0001t0002g0263 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.333-1823T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64573951 | ||||||
| chr5:64573959
|
A | T | 68 | a0001c0001t0001g0021a0001c0001t0001g0214a0001c0001t0001g0269others(65): Show | 69 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.333-1815A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64573959 | ||||||
| chr5:64574135
|
A | G | 5 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0006g0087others(2): Show | 5 | HG01978.hp1 HG02257.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.333-1639A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64574135 | ||||||
| chr5:64574191
|
A | G | 5 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0006g0087others(2): Show | 5 | HG01978.hp1 HG02257.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.333-1583A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64574191 | ||||||
| chr5:64574250
|
G | A | 1 | a0001c0001t0011g0013 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.333-1524G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64574250 | ||||||
| chr5:64574409
|
C | T | 1 | a0001c0001t0006g0086 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.333-1365C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64574409 | ||||||
| chr5:64574659
|
G | A | 1 | a0002c0002t0001g0264 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.333-1115G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64574659 | ||||||
| chr5:64574840
|
A | G | 5 | a0001c0001t0015g0017a0002c0002t0001g0012a0002c0002t0001g0095others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.333-934A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64574840 | ||||||
| chr5:64575128
|
A | G | 5 | a0001c0001t0002g0208a0001c0001t0002g0212a0001c0001t0002g0218others(2): Show | 5 | HG01934.hp2 HG01952.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.333-646A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64575128 | ||||||
| chr5:64575282
|
A | C | 1 | a0002c0002t0001g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.333-492A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64575282 | ||||||
| chr5:64575283
|
T | C | 188 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0030others(185): Show | 192 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.333-491T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64575283 | ||||||
| chr5:64575346
|
T | C | 15 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0076others(12): Show | 17 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.333-428T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64575346 | ||||||
| chr5:64575544
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0002c0002t0001g0159 | 3 | NA18977.hp2 NA19084.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.333-230G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 2/5 | chr5 | 64575544 | ||||||
| chr5:64576250
|
A | G | 2 | a0002c0002t0003g0170a0002c0002t0003g0171 | 2 | NA18939.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.463+346A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64576250 | ||||||
| chr5:64576523
|
C | T | 1 | a0001c0001t0011g0013 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.463+619C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64576523 | ||||||
| chr5:64576571
|
G | C | 1 | a0002c0002t0003g0119 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.463+667G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64576571 | ||||||
| chr5:64576605
|
A | T | 2 | a0001c0001t0013g0008a0001c0001t0013g0009 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.463+701A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64576605 | ||||||
| chr5:64576607
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0020g0101 | 2 | HG00741.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.463+703C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64576607 | ||||||
| chr5:64576628
|
C | T | 273 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0021others(270): Show | 279 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.463+724C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64576628 | ||||||
| chr5:64576798
|
G | T | 1 | a0002c0002t0001g0091 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.463+894G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64576798 | ||||||
| chr5:64576879
|
G | T | 1 | a0001c0001t0001g0120 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.463+975G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64576879 | ||||||
| chr5:64577057
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.463+1153T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64577057 | ||||||
| chr5:64577084
|
TA | T | 211 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0029others(208): Show | 217 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.463+1185delA | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 64577084 | |||||
| chr5:64577135
|
G | A | 46 | a0001c0001t0001g0047a0001c0001t0001g0053a0001c0001t0001g0057others(43): Show | 46 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.463+1231G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64577135 | ||||||
| chr5:64577165
|
A | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0029others(207): Show | 216 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.463+1261A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64577165 | ||||||
| chr5:64577210
|
G | A | 5 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0006g0187others(2): Show | 5 | HG01109.hp1 HG03098.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.463+1306G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64577210 | ||||||
| chr5:64577221
|
G | A | 1 | a0002c0002t0001g0185 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.463+1317G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64577221 | ||||||
| chr5:64577308
|
G | C | 75 | a0001c0001t0001g0021a0001c0001t0001g0059a0001c0001t0001g0214others(72): Show | 76 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.463+1404G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64577308 | ||||||
| chr5:64577350
|
G | C | 2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.463+1446G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64577350 | ||||||
| chr5:64577357
|
G | C | 1 | a0002c0002t0001g0266 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.463+1453G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64577357 | ||||||
| chr5:64577456
|
A | G | 1 | a0002c0002t0003g0163 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.463+1552A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64577456 | ||||||
| chr5:64577468
|
C | T | 1 | a0001c0001t0020g0101 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.463+1564C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64577468 | ||||||
| chr5:64577503
|
A | G | 3 | a0001c0001t0001g0177a0002c0002t0001g0180a0002c0002t0001g0181 | 3 | HG02809.hp2 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.463+1599A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64577503 | ||||||
| chr5:64577659
|
G | C | 1 | a0001c0001t0001g0035 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.463+1755G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64577659 | ||||||
| chr5:64577734
|
C | G | 3 | a0001c0001t0001g0100a0001c0001t0011g0014a0002c0002t0001g0157 | 3 | HG01978.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.463+1830C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64577734 | ||||||
| chr5:64577814
|
A | G | 8 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0043others(5): Show | 9 | HG02258.hp1 HG02965.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.463+1910A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64577814 | ||||||
| chr5:64577950
|
T | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0029others(209): Show | 218 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(215): Show |
intron_variant | MODIFIER | c.463+2046T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64577950 | ||||||
| chr5:64578308
|
A | G | 3 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0006g0187 | 3 | HG03139.hp2 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.463+2404A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64578308 | ||||||
| chr5:64578581
|
A | G | 2 | a0002c0002t0003g0170a0002c0002t0003g0171 | 2 | NA18939.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.463+2677A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64578581 | ||||||
| chr5:64578697
|
C | T | 1 | a0002c0002t0003g0042 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.463+2793C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64578697 | ||||||
| chr5:64578790
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.463+2886G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64578790 | ||||||
| chr5:64578799
|
A | G | 62 | a0001c0001t0001g0021a0001c0001t0001g0059a0001c0001t0001g0214others(59): Show | 62 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.463+2895A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64578799 | ||||||
| chr5:64578970
|
T | C | 16 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0076others(13): Show | 18 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.463+3066T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64578970 | ||||||
| chr5:64579036
|
A | G | 62 | a0001c0001t0001g0021a0001c0001t0001g0059a0001c0001t0001g0214others(59): Show | 62 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.463+3132A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64579036 | ||||||
| chr5:64579092
|
T | G | 23 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0046others(20): Show | 25 | HG00099.hp2 HG00741.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.463+3188T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64579092 | ||||||
| chr5:64579142
|
T | C | 5 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0006g0087others(2): Show | 5 | HG01978.hp1 HG02257.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.463+3238T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64579142 | ||||||
| chr5:64579193
|
T | C | 1 | a0001c0001t0006g0086 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.463+3289T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64579193 | ||||||
| chr5:64579215
|
G | T | 212 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0029others(209): Show | 218 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(215): Show |
intron_variant | MODIFIER | c.463+3311G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64579215 | ||||||
| chr5:64579275
|
A | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0029others(211): Show | 220 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(217): Show |
intron_variant | MODIFIER | c.463+3371A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64579275 | ||||||
| chr5:64579320
|
C | T | 4 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0006g0086others(1): Show | 4 | HG02717.hp2 HG03139.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+3416C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64579320 | ||||||
| chr5:64579405
|
G | T | 46 | a0001c0001t0001g0047a0001c0001t0001g0053a0001c0001t0001g0057others(43): Show | 46 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.463+3501G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64579405 | ||||||
| chr5:64579543
|
C | CA | 6 | a0001c0001t0001g0024a0001c0001t0001g0177a0001c0001t0005g0116others(3): Show | 6 | HG01175.hp1 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.463+3664dupA | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 64579543 | |||||
| chr5:64579543
|
CA | C | 175 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0029others(172): Show | 178 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(175): Show |
intron_variant | MODIFIER | c.463+3664delA | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 64579543 | |||||
| chr5:64579543
|
CAA | C | 32 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0076others(29): Show | 35 | HG01168.hp1 HG01256.hp1 HG01433.hp2 others(32): Show |
intron_variant | MODIFIER | c.463+3663_463+3664d others(4): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 64579543 | |||||
| chr5:64579570
|
G | A | 2 | a0001c0001t0013g0008a0001c0001t0013g0009 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.463+3666G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64579570 | ||||||
| chr5:64579660
|
C | T | 1 | a0002c0002t0006g0085 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.463+3756C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64579660 | ||||||
| chr5:64579866
|
T | C | 2 | a0001c0001t0013g0008a0001c0001t0013g0009 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.463+3962T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64579866 | ||||||
| chr5:64579983
|
A | T | 187 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0029others(184): Show | 192 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(189): Show |
intron_variant | MODIFIER | c.463+4079A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64579983 | ||||||
| chr5:64579994
|
C | T | 212 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0029others(209): Show | 218 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(215): Show |
intron_variant | MODIFIER | c.463+4090C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64579994 | ||||||
| chr5:64580136
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.463+4232T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64580136 | ||||||
| chr5:64580160
|
A | T | 2 | a0001c0001t0013g0008a0001c0001t0013g0009 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.463+4256A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64580160 | ||||||
| chr5:64580248
|
A | G | 1 | a0001c0001t0011g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.463+4344A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64580248 | ||||||
| chr5:64580308
|
A | G | 1 | a0001c0001t0011g0013 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.463+4404A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64580308 | ||||||
| chr5:64580310
|
C | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0029others(186): Show | 195 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(192): Show |
intron_variant | MODIFIER | c.463+4406C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64580310 | ||||||
| chr5:64580571
|
T | C | 1 | a0001c0001t0004g0158 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.463+4667T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64580571 | ||||||
| chr5:64580582
|
A | C | 1 | a0001c0001t0006g0086 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.463+4678A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64580582 | ||||||
| chr5:64580757
|
G | T | 1 | a0001c0001t0001g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.463+4853G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64580757 | ||||||
| chr5:64581369
|
A | G | 69 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0047others(66): Show | 69 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.463+5465A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64581369 | ||||||
| chr5:64581498
|
A | G | 69 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0047others(66): Show | 69 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.463+5594A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64581498 | ||||||
| chr5:64581685
|
C | T | 72 | a0001c0001t0001g0021a0001c0001t0001g0214a0001c0001t0001g0269others(69): Show | 74 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.463+5781C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64581685 | ||||||
| chr5:64581764
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.463+5860T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64581764 | ||||||
| chr5:64581795
|
G | A | 1 | a0001c0001t0006g0086 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.463+5891G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64581795 | ||||||
| chr5:64581904
|
C | A | 192 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0030others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.463+6000C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64581904 | ||||||
| chr5:64581926
|
G | A | 4 | a0001c0001t0015g0017a0002c0002t0001g0012a0002c0002t0001g0095others(1): Show | 4 | HG01884.hp1 HG03041.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+6022G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64581926 | ||||||
| chr5:64582089
|
A | T | 117 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0030others(114): Show | 121 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(118): Show |
intron_variant | MODIFIER | c.463+6185A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64582089 | ||||||
| chr5:64582092
|
A | C | 1 | a0001c0001t0004g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.463+6188A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64582092 | ||||||
| chr5:64582487
|
C | T | 2 | a0002c0002t0003g0170a0002c0002t0003g0171 | 2 | NA18939.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.463+6583C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64582487 | ||||||
| chr5:64582502
|
G | C | 3 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0166 | 3 | NA18965.hp1 NA18981.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.463+6598G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64582502 | ||||||
| chr5:64582686
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.463+6782T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64582686 | ||||||
| chr5:64582785
|
G | T | 4 | a0001c0001t0001g0053a0001c0001t0001g0058a0001c0001t0001g0067others(1): Show | 4 | HG02145.hp1 HG02572.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+6881G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64582785 | ||||||
| chr5:64582902
|
C | A | 1 | a0001c0001t0006g0086 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.463+6998C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64582902 | ||||||
| chr5:64582976
|
A | G | 17 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0075others(14): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.463+7072A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64582976 | ||||||
| chr5:64583120
|
G | C | 1 | a0001c0001t0004g0223 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.463+7216G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64583120 | ||||||
| chr5:64583123
|
C | G | 1 | a0001c0001t0001g0106 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.463+7219C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64583123 | ||||||
| chr5:64583140
|
T | C | 119 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0030others(116): Show | 123 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.463+7236T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64583140 | ||||||
| chr5:64583368
|
G | A | 1 | a0001c0001t0006g0086 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.463+7464G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64583368 | ||||||
| chr5:64583771
|
C | T | 3 | a0001c0001t0004g0254a0001c0001t0004g0255a0001c0001t0011g0013 | 3 | HG02451.hp1 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.463+7867C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64583771 | ||||||
| chr5:64583794
|
A | G | 1 | a0001c0001t0006g0086 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.463+7890A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64583794 | ||||||
| chr5:64583804
|
T | G | 1 | a0001c0001t0002g0160 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.463+7900T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64583804 | ||||||
| chr5:64583805
|
T | C | 1 | a0001c0001t0002g0160 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.463+7901T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64583805 | ||||||
| chr5:64584383
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.463+8479A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64584383 | ||||||
| chr5:64584487
|
G | A | 1 | a0001c0001t0002g0166 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.463+8583G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64584487 | ||||||
| chr5:64584494
|
T | A | 171 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0030others(168): Show | 175 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.463+8590T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64584494 | ||||||
| chr5:64584568
|
C | T | 174 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0030others(171): Show | 178 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.463+8664C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64584568 | ||||||
| chr5:64584671
|
G | C | 23 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0046others(20): Show | 25 | HG00099.hp2 HG00741.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.463+8767G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64584671 | ||||||
| chr5:64584689
|
C | T | 1 | a0001c0001t0005g0136 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.463+8785C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64584689 | ||||||
| chr5:64585015
|
C | T | 62 | a0001c0001t0001g0021a0001c0001t0001g0214a0001c0001t0001g0269others(59): Show | 63 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.463+9111C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64585015 | ||||||
| chr5:64585016
|
G | A | 4 | a0001c0001t0001g0053a0001c0001t0001g0058a0001c0001t0001g0067others(1): Show | 4 | HG02145.hp1 HG02572.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+9112G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64585016 | ||||||
| chr5:64585052
|
G | A | 22 | a0001c0001t0001g0001a0001c0001t0001g0052a0001c0001t0001g0075others(19): Show | 24 | HG01109.hp1 HG01978.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.463+9148G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64585052 | ||||||
| chr5:64585076
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.463+9172T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64585076 | ||||||
| chr5:64585124
|
G | A | 63 | a0001c0001t0001g0021a0001c0001t0001g0214a0001c0001t0001g0269others(60): Show | 64 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.463+9220G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64585124 | ||||||
| chr5:64585184
|
T | C | 164 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0035others(161): Show | 166 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(163): Show |
intron_variant | MODIFIER | c.463+9280T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64585184 | ||||||
| chr5:64585328
|
T | C | 11 | a0001c0001t0001g0177a0002c0002t0001g0090a0002c0002t0001g0091others(8): Show | 11 | HG01167.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.464-9382T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64585328 | ||||||
| chr5:64585391
|
C | T | 5 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0006g0087others(2): Show | 5 | HG01978.hp1 HG02257.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.464-9319C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64585391 | ||||||
| chr5:64585660
|
G | A | 1 | a0002c0002t0001g0185 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.464-9050G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64585660 | ||||||
| chr5:64585690
|
A | G | 100 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0052others(97): Show | 102 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.464-9020A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64585690 | ||||||
| chr5:64585691
|
C | G | 3 | a0001c0001t0001g0034a0001c0001t0008g0257a0001c0001t0021g0010 | 3 | HG01109.hp1 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.464-9019C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64585691 | ||||||
| chr5:64585771
|
G | A | 3 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0225 | 3 | HG02602.hp1 HG02738.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.464-8939G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64585771 | ||||||
| chr5:64585933
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.464-8777C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64585933 | ||||||
| chr5:64586029
|
A | G | 2 | a0001c0001t0013g0008a0001c0001t0013g0009 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.464-8681A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64586029 | ||||||
| chr5:64586038
|
T | C | 3 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0006g0187 | 3 | HG03139.hp2 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.464-8672T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64586038 | ||||||
| chr5:64586308
|
C | T | 1 | a0001c0001t0005g0272 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.464-8402C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64586308 | ||||||
| chr5:64586316
|
G | A | 10 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0004g0254others(7): Show | 10 | HG01109.hp1 HG01978.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.464-8394G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64586316 | ||||||
| chr5:64586320
|
G | A | 15 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0076others(12): Show | 17 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.464-8390G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64586320 | ||||||
| chr5:64586322
|
C | G | 4 | a0001c0001t0002g0241a0001c0001t0002g0246a0001c0001t0002g0247others(1): Show | 4 | NA18967.hp2 NA19064.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.464-8388C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64586322 | ||||||
| chr5:64586359
|
A | G | 1 | a0001c0001t0004g0268 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.464-8351A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64586359 | ||||||
| chr5:64586420
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.464-8290T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64586420 | ||||||
| chr5:64586463
|
T | C | 100 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0052others(97): Show | 102 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.464-8247T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64586463 | ||||||
| chr5:64586538
|
C | T | 1 | a0002c0002t0003g0129 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.464-8172C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64586538 | ||||||
| chr5:64586577
|
A | G | 100 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0052others(97): Show | 102 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.464-8133A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64586577 | ||||||
| chr5:64586666
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0109 | 2 | HG00741.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.464-8044C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64586666 | ||||||
| chr5:64586743
|
T | C | 16 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0076others(13): Show | 18 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.464-7967T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64586743 | ||||||
| chr5:64586754
|
AATAAATT others(28): Show |
A | 1 | a0001c0001t0002g0250 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.464-7954_464-7920d others(37): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 64586754 | |||||
| chr5:64586839
|
C | A | 100 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0052others(97): Show | 102 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.464-7871C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64586839 | ||||||
| chr5:64586872
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.464-7838C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64586872 | ||||||
| chr5:64586898
|
TGAAAG | T | 100 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0052others(97): Show | 102 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.464-7808_464-7804d others(7): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 64586898 | |||||
| chr5:64586916
|
A | G | 3 | a0001c0001t0004g0015a0001c0001t0004g0036a0001c0001t0004g0037 | 3 | HG02451.hp2 HG02572.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.464-7794A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64586916 | ||||||
| chr5:64586983
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.464-7727G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64586983 | ||||||
| chr5:64587033
|
G | A | 1 | a0001c0001t0019g0226 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.464-7677G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64587033 | ||||||
| chr5:64587115
|
G | A | 2 | a0001c0001t0013g0008a0001c0001t0013g0009 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.464-7595G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64587115 | ||||||
| chr5:64587158
|
C | A | 3 | a0001c0001t0002g0208a0001c0001t0002g0220a0003c0004t0002g0215 | 3 | HG02273.hp1 HG02293.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.464-7552C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64587158 | ||||||
| chr5:64587419
|
G | A | 3 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0006g0187 | 3 | HG03139.hp2 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.464-7291G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64587419 | ||||||
| chr5:64587466
|
A | G | 99 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0052others(96): Show | 101 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.464-7244A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64587466 | ||||||
| chr5:64587485
|
A | G | 2 | a0001c0001t0008g0257a0001c0001t0021g0010 | 2 | HG01109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.464-7225A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64587485 | ||||||
| chr5:64587523
|
T | C | 99 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0052others(96): Show | 101 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.464-7187T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64587523 | ||||||
| chr5:64587637
|
T | C | 72 | a0001c0001t0001g0021a0001c0001t0001g0214a0001c0001t0001g0269others(69): Show | 74 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.464-7073T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64587637 | ||||||
| chr5:64587660
|
T | C | 100 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0052others(97): Show | 102 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.464-7050T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64587660 | ||||||
| chr5:64587725
|
G | C | 11 | a0001c0001t0001g0177a0002c0002t0001g0090a0002c0002t0001g0091others(8): Show | 11 | HG01167.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.464-6985G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64587725 | ||||||
| chr5:64587766
|
C | T | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.464-6944C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64587766 | ||||||
| chr5:64587821
|
T | G | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.464-6889T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64587821 | ||||||
| chr5:64587911
|
G | A | 99 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0052others(96): Show | 101 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.464-6799G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64587911 | ||||||
| chr5:64587960
|
C | T | 99 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0052others(96): Show | 101 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.464-6750C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64587960 | ||||||
| chr5:64588034
|
T | C | 100 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0052others(97): Show | 102 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.464-6676T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64588034 | ||||||
| chr5:64588250
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.464-6460C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64588250 | ||||||
| chr5:64588271
|
T | C | 2 | a0001c0001t0004g0065a0001c0001t0004g0245 | 2 | NA18612.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.464-6439T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64588271 | ||||||
| chr5:64588552
|
A | C | 1 | a0002c0002t0003g0147 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.464-6158A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64588552 | ||||||
| chr5:64588553
|
C | A | 1 | a0002c0002t0003g0147 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.464-6157C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64588553 | ||||||
| chr5:64588655
|
T | A | 1 | a0001c0001t0011g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.464-6055T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64588655 | ||||||
| chr5:64588813
|
T | TA | 19 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0177others(16): Show | 19 | HG01167.hp1 HG01884.hp2 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.464-5890dupA | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 64588813 | |||||
| chr5:64588814
|
A | T | 8 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0043others(5): Show | 9 | HG02258.hp1 HG02965.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.464-5896A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64588814 | ||||||
| chr5:64588847
|
A | G | 8 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0043others(5): Show | 9 | HG02258.hp1 HG02965.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.464-5863A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64588847 | ||||||
| chr5:64588854
|
A | G | 1 | a0001c0001t0002g0216 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.464-5856A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64588854 | ||||||
| chr5:64588892
|
T | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0029others(210): Show | 219 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(216): Show |
intron_variant | MODIFIER | c.464-5818T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64588892 | ||||||
| chr5:64588904
|
A | G | 3 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0006g0187 | 3 | HG03139.hp2 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.464-5806A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64588904 | ||||||
| chr5:64588910
|
G | A | 1 | a0001c0001t0002g0153 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.464-5800G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64588910 | ||||||
| chr5:64588966
|
G | C | 2 | a0001c0001t0013g0008a0001c0001t0013g0009 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.464-5744G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64588966 | ||||||
| chr5:64588974
|
A | G | 19 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0177others(16): Show | 19 | HG01167.hp1 HG01884.hp2 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.464-5736A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64588974 | ||||||
| chr5:64589140
|
CA | C | 8 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0043others(5): Show | 9 | HG02258.hp1 HG02965.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.464-5562delA | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 64589140 | |||||
| chr5:64589153
|
G | A | 2 | a0001c0001t0013g0008a0001c0001t0013g0009 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.464-5557G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64589153 | ||||||
| chr5:64589226
|
G | A | 16 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0055others(13): Show | 16 | HG00099.hp1 HG00642.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.464-5484G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64589226 | ||||||
| chr5:64589381
|
A | G | 69 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0047others(66): Show | 69 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.464-5329A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64589381 | ||||||
| chr5:64589476
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.464-5234G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64589476 | ||||||
| chr5:64589666
|
G | T | 1 | a0002c0002t0003g0062 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.464-5044G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64589666 | ||||||
| chr5:64589921
|
A | G | 1 | a0001c0001t0002g0240 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.464-4789A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64589921 | ||||||
| chr5:64589924
|
CA | C | 50 | a0001c0001t0001g0047a0001c0001t0001g0053a0001c0001t0001g0057others(47): Show | 51 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.464-4770delA | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 64589924 | |||||
| chr5:64590103
|
A | T | 1 | a0001c0001t0004g0038 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.464-4607A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64590103 | ||||||
| chr5:64590111
|
T | A | 1 | a0002c0002t0003g0051 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.464-4599T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64590111 | ||||||
| chr5:64590330
|
G | A | 1 | a0001c0001t0019g0226 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.464-4380G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64590330 | ||||||
| chr5:64590499
|
G | A | 1 | a0001c0001t0006g0087 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.464-4211G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64590499 | ||||||
| chr5:64590604
|
T | C | 4 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0006g0087others(1): Show | 4 | HG01978.hp1 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-4106T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64590604 | ||||||
| chr5:64590757
|
TATC | T | 19 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0177others(16): Show | 19 | HG01167.hp1 HG01884.hp2 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.464-3950_464-3948d others(5): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 64590757 | |||||
| chr5:64590888
|
G | A | 3 | a0001c0001t0001g0100a0001c0001t0008g0257a0001c0001t0021g0010 | 3 | HG01109.hp1 HG01978.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.464-3822G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64590888 | ||||||
| chr5:64591014
|
T | C | 1 | a0001c0001t0004g0139 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.464-3696T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64591014 | ||||||
| chr5:64591098
|
A | G | 2 | a0001c0001t0008g0257a0001c0001t0021g0010 | 2 | HG01109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.464-3612A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64591098 | ||||||
| chr5:64591266
|
A | C | 1 | a0002c0002t0001g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.464-3444A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64591266 | ||||||
| chr5:64591348
|
A | C | 3 | a0002c0002t0001g0221a0002c0002t0001g0222a0002c0002t0001g0232 | 3 | HG01123.hp1 HG03490.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.464-3362A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64591348 | ||||||
| chr5:64591356
|
A | C | 19 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0177others(16): Show | 19 | HG01167.hp1 HG01884.hp2 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.464-3354A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64591356 | ||||||
| chr5:64591407
|
T | G | 2 | a0001c0001t0013g0008a0001c0001t0013g0009 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.464-3303T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64591407 | ||||||
| chr5:64591411
|
A | T | 2 | a0001c0001t0013g0008a0001c0001t0013g0009 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.464-3299A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64591411 | ||||||
| chr5:64592468
|
C | T | 5 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0006g0187others(2): Show | 5 | HG02647.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.464-2242C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64592468 | ||||||
| chr5:64592733
|
C | G | 1 | a0001c0001t0006g0086 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.464-1977C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64592733 | ||||||
| chr5:64592800
|
G | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0052others(109): Show | 116 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(113): Show |
intron_variant | MODIFIER | c.464-1910G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64592800 | ||||||
| chr5:64592823
|
A | G | 3 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0006g0187 | 3 | HG03139.hp2 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.464-1887A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64592823 | ||||||
| chr5:64592834
|
G | C | 8 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0043others(5): Show | 9 | HG02258.hp1 HG02965.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.464-1876G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64592834 | ||||||
| chr5:64592893
|
C | G | 5 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0006g0187others(2): Show | 5 | HG02647.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.464-1817C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64592893 | ||||||
| chr5:64593008
|
A | C | 73 | a0001c0001t0001g0021a0001c0001t0001g0214a0001c0001t0001g0269others(70): Show | 75 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.464-1702A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64593008 | ||||||
| chr5:64593184
|
C | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0029others(207): Show | 216 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.464-1526C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64593184 | ||||||
| chr5:64593310
|
C | T | 1 | a0001c0001t0011g0013 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.464-1400C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64593310 | ||||||
| chr5:64593469
|
T | C | 2 | a0001c0001t0002g0250a0001c0001t0002g0253 | 2 | NA18939.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.464-1241T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64593469 | ||||||
| chr5:64593727
|
G | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0029others(130): Show | 139 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(136): Show |
intron_variant | MODIFIER | c.464-983G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64593727 | ||||||
| chr5:64593826
|
C | A | 1 | a0001c0001t0001g0068 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.464-884C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64593826 | ||||||
| chr5:64593842
|
A | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0029others(209): Show | 218 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(215): Show |
intron_variant | MODIFIER | c.464-868A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64593842 | ||||||
| chr5:64593862
|
C | T | 1 | a0001c0001t0006g0086 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.464-848C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64593862 | ||||||
| chr5:64593873
|
C | A | 27 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0076others(24): Show | 29 | HG01167.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.464-837C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64593873 | ||||||
| chr5:64593874
|
C | G | 3 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0006g0187 | 3 | HG03139.hp2 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.464-836C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64593874 | ||||||
| chr5:64593922
|
T | C | 2 | a0001c0001t0013g0008a0001c0001t0013g0009 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.464-788T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64593922 | ||||||
| chr5:64593956
|
A | C | 27 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0076others(24): Show | 29 | HG01167.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.464-754A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64593956 | ||||||
| chr5:64594115
|
C | T | 15 | a0001c0001t0001g0040a0001c0001t0001g0055a0001c0001t0001g0060others(12): Show | 15 | HG00099.hp1 HG00642.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.464-595C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64594115 | ||||||
| chr5:64594230
|
C | T | 1 | a0002c0002t0003g0199 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.464-480C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64594230 | ||||||
| chr5:64594245
|
G | C | 15 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0076others(12): Show | 17 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.464-465G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64594245 | ||||||
| chr5:64594306
|
A | C | 73 | a0001c0001t0001g0021a0001c0001t0001g0214a0001c0001t0001g0269others(70): Show | 75 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.464-404A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64594306 | ||||||
| chr5:64594384
|
C | T | 5 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0006g0187others(2): Show | 5 | HG02647.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.464-326C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64594384 | ||||||
| chr5:64594495
|
G | A | 5 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0006g0187others(2): Show | 5 | HG02647.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.464-215G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64594495 | ||||||
| chr5:64594508
|
T | C | 31 | a0001c0001t0001g0001a0001c0001t0001g0052a0001c0001t0001g0075others(28): Show | 33 | HG01167.hp1 HG01884.hp2 HG01978.hp1 others(30): Show |
intron_variant | MODIFIER | c.464-202T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64594508 | ||||||
| chr5:64594560
|
C | T | 211 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0029others(208): Show | 217 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.464-150C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64594560 | ||||||
| chr5:64594670
|
C | A | 1 | a0001c0001t0013g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.464-40C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 3/5 | chr5 | 64594670 | ||||||
| chr5:64594918
|
C | T | 31 | a0001c0001t0001g0001a0001c0001t0001g0052a0001c0001t0001g0075others(28): Show | 33 | HG01167.hp1 HG01884.hp2 HG01978.hp1 others(30): Show |
intron_variant | MODIFIER | c.611+61C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 4/5 | chr5 | 64594918 | ||||||
| chr5:64594980
|
G | T | 4 | a0001c0001t0001g0047a0001c0001t0001g0057a0001c0001t0001g0059others(1): Show | 4 | HG00738.hp1 HG01106.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.611+123G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 4/5 | chr5 | 64594980 | ||||||
| chr5:64595315
|
T | G | 1 | a0001c0001t0004g0274 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.611+458T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 4/5 | chr5 | 64595315 | ||||||
| chr5:64595319
|
T | C | 67 | a0001c0001t0001g0021a0001c0001t0001g0125a0001c0001t0001g0214others(64): Show | 68 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.611+462T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 4/5 | chr5 | 64595319 | ||||||
| chr5:64595324
|
G | C | 31 | a0001c0001t0001g0001a0001c0001t0001g0052a0001c0001t0001g0075others(28): Show | 33 | HG01167.hp1 HG01884.hp2 HG01978.hp1 others(30): Show |
intron_variant | MODIFIER | c.611+467G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 4/5 | chr5 | 64595324 | ||||||
| chr5:64595539
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.611+682A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 4/5 | chr5 | 64595539 | ||||||
| chr5:64595844
|
C | A | 1 | a0001c0001t0001g0063 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.611+987C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 4/5 | chr5 | 64595844 | ||||||
| chr5:64595984
|
C | T | 1 | a0001c0001t0008g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.611+1127C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 4/5 | chr5 | 64595984 | ||||||
| chr5:64596317
|
G | T | 1 | a0001c0001t0002g0216 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.611+1460G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 4/5 | chr5 | 64596317 | ||||||
| chr5:64596425
|
C | G | 17 | a0001c0001t0001g0035a0001c0001t0001g0046a0001c0001t0001g0074others(14): Show | 17 | HG00741.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.611+1568C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 4/5 | chr5 | 64596425 | ||||||
| chr5:64596506
|
A | C | 39 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0024others(36): Show | 39 | HG00741.hp2 HG01109.hp1 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.611+1649A>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 4/5 | chr5 | 64596506 | ||||||
| chr5:64596520
|
C | G | 1 | a0001c0001t0001g0053 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.611+1663C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 4/5 | chr5 | 64596520 | ||||||
| chr5:64596885
|
T | A | 13 | a0001c0001t0001g0035a0001c0001t0001g0046a0001c0001t0001g0074others(10): Show | 13 | HG00741.hp2 HG02145.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.612-1480T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 4/5 | chr5 | 64596885 | ||||||
| chr5:64597201
|
G | C | 1 | a0001c0001t0002g0020 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.612-1164G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 4/5 | chr5 | 64597201 | ||||||
| chr5:64597247
|
T | C | 1 | a0001c0001t0001g0237 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.612-1118T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 4/5 | chr5 | 64597247 | ||||||
| chr5:64597463
|
T | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(46): Show | 51 | HG00738.hp1 HG01106.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.612-902T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 4/5 | chr5 | 64597463 | ||||||
| chr5:64597475
|
T | C | 51 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(48): Show | 53 | HG00738.hp1 HG01106.hp1 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.612-890T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 4/5 | chr5 | 64597475 | ||||||
| chr5:64597562
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.612-803T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 4/5 | chr5 | 64597562 | ||||||
| chr5:64597727
|
G | A | 38 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0004g0015others(35): Show | 38 | HG00558.hp2 HG00621.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.612-638G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 4/5 | chr5 | 64597727 | ||||||
| chr5:64597950
|
C | T | 15 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0067others(12): Show | 17 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.612-415C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 4/5 | chr5 | 64597950 | ||||||
| chr5:64597984
|
C | T | 11 | a0002c0002t0001g0090a0002c0002t0001g0091a0002c0002t0001g0092others(8): Show | 11 | HG01167.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.612-381C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 4/5 | chr5 | 64597984 | ||||||
| chr5:64598255
|
T | C | 2 | a0001c0001t0001g0034a0001c0001t0001g0053 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.612-110T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 4/5 | chr5 | 64598255 | ||||||
| chr5:64598653
|
G | T | 2 | a0001c0001t0013g0008a0001c0001t0013g0009 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.682+218G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64598653 | ||||||
| chr5:64598661
|
T | C | 2 | a0001c0001t0013g0008a0001c0001t0013g0009 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.682+226T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64598661 | ||||||
| chr5:64598851
|
A | G | 2 | a0001c0001t0002g0195a0001c0001t0002g0196 | 2 | HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.682+416A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64598851 | ||||||
| chr5:64598923
|
C | A | 1 | a0001c0001t0001g0029 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.682+488C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64598923 | ||||||
| chr5:64599012
|
A | G | 3 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0166 | 3 | NA18965.hp1 NA18981.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.682+577A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64599012 | ||||||
| chr5:64599169
|
C | G | 2 | a0001c0001t0013g0008a0001c0001t0013g0009 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.682+734C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64599169 | ||||||
| chr5:64599447
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.682+1012T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64599447 | ||||||
| chr5:64599530
|
C | T | 142 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0040others(139): Show | 144 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(141): Show |
intron_variant | MODIFIER | c.682+1095C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64599530 | ||||||
| chr5:64599559
|
C | G | 3 | a0001c0001t0008g0007a0001c0001t0008g0257a0001c0001t0021g0010 | 3 | HG01109.hp1 HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.682+1124C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64599559 | ||||||
| chr5:64599593
|
C | A | 2 | a0001c0001t0013g0008a0001c0001t0013g0009 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.682+1158C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64599593 | ||||||
| chr5:64599709
|
T | C | 3 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0225 | 3 | HG02602.hp1 HG02738.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.682+1274T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64599709 | ||||||
| chr5:64599983
|
A | G | 15 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0067others(12): Show | 17 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.682+1548A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64599983 | ||||||
| chr5:64600397
|
T | A | 25 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0024others(22): Show | 25 | HG00738.hp1 HG01106.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.682+1962T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64600397 | ||||||
| chr5:64600724
|
G | T | 1 | a0001c0001t0016g0261 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.682+2289G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64600724 | ||||||
| chr5:64600760
|
C | T | 1 | a0002c0002t0001g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.682+2325C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64600760 | ||||||
| chr5:64600831
|
A | G | 3 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0006g0086 | 3 | HG01891.hp1 HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.682+2396A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64600831 | ||||||
| chr5:64600872
|
A | G | 3 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0006g0086 | 3 | HG01891.hp1 HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.682+2437A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64600872 | ||||||
| chr5:64600941
|
C | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(48): Show | 53 | HG00738.hp1 HG01106.hp1 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.682+2506C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64600941 | ||||||
| chr5:64601002
|
A | G | 1 | a0002c0002t0003g0119 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.682+2567A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64601002 | ||||||
| chr5:64601357
|
T | C | 4 | a0001c0001t0001g0021a0001c0001t0001g0100a0001c0001t0001g0125others(1): Show | 4 | HG00099.hp2 HG01256.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.682+2922T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64601357 | ||||||
| chr5:64601581
|
C | T | 1 | a0001c0001t0004g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.682+3146C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64601581 | ||||||
| chr5:64601628
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.682+3193G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64601628 | ||||||
| chr5:64601650
|
G | A | 1 | a0001c0001t0006g0086 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.682+3215G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64601650 | ||||||
| chr5:64601959
|
C | T | 1 | a0002c0002t0003g0098 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.682+3524C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64601959 | ||||||
| chr5:64602114
|
C | G | 25 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0024others(22): Show | 25 | HG00738.hp1 HG01106.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.682+3679C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64602114 | ||||||
| chr5:64602152
|
T | C | 16 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0058others(13): Show | 18 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.682+3717T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64602152 | ||||||
| chr5:64602347
|
A | T | 1 | a0001c0001t0002g0208 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.682+3912A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64602347 | ||||||
| chr5:64602374
|
G | A | 3 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0006g0086 | 3 | HG01891.hp1 HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.682+3939G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64602374 | ||||||
| chr5:64602411
|
AT | A | 3 | a0001c0001t0011g0013a0001c0001t0011g0014a0001c0001t0015g0017 | 3 | HG01884.hp1 HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.682+3978delT | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 64602411 | |||||
| chr5:64602474
|
G | C | 2 | a0001c0001t0013g0008a0001c0001t0013g0009 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.682+4039G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64602474 | ||||||
| chr5:64602622
|
C | G | 3 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0006g0086 | 3 | HG01891.hp1 HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.682+4187C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64602622 | ||||||
| chr5:64602654
|
C | G | 3 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0006g0187 | 3 | HG03139.hp2 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.682+4219C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64602654 | ||||||
| chr5:64602714
|
A | G | 3 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0006g0086 | 3 | HG01891.hp1 HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.682+4279A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64602714 | ||||||
| chr5:64602730
|
A | T | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0138others(2): Show | 5 | HG01175.hp1 HG01934.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.682+4295A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64602730 | ||||||
| chr5:64602832
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.682+4397T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64602832 | ||||||
| chr5:64602835
|
T | A | 16 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0058others(13): Show | 18 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.682+4400T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64602835 | ||||||
| chr5:64603036
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.682+4601C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64603036 | ||||||
| chr5:64603114
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.682+4679G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64603114 | ||||||
| chr5:64603222
|
A | AT | 28 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0024others(25): Show | 28 | HG00738.hp1 HG01106.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.682+4788dupT | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 64603222 | |||||
| chr5:64603778
|
G | A | 1 | a0001c0001t0002g0114 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.682+5343G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64603778 | ||||||
| chr5:64603807
|
A | G | 16 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0058others(13): Show | 18 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.683-5354A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64603807 | ||||||
| chr5:64603841
|
A | G | 1 | a0001c0001t0002g0096 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.683-5320A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64603841 | ||||||
| chr5:64603893
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.683-5268C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64603893 | ||||||
| chr5:64603948
|
T | A | 3 | a0001c0001t0011g0013a0001c0001t0011g0014a0001c0001t0015g0017 | 3 | HG01884.hp1 HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.683-5213T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64603948 | ||||||
| chr5:64604097
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.683-5064T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64604097 | ||||||
| chr5:64604205
|
G | A | 2 | a0001c0001t0011g0013a0001c0001t0011g0014 | 2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.683-4956G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64604205 | ||||||
| chr5:64604238
|
G | A | 1 | a0001c0001t0002g0253 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.683-4923G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64604238 | ||||||
| chr5:64604335
|
C | G | 29 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0024others(26): Show | 29 | HG00738.hp1 HG01106.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.683-4826C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64604335 | ||||||
| chr5:64604336
|
C | A | 28 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0024others(25): Show | 28 | HG00738.hp1 HG01106.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.683-4825C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64604336 | ||||||
| chr5:64604336
|
C | G | 2 | a0002c0002t0003g0170a0002c0002t0003g0171 | 2 | NA18939.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.683-4825C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64604336 | ||||||
| chr5:64604406
|
T | G | 1 | a0001c0001t0002g0018 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.683-4755T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64604406 | ||||||
| chr5:64604424
|
T | A | 1 | a0002c0002t0003g0249 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.683-4737T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64604424 | ||||||
| chr5:64604532
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.683-4629C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64604532 | ||||||
| chr5:64604671
|
G | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0021others(190): Show | 197 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(194): Show |
intron_variant | MODIFIER | c.683-4490G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64604671 | ||||||
| chr5:64604716
|
C | G | 68 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0018others(65): Show | 70 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.683-4445C>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64604716 | ||||||
| chr5:64604717
|
T | A | 3 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0006g0086 | 3 | HG01891.hp1 HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.683-4444T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64604717 | ||||||
| chr5:64604804
|
CA | C | 16 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0058others(13): Show | 18 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.683-4353delA | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 64604804 | |||||
| chr5:64604895
|
T | C | 52 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(49): Show | 54 | HG00738.hp1 HG01106.hp1 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.683-4266T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64604895 | ||||||
| chr5:64604958
|
C | T | 5 | a0001c0001t0001g0046a0001c0001t0001g0108a0001c0001t0001g0109others(2): Show | 5 | HG00741.hp2 HG02486.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.683-4203C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64604958 | ||||||
| chr5:64604968
|
G | A | 3 | a0002c0002t0001g0090a0002c0002t0001g0091a0002c0002t0001g0092 | 3 | HG02280.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.683-4193G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64604968 | ||||||
| chr5:64604986
|
G | A | 52 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(49): Show | 54 | HG00738.hp1 HG01106.hp1 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.683-4175G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64604986 | ||||||
| chr5:64605027
|
T | C | 1 | a0001c0001t0002g0263 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.683-4134T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64605027 | ||||||
| chr5:64605028
|
T | A | 3 | a0001c0001t0002g0018a0001c0001t0002g0216a0002c0002t0006g0085 | 3 | HG03225.hp2 HG03486.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.683-4133T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64605028 | ||||||
| chr5:64605056
|
T | C | 2 | a0002c0002t0003g0134a0002c0002t0003g0161 | 2 | NA18612.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.683-4105T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64605056 | ||||||
| chr5:64605099
|
C | A | 3 | a0001c0001t0008g0007a0001c0001t0008g0257a0001c0001t0021g0010 | 3 | HG01109.hp1 HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.683-4062C>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64605099 | ||||||
| chr5:64605477
|
C | T | 87 | a0001c0001t0001g0040a0001c0001t0001g0055a0001c0001t0001g0060others(84): Show | 89 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.683-3684C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64605477 | ||||||
| chr5:64605574
|
T | C | 1 | a0001c0001t0006g0087 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.683-3587T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64605574 | ||||||
| chr5:64605594
|
T | G | 2 | a0001c0001t0001g0060a0001c0001t0001g0106 | 2 | NA18950.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.683-3567T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64605594 | ||||||
| chr5:64605627
|
T | G | 1 | a0001c0001t0004g0016 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.683-3534T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64605627 | ||||||
| chr5:64605710
|
C | T | 1 | a0001c0001t0011g0013 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.683-3451C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64605710 | ||||||
| chr5:64605882
|
G | GTATATAT others(30): Show |
1 | a0001c0001t0002g0018 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.683-3264_683-3263i others(39): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 64605882 | |||||
| chr5:64605882
|
G | GTATATAT others(28): Show |
81 | a0001c0001t0001g0100a0001c0001t0001g0168a0001c0001t0001g0258others(78): Show | 83 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.683-3164_683-3130d others(37): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 64605882 | |||||
| chr5:64605882
|
G | GTATATAT others(98): Show |
1 | a0001c0001t0004g0268 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.683-3234_683-3130d others(107): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 64605882 | |||||
| chr5:64605882
|
G | GTATATAT others(133): Show |
1 | a0001c0001t0001g0052 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.683-3269_683-3130d others(142): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 64605882 | |||||
| chr5:64605882
|
GTATATAT others(28): Show |
G | 4 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0001g0125others(1): Show | 4 | HG00099.hp2 HG01891.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-3164_683-3130d others(37): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 64605882 | |||||
| chr5:64605916
|
C | CAT | 15 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0067others(12): Show | 17 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.683-3236_683-3235d others(4): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 64605916 | |||||
| chr5:64605918
|
T | TATATATA others(61): Show |
1 | a0001c0001t0001g0111 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.683-3234_683-3167d others(70): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 64605918 | |||||
| chr5:64605918
|
TATATATA others(26): Show |
T | 1 | a0001c0001t0001g0058 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.683-3234_683-3202d others(35): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 64605918 | |||||
| chr5:64605925
|
A | T | 25 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0024others(22): Show | 25 | HG00738.hp1 HG01106.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.683-3236A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64605925 | ||||||
| chr5:64605951
|
CAT | C | 3 | a0001c0001t0008g0007a0001c0001t0008g0257a0001c0001t0021g0010 | 3 | HG01109.hp1 HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.683-3201_683-3200d others(4): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 64605951 | |||||
| chr5:64605951
|
CATATATA others(65): Show |
C | 1 | a0001c0001t0001g0148 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.683-3199_683-3128d others(74): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 64605951 | |||||
| chr5:64605953
|
T | TATATATA others(26): Show |
16 | a0001c0001t0001g0040a0001c0001t0001g0055a0001c0001t0001g0060others(13): Show | 16 | HG00099.hp1 HG00642.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.683-3199_683-3167d others(35): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 64605953 | |||||
| chr5:64605960
|
A | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0061 | 2 | HG01891.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.683-3201A>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64605960 | ||||||
| chr5:64605986
|
CATATATA others(30): Show |
C | 27 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0024others(24): Show | 27 | HG00738.hp1 HG01106.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.683-3164_683-3128d others(39): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 64605986 | |||||
| chr5:64605986
|
CATATATA others(32): Show |
C | 3 | a0001c0001t0008g0007a0001c0001t0008g0257a0001c0001t0021g0010 | 3 | HG01109.hp1 HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.683-3164_683-3126d others(41): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 64605986 | |||||
| chr5:64606021
|
C | CATATATA others(30): Show |
6 | a0001c0001t0002g0219a0001c0001t0002g0239a0001c0001t0002g0241others(3): Show | 6 | HG00639.hp1 HG03491.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.683-3130_683-3129i others(39): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 64606021 | |||||
| chr5:64606025
|
T | TATATATG others(24): Show |
2 | a0001c0001t0004g0254a0001c0001t0004g0255 | 2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.683-3130_683-3129i others(33): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 64606025 | |||||
| chr5:64606030
|
A | ATGC | 8 | a0001c0001t0001g0021a0001c0001t0002g0192a0001c0001t0004g0016others(5): Show | 8 | HG00639.hp2 HG01256.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.683-3130_683-3129i others(5): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 64606030 | |||||
| chr5:64606035
|
T | C | 1 | a0001c0001t0002g0153 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.683-3126T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64606035 | ||||||
| chr5:64606035
|
T | G | 2 | a0001c0001t0004g0084a0002c0002t0001g0159 | 2 | HG01081.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.683-3126T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64606035 | ||||||
| chr5:64606037
|
T | G | 25 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0046others(22): Show | 27 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.683-3124T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64606037 | ||||||
| chr5:64606039
|
T | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0034others(106): Show | 113 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.683-3122T>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64606039 | ||||||
| chr5:64606039
|
T | TGTATATC others(25): Show |
1 | a0001c0001t0004g0083 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.683-3122_683-3121i others(34): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64606039 | ||||||
| chr5:64606039
|
T | TGTATATC others(25): Show |
7 | a0001c0001t0001g0021a0001c0001t0002g0192a0001c0001t0004g0016others(4): Show | 7 | HG01256.hp1 HG01258.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.683-3122_683-3121i others(34): Show |
RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64606039 | ||||||
| chr5:64606041
|
G | T | 79 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0024others(76): Show | 81 | HG00423.hp1 HG00597.hp2 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.683-3120G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64606041 | ||||||
| chr5:64606043
|
G | T | 5 | a0001c0001t0001g0177a0001c0001t0002g0002a0001c0001t0002g0044others(2): Show | 6 | HG02647.hp1 HG03098.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.683-3118G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64606043 | ||||||
| chr5:64606051
|
G | C | 1 | a0001c0001t0006g0086 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.683-3110G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64606051 | ||||||
| chr5:64606326
|
C | CA | 273 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0021others(270): Show | 279 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.683-2832dupA | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 64606326 | |||||
| chr5:64606370
|
A | G | 3 | a0001c0001t0008g0007a0001c0001t0008g0257a0001c0001t0021g0010 | 3 | HG01109.hp1 HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.683-2791A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64606370 | ||||||
| chr5:64606375
|
C | T | 1 | a0001c0001t0002g0018 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.683-2786C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64606375 | ||||||
| chr5:64606376
|
T | C | 1 | a0001c0001t0002g0018 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.683-2785T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64606376 | ||||||
| chr5:64606377
|
C | T | 1 | a0001c0001t0002g0018 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.683-2784C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64606377 | ||||||
| chr5:64606408
|
G | A | 2 | a0001c0001t0013g0008a0001c0001t0013g0009 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.683-2753G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64606408 | ||||||
| chr5:64606480
|
A | G | 1 | a0002c0002t0003g0042 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.683-2681A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64606480 | ||||||
| chr5:64606534
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.683-2627G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64606534 | ||||||
| chr5:64606716
|
C | T | 3 | a0002c0002t0001g0221a0002c0002t0001g0222a0002c0002t0001g0232 | 3 | HG01123.hp1 HG03490.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.683-2445C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64606716 | ||||||
| chr5:64606998
|
C | CA | 68 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0018others(65): Show | 70 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.683-2162dupA | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 64606998 | |||||
| chr5:64607061
|
T | A | 1 | a0002c0002t0001g0012 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.683-2100T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64607061 | ||||||
| chr5:64607073
|
T | C | 19 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0058others(16): Show | 21 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.683-2088T>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64607073 | ||||||
| chr5:64607273
|
T | A | 28 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0024others(25): Show | 28 | HG00738.hp1 HG01106.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.683-1888T>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64607273 | ||||||
| chr5:64607321
|
A | G | 1 | a0002c0002t0003g0112 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.683-1840A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64607321 | ||||||
| chr5:64607354
|
G | A | 1 | a0002c0002t0003g0062 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.683-1807G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64607354 | ||||||
| chr5:64607399
|
G | T | 52 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(49): Show | 54 | HG00738.hp1 HG01106.hp1 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.683-1762G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64607399 | ||||||
| chr5:64607678
|
G | A | 1 | a0001c0001t0004g0223 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.683-1483G>A | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64607678 | ||||||
| chr5:64607756
|
G | C | 1 | a0002c0002t0001g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.683-1405G>C | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64607756 | ||||||
| chr5:64608574
|
C | T | 3 | a0001c0001t0011g0013a0001c0001t0011g0014a0001c0001t0015g0017 | 3 | HG01884.hp1 HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.683-587C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64608574 | ||||||
| chr5:64608584
|
A | G | 3 | a0001c0001t0011g0013a0001c0001t0011g0014a0001c0001t0015g0017 | 3 | HG01884.hp1 HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.683-577A>G | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64608584 | ||||||
| chr5:64608909
|
G | T | 1 | a0001c0001t0010g0019 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.683-252G>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64608909 | ||||||
| chr5:64608949
|
C | T | 1 | a0001c0001t0002g0198 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.683-212C>T | RGS7BP | ENSG00000186479.5 | transcript | ENST00000334025.3 | protein_coding | 5/5 | chr5 | 64608949 |