Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 5998 |
|---|---|
| ensemblid | ENSG00000138835.24 |
| hgncid | 9999 |
| symbol | RGS3 |
| name | regulator of G protein signaling 3 |
| refseq_nuc | NM_001394167.1 |
| refseq_prot | NP_001381096.1 |
| ensembl_nuc | ENST00000695401.1 |
| ensembl_prot | ENSP00000511882.1 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 113463727 |
| end | 113597738 |
| strand | + |
| ver | v1.2 |
| region | chr9:113463727-113597738 |
| region5000 | chr9:113458727-113602738 |
| regionname0 | RGS3_chr9_113463727_113597738 |
| regionname5000 | RGS3_chr9_113458727_113602738 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1086 | 132 | 41 | 30 | 39 | 5 | 15 | 25 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0002 | 0/0 | 1086 | 31 | 19 | 8 | 0 | 2 | 2 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0003 | 0/0 | 1086 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0004 | 0/0 | 1086 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0005 | 0/0 | 1086 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0006 | 0/0 | 1086 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0007 | 0/0 | 1086 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 3261 | 95 | 26 | 18 | 34 | 4 | 12 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| c0002 | 0/0 | 3261 | 21 | 6 | 8 | 5 | 1 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| c0003 | 0/0 | 3261 | 13 | 3 | 6 | 0 | 2 | 2 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| c0004 | 0/0 | 3261 | 8 | 6 | 2 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| c0005 | 0/0 | 3261 | 7 | 7 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| c0006 | 0/0 | 3261 | 6 | 6 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| c0007 | 0/1 | 3261 | 4 | 0 | 3 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| c0008 | 0/0 | 3261 | 2 | 2 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| c0009 | 0/0 | 3261 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| c0010 | 0/0 | 3261 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| c0011 | 0/0 | 3261 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| c0012 | 0/0 | 3261 | 1 | 0 | 0 | 0 | 1 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| c0013 | 0/0 | 3261 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| c0014 | 0/0 | 3261 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| c0015 | 0/0 | 3261 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| c0016 | 0/0 | 3261 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| c0017 | 0/0 | 3261 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| c0018 | 0/0 | 3261 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| c0019 | 0/0 | 3261 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| c0020 | 0/0 | 3261 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 862 | 109 | 32 | 24 | 36 | 2 | 14 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| t0002 | 1/0 | 862 | 30 | 15 | 8 | 0 | 3 | 3 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| t0003 | 0/0 | 862 | 13 | 11 | 2 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| t0004 | 0/0 | 862 | 6 | 0 | 1 | 3 | 1 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| t0005 | 0/0 | 862 | 4 | 0 | 2 | 0 | 2 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| t0006 | 0/0 | 862 | 4 | 3 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| t0007 | 0/0 | 862 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| t0008 | 0/0 | 862 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0059 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0087 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3261 | 95 | 26 | 18 | 34 | 4 | 12 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0001c0002 | 0/0 | 3261 | 21 | 6 | 8 | 5 | 1 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0001c0006 | 0/0 | 3261 | 6 | 6 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0001c0007 | 0/1 | 3261 | 4 | 0 | 3 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0001c0010 | 0/0 | 3261 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0001c0011 | 0/0 | 3261 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0001c0013 | 0/0 | 3261 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0001c0015 | 0/0 | 3261 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0001c0018 | 0/0 | 3261 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0001c0019 | 0/0 | 3261 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0002c0003 | 0/0 | 3261 | 13 | 3 | 6 | 0 | 2 | 2 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0002c0004 | 0/0 | 3261 | 8 | 6 | 2 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0002c0005 | 0/0 | 3261 | 7 | 7 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0002c0008 | 0/0 | 3261 | 2 | 2 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0002c0014 | 0/0 | 3261 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0003c0020 | 0/0 | 3261 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0004c0009 | 0/0 | 3261 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0005c0017 | 0/0 | 3261 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0006c0012 | 0/0 | 3261 | 1 | 0 | 0 | 0 | 1 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0007c0016 | 0/0 | 3261 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4122 | 69 | 15 | 12 | 31 | 1 | 10 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0001c0001t0002 | 1/0 | 4122 | 9 | 2 | 3 | 0 | 2 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0001c0001t0003 | 0/0 | 4122 | 11 | 9 | 2 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0001c0001t0004 | 0/0 | 4122 | 6 | 0 | 1 | 3 | 1 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0001c0002t0001 | 0/0 | 4122 | 20 | 6 | 8 | 4 | 1 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0001c0002t0007 | 0/0 | 4122 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0001c0006t0001 | 0/0 | 4122 | 6 | 6 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0001c0007t0001 | 0/1 | 4122 | 4 | 0 | 3 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0001c0010t0001 | 0/0 | 4122 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0001c0011t0001 | 0/0 | 4122 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0001c0013t0001 | 0/0 | 4122 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0001c0015t0001 | 0/0 | 4122 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0001c0018t0001 | 0/0 | 4122 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0001c0019t0001 | 0/0 | 4122 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0002c0003t0002 | 0/0 | 4122 | 9 | 3 | 4 | 0 | 0 | 2 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0002c0003t0005 | 0/0 | 4122 | 4 | 0 | 2 | 0 | 2 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0002c0004t0002 | 0/0 | 4122 | 6 | 5 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0002c0004t0006 | 0/0 | 4122 | 2 | 1 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0002c0005t0002 | 0/0 | 4122 | 4 | 4 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0002c0005t0003 | 0/0 | 4122 | 2 | 2 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0002c0005t0008 | 0/0 | 4122 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0002c0008t0006 | 0/0 | 4122 | 2 | 2 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0002c0014t0002 | 0/0 | 4122 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0003c0020t0001 | 0/0 | 4122 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0004c0009t0001 | 0/0 | 4122 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0005c0017t0001 | 0/0 | 4122 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0006c0012t0002 | 0/0 | 4122 | 1 | 0 | 0 | 0 | 1 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| a0007c0016t0001 | 0/0 | 4122 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | copy fasta | chr9 | 113458727 | 113602738 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0002g0059 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0004g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0004g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0004g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0004g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0004g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0001t0004g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0002t0007g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0006t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0006t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0006t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0006t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0006t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0006t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0007t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0007t0001g0087 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0007t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0007t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0010t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0011t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0013t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0015t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0018t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0001c0019t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0002c0003t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0002c0003t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0002c0003t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0002c0003t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0002c0003t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0002c0003t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0002c0003t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0002c0003t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0002c0003t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0002c0003t0005g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0002c0003t0005g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0002c0003t0005g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0002c0003t0005g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0002c0004t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0002c0004t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0002c0004t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0002c0004t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0002c0004t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0002c0004t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0002c0004t0006g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0002c0004t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0002c0005t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0002c0005t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0002c0005t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0002c0005t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0002c0005t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0002c0005t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0002c0005t0008g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0002c0008t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0002c0008t0006g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0002c0014t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0003c0020t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0004c0009t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0005c0017t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0006c0012t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| a0007c0016t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0006 | c0012 | t0002 | g0016 | EUR | GBR | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0079 | EUR | GBR | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | CHS | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0138 | AMR | PUR | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG00738 | hp1 | a0002 | c0003 | t0005 | g0021 | AMR | PUR | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG00738 | hp2 | a0001 | c0007 | t0001 | g0114 | AMR | PUR | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG00741 | hp1 | a0002 | c0003 | t0002 | g0075 | AMR | PUR | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01070 | hp1 | a0001 | c0007 | t0001 | g0081 | AMR | PUR | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0157 | AMR | PUR | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0051 | AMR | PUR | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0035 | AMR | PUR | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01099 | hp2 | a0002 | c0003 | t0002 | g0031 | AMR | PUR | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01106 | hp2 | a0002 | c0003 | t0002 | g0076 | AMR | PUR | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0147 | AMR | PUR | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0068 | AMR | PUR | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01167 | hp2 | a0002 | c0003 | t0005 | g0022 | AMR | PUR | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01168 | hp1 | a0001 | c0007 | t0001 | g0115 | AMR | PUR | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01168 | hp2 | a0002 | c0003 | t0002 | g0074 | AMR | PUR | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01243 | hp1 | a0002 | c0004 | t0002 | g0096 | AMR | PUR | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01243 | hp2 | a0001 | c0010 | t0001 | g0165 | AMR | PUR | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0106 | AMR | CLM | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0037 | EUR | IBS | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01516 | hp2 | a0002 | c0003 | t0005 | g0019 | EUR | IBS | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | IBS | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01517 | hp2 | a0002 | c0003 | t0005 | g0020 | EUR | IBS | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01884 | hp1 | a0007 | c0016 | t0001 | g0109 | AFR | ACB | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01884 | hp2 | a0002 | c0003 | t0002 | g0078 | AFR | ACB | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0160 | AMR | PEL | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01978 | hp2 | a0002 | c0004 | t0006 | g0018 | AMR | PEL | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | KHV | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02055 | hp1 | a0001 | c0018 | t0001 | g0139 | AFR | ACB | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | ACB | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | KHV | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02145 | hp1 | a0002 | c0003 | t0002 | g0077 | AFR | ACB | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0053 | AMR | PEL | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PEL | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02280 | hp1 | a0002 | c0005 | t0002 | g0012 | AFR | ACB | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0146 | AFR | ACB | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02572 | hp1 | a0001 | c0006 | t0001 | g0089 | AFR | GWD | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02572 | hp2 | a0002 | c0004 | t0002 | g0094 | AFR | GWD | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02698 | hp2 | a0001 | c0019 | t0001 | g0092 | SAS | PJL | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | GWD | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02723 | hp1 | a0001 | c0006 | t0001 | g0055 | AFR | GWD | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | GWD | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | GWD | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02809 | hp2 | a0002 | c0014 | t0002 | g0148 | AFR | GWD | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02818 | hp2 | a0002 | c0005 | t0008 | g0015 | AFR | GWD | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02886 | hp1 | a0001 | c0006 | t0001 | g0041 | AFR | GWD | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0046 | AFR | GWD | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0093 | AFR | GWD | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02896 | hp1 | a0002 | c0003 | t0002 | g0030 | AFR | GWD | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02896 | hp2 | a0001 | c0006 | t0001 | g0052 | AFR | GWD | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02922 | hp2 | a0002 | c0008 | t0006 | g0033 | AFR | ESN | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02970 | hp2 | a0002 | c0005 | t0003 | g0011 | AFR | ESN | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02976 | hp1 | a0001 | c0006 | t0001 | g0028 | AFR | ESN | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG03017 | hp1 | a0002 | c0003 | t0002 | g0032 | SAS | PJL | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG03041 | hp1 | a0002 | c0005 | t0003 | g0010 | AFR | GWD | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0069 | AFR | GWD | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG03098 | hp1 | a0002 | c0005 | t0002 | g0013 | AFR | MSL | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | MSL | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG03130 | hp1 | a0001 | c0011 | t0001 | g0071 | AFR | ESN | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0112 | AFR | ESN | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0113 | AFR | ESN | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG03139 | hp2 | a0002 | c0005 | t0002 | g0009 | AFR | ESN | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | MSL | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0025 | SAS | PJL | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0001 | SAS | PJL | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG03516 | hp1 | a0002 | c0004 | t0002 | g0095 | AFR | ESN | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG03540 | hp1 | a0003 | c0020 | t0001 | g0048 | AFR | GWD | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG03540 | hp2 | a0002 | c0004 | t0006 | g0023 | AFR | GWD | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | MSL | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG03831 | hp2 | a0001 | c0013 | t0001 | g0142 | SAS | BEB | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG03834 | hp1 | a0005 | c0017 | t0001 | g0083 | SAS | BEB | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | STU | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | STU | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | STU | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG04228 | hp1 | a0002 | c0003 | t0002 | g0029 | SAS | STU | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | STU | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | YRI | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA18522 | hp2 | a0002 | c0005 | t0002 | g0014 | AFR | YRI | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHB | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHB | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA18906 | hp1 | a0002 | c0004 | t0002 | g0098 | AFR | YRI | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0066 | AFR | YRI | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA18957 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA18959 | hp1 | a0004 | c0009 | t0001 | g0121 | EAS | JPT | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA18994 | hp1 | a0001 | c0002 | t0007 | g0164 | EAS | JPT | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | LWK | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA19030 | hp2 | a0001 | c0015 | t0001 | g0136 | AFR | LWK | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0056 | AFR | YRI | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | YRI | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA20129 | hp1 | a0002 | c0004 | t0002 | g0073 | AFR | ASW | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA20129 | hp2 | a0002 | c0008 | t0006 | g0034 | AFR | ASW | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0006 | EUR | TSI | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0036 | EUR | TSI | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0103 | AMR | CLM | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | CLM | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02109 | hp1 | a0001 | c0006 | t0001 | g0063 | AFR | ACB | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0125 | AFR | ACB | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0040 | AFR | ACB | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | USA | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| HG06807 | hp2 | a0002 | c0004 | t0002 | g0097 | AFR | USA | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0007 | t0001 | g0087 | REF | REF | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0059 | REF | REF | RGS3_chr9_113458727_113602738 | RGS3 | chr9 | 113458727 | 113602738 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:113507433
|
C | G | 1 | a0003 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.896C>G | p.Thr299Ser | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 11/23 | 972/4122 | 896/3261 | 299/1086 | chr9 | 113507433 | ||
| chr9:113507480
|
G | A | 1 | a0004 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.943G>A | p.Val315Ile | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 11/23 | 1019/4122 | 943/3261 | 315/1086 | chr9 | 113507480 | ||
| chr9:113583688
|
C | T | 1 | a0005 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.1940C>T | p.Pro647Leu | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/23 | 2016/4122 | 1940/3261 | 647/1086 | chr9 | 113583688 | ||
| chr9:113583838
|
G | A | 2 | a0002a0006 | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
missense_variant | MODERATE | c.2090G>A | p.Arg697Gln | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/23 | 2166/4122 | 2090/3261 | 697/1086 | chr9 | 113583838 | ||
| chr9:113584371
|
G | A | 1 | a0006 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.2623G>A | p.Gly875Ser | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/23 | 2699/4122 | 2623/3261 | 875/1086 | chr9 | 113584371 | ||
| chr9:113596825
|
C | T | 1 | a0007 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.3133C>T | p.Arg1045Trp | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 23/23 | 3209/4122 | 3133/3261 | 1045/1086 | chr9 | 113596825 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:113463817
|
G | A | 1 | a0002c0008 | 2 | HG02922.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.15G>A | p.Leu5Leu | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/23 | 91/4122 | 15/3261 | 5/1086 | chr9 | 113463817 | ||
| chr9:113507612
|
C | T | 2 | a0001c0018a0001c0019 | 2 | HG02055.hp1 HG02698.hp2 |
synonymous_variant | LOW | c.1075C>T | p.Leu359Leu | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 11/23 | 1151/4122 | 1075/3261 | 359/1086 | chr9 | 113507612 | ||
| chr9:113514567
|
G | A | 1 | a0001c0010 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.1251G>A | p.Pro417Pro | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 13/23 | 1327/4122 | 1251/3261 | 417/1086 | chr9 | 113514567 | ||
| chr9:113517600
|
T | C | 6 | a0001c0011a0002c0003a0002c0004others(3): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
synonymous_variant | LOW | c.1398T>C | p.Tyr466Tyr | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/23 | 1474/4122 | 1398/3261 | 466/1086 | chr9 | 113517600 | ||
| chr9:113517606
|
G | A | 1 | a0001c0018 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.1404G>A | p.Gly468Gly | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/23 | 1480/4122 | 1404/3261 | 468/1086 | chr9 | 113517606 | ||
| chr9:113522932
|
G | A | 1 | a0001c0011 | 1 | HG03130.hp1 | splice_region_variant&synonymous_variant | LOW | c.1425G>A | p.Val475Val | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/23 | 1501/4122 | 1425/3261 | 475/1086 | chr9 | 113522932 | ||
| chr9:113529234
|
C | T | 2 | a0001c0007a0005c0017 | 5 | HG00738.hp2 HG01070.hp1 HG01168.hp1 others(2): Show |
synonymous_variant | LOW | c.1548C>T | p.Asp516Asp | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/23 | 1624/4122 | 1548/3261 | 516/1086 | chr9 | 113529234 | ||
| chr9:113583689
|
G | A | 1 | a0001c0013 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.1941G>A | p.Pro647Pro | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/23 | 2017/4122 | 1941/3261 | 647/1086 | chr9 | 113583689 | ||
| chr9:113583956
|
G | A | 6 | a0002c0003a0002c0004a0002c0005others(3): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
synonymous_variant | LOW | c.2208G>A | p.Ala736Ala | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/23 | 2284/4122 | 2208/3261 | 736/1086 | chr9 | 113583956 | ||
| chr9:113583992
|
G | A | 1 | a0001c0015 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.2244G>A | p.Arg748Arg | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/23 | 2320/4122 | 2244/3261 | 748/1086 | chr9 | 113583992 | ||
| chr9:113584007
|
C | T | 2 | a0001c0002a0001c0010 | 22 | HG00140.hp2 HG00408.hp1 HG00735.hp2 others(19): Show |
synonymous_variant | LOW | c.2259C>T | p.Tyr753Tyr | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/23 | 2335/4122 | 2259/3261 | 753/1086 | chr9 | 113584007 | ||
| chr9:113584235
|
G | A | 1 | a0002c0005 | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
synonymous_variant | LOW | c.2487G>A | p.Thr829Thr | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/23 | 2563/4122 | 2487/3261 | 829/1086 | chr9 | 113584235 | ||
| chr9:113591338
|
C | T | 1 | a0001c0006 | 6 | HG02109.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
synonymous_variant | LOW | c.2685C>T | p.Ser895Ser | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 19/23 | 2761/4122 | 2685/3261 | 895/1086 | chr9 | 113591338 | ||
| chr9:113594496
|
C | T | 2 | a0002c0003a0006c0012 | 14 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(11): Show |
synonymous_variant | LOW | c.2811C>T | p.Pro937Pro | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 20/23 | 2887/4122 | 2811/3261 | 937/1086 | chr9 | 113594496 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:113596990
|
G | A | 1 | a0001c0001t0004 | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*37G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 23/23 | 37 | chr9 | 113596990 | |||||
| chr9:113596992
|
G | A | 1 | a0001c0002t0007 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*39G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 23/23 | 39 | chr9 | 113596992 | |||||
| chr9:113597059
|
T | C | 18 | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(15): Show | 127 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*106T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 23/23 | 106 | chr9 | 113597059 | |||||
| chr9:113597132
|
T | G | 2 | a0002c0004t0006a0002c0008t0006 | 4 | HG01978.hp2 HG02922.hp2 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*179T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 23/23 | 179 | chr9 | 113597132 | |||||
| chr9:113597172
|
G | A | 1 | a0002c0005t0008 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*219G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 23/23 | 219 | chr9 | 113597172 | |||||
| chr9:113597263
|
G | A | 2 | a0001c0001t0003a0002c0005t0003 | 13 | HG01081.hp1 HG01109.hp2 HG02055.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*310G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 23/23 | 310 | chr9 | 113597263 | |||||
| chr9:113597300
|
G | C | 1 | a0002c0003t0005 | 4 | HG00738.hp1 HG01167.hp2 HG01516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*347G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 23/23 | 347 | chr9 | 113597300 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:113463948
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.79+67C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113463948 | ||||||
| chr9:113464037
|
G | A | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+156G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113464037 | ||||||
| chr9:113464472
|
G | A | 2 | a0001c0001t0001g0008a0001c0002t0001g0007 | 2 | HG02040.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.79+591G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113464472 | ||||||
| chr9:113465081
|
G | GTT | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+1203_79+1204dup others(2): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 113465081 | |||||
| chr9:113465109
|
C | T | 1 | a0001c0001t0004g0006 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.79+1228C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113465109 | ||||||
| chr9:113465339
|
G | A | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+1458G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113465339 | ||||||
| chr9:113465439
|
C | CTG | 20 | a0001c0001t0001g0072a0001c0001t0001g0080a0001c0001t0001g0082others(17): Show | 20 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.79+1599_79+1600dup others(2): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 113465439 | |||||
| chr9:113465439
|
C | CTGTG | 54 | a0001c0001t0001g0008a0001c0001t0001g0099a0001c0001t0001g0100others(51): Show | 54 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.79+1597_79+1600dup others(4): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 113465439 | |||||
| chr9:113465439
|
C | CTGTGTG | 15 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0143others(12): Show | 15 | HG00639.hp2 HG01106.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.79+1595_79+1600dup others(6): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 113465439 | |||||
| chr9:113465439
|
C | CTGTGTGT others(1): Show |
15 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(12): Show | 15 | HG00544.hp1 HG00558.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.79+1593_79+1600dup others(8): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 113465439 | |||||
| chr9:113465439
|
C | CTGTGTGT others(3): Show |
2 | a0001c0001t0001g0166a0001c0010t0001g0165 | 2 | HG01243.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.79+1591_79+1600dup others(10): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 113465439 | |||||
| chr9:113465439
|
C | CTGTGTGT others(11): Show |
1 | a0001c0001t0001g0167 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.79+1583_79+1600dup others(18): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 113465439 | |||||
| chr9:113465439
|
CTG | C | 10 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0003g0026others(7): Show | 10 | HG00738.hp1 HG01167.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+1599_79+1600del others(2): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 113465439 | |||||
| chr9:113465439
|
CTGTG | C | 2 | a0001c0001t0001g0017a0006c0012t0002g0016 | 2 | HG00140.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.79+1597_79+1600del others(4): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 113465439 | |||||
| chr9:113465476
|
T | TGTGTGC | 4 | a0001c0001t0004g0002a0001c0001t0004g0003a0001c0001t0004g0004others(1): Show | 4 | HG02132.hp1 HG02148.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+1596_79+1601dup others(6): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 113465476 | |||||
| chr9:113465545
|
T | C | 1 | a0001c0001t0001g0072 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.79+1664T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113465545 | ||||||
| chr9:113465783
|
G | C | 2 | a0001c0018t0001g0139a0001c0019t0001g0092 | 2 | HG02055.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.79+1902G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113465783 | ||||||
| chr9:113466167
|
G | A | 1 | a0001c0002t0001g0093 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.79+2286G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113466167 | ||||||
| chr9:113466221
|
G | A | 1 | a0002c0004t0006g0018 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.79+2340G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113466221 | ||||||
| chr9:113466477
|
T | G | 1 | a0001c0006t0001g0028 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.79+2596T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113466477 | ||||||
| chr9:113466645
|
G | A | 31 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(28): Show | 31 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.79+2764G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113466645 | ||||||
| chr9:113467027
|
C | T | 2 | a0002c0008t0006g0033a0002c0008t0006g0034 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.79+3146C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113467027 | ||||||
| chr9:113467051
|
CCATT | C | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+3175_79+3178del others(4): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 113467051 | |||||
| chr9:113467063
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.79+3182A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113467063 | ||||||
| chr9:113467189
|
A | T | 1 | a0001c0018t0001g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.79+3308A>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113467189 | ||||||
| chr9:113467296
|
G | A | 6 | a0001c0001t0001g0072a0001c0001t0001g0099a0001c0001t0001g0100others(3): Show | 6 | HG00408.hp2 HG00621.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+3415G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113467296 | ||||||
| chr9:113467406
|
T | C | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | NA18962.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.79+3525T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113467406 | ||||||
| chr9:113467458
|
G | A | 1 | a0001c0002t0001g0079 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.79+3577G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113467458 | ||||||
| chr9:113467770
|
A | G | 8 | a0001c0011t0001g0071a0002c0005t0002g0009a0002c0005t0002g0012others(5): Show | 8 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.79+3889A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113467770 | ||||||
| chr9:113468075
|
T | C | 8 | a0001c0018t0001g0139a0001c0019t0001g0092a0002c0004t0002g0073others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.79+4194T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113468075 | ||||||
| chr9:113468151
|
C | A | 1 | a0001c0001t0001g0080 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.79+4270C>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113468151 | ||||||
| chr9:113468752
|
G | T | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+4871G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113468752 | ||||||
| chr9:113468940
|
G | C | 14 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(11): Show | 14 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.79+5059G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113468940 | ||||||
| chr9:113468944
|
G | A | 3 | a0001c0001t0001g0104a0001c0002t0001g0035a0001c0002t0001g0103 | 3 | HG01099.hp1 HG01123.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.79+5063G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113468944 | ||||||
| chr9:113469042
|
A | AT | 19 | a0001c0001t0001g0065a0001c0001t0001g0090a0001c0001t0001g0091others(16): Show | 19 | HG00408.hp1 HG00621.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.79+5183dupT | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 113469042 | |||||
| chr9:113469042
|
AT | A | 9 | a0001c0002t0001g0093a0001c0010t0001g0165a0002c0003t0002g0074others(6): Show | 9 | HG01168.hp2 HG01243.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.79+5183delT | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 113469042 | |||||
| chr9:113469165
|
T | C | 4 | a0002c0004t0006g0018a0002c0004t0006g0023a0002c0008t0006g0033others(1): Show | 4 | HG01978.hp2 HG02922.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+5284T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113469165 | ||||||
| chr9:113469210
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.79+5329G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113469210 | ||||||
| chr9:113469226
|
G | A | 31 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(28): Show | 31 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.79+5345G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113469226 | ||||||
| chr9:113469672
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.79+5791A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113469672 | ||||||
| chr9:113469704
|
A | T | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+5823A>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113469704 | ||||||
| chr9:113469900
|
G | GT | 25 | a0001c0001t0001g0027a0001c0001t0001g0064a0001c0001t0001g0080others(22): Show | 25 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.79+6034dupT | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 113469900 | |||||
| chr9:113469918
|
C | T | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+6037C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113469918 | ||||||
| chr9:113469962
|
G | A | 2 | a0001c0001t0002g0036a0001c0001t0002g0037 | 2 | HG01516.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.79+6081G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113469962 | ||||||
| chr9:113469980
|
A | G | 2 | a0002c0004t0006g0018a0002c0004t0006g0023 | 2 | HG01978.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.79+6099A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113469980 | ||||||
| chr9:113470092
|
G | A | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+6211G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113470092 | ||||||
| chr9:113470131
|
G | C | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.79+6250G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113470131 | ||||||
| chr9:113470172
|
A | AAG | 161 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0024others(158): Show | 161 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.79+6294_79+6295dup others(2): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 113470172 | |||||
| chr9:113470337
|
G | A | 31 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(28): Show | 31 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.79+6456G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113470337 | ||||||
| chr9:113470342
|
G | A | 2 | a0002c0005t0002g0009a0002c0005t0002g0012 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.79+6461G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113470342 | ||||||
| chr9:113470725
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.79+6844G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113470725 | ||||||
| chr9:113470829
|
A | T | 6 | a0001c0001t0001g0072a0001c0001t0001g0099a0001c0001t0001g0100others(3): Show | 6 | HG00408.hp2 HG00621.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+6948A>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113470829 | ||||||
| chr9:113470897
|
C | G | 1 | a0001c0002t0001g0160 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.79+7016C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113470897 | ||||||
| chr9:113471333
|
A | G | 2 | a0001c0001t0001g0163a0002c0008t0006g0034 | 2 | NA18997.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.79+7452A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113471333 | ||||||
| chr9:113471715
|
C | G | 1 | a0001c0001t0003g0056 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.80-7776C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113471715 | ||||||
| chr9:113471910
|
T | G | 6 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(3): Show | 6 | HG01243.hp1 HG02572.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-7581T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113471910 | ||||||
| chr9:113471968
|
G | T | 1 | a0001c0001t0001g0159 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.80-7523G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113471968 | ||||||
| chr9:113472024
|
G | A | 33 | a0001c0018t0001g0139a0001c0019t0001g0092a0002c0003t0002g0029others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.80-7467G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113472024 | ||||||
| chr9:113472032
|
T | A | 33 | a0001c0018t0001g0139a0001c0019t0001g0092a0002c0003t0002g0029others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.80-7459T>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113472032 | ||||||
| chr9:113472090
|
T | C | 2 | a0001c0018t0001g0139a0001c0019t0001g0092 | 2 | HG02055.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.80-7401T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113472090 | ||||||
| chr9:113472096
|
T | C | 2 | a0001c0001t0001g0107a0001c0002t0001g0106 | 2 | HG01258.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.80-7395T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113472096 | ||||||
| chr9:113472307
|
G | A | 33 | a0001c0018t0001g0139a0001c0019t0001g0092a0002c0003t0002g0029others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.80-7184G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113472307 | ||||||
| chr9:113472331
|
C | T | 2 | a0002c0004t0006g0018a0002c0004t0006g0023 | 2 | HG01978.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.80-7160C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113472331 | ||||||
| chr9:113472957
|
T | G | 6 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(3): Show | 6 | HG01243.hp1 HG02572.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-6534T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113472957 | ||||||
| chr9:113474037
|
A | G | 1 | a0001c0001t0001g0158 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.80-5454A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113474037 | ||||||
| chr9:113474052
|
T | G | 1 | a0001c0002t0001g0160 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.80-5439T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113474052 | ||||||
| chr9:113474081
|
A | AC | 34 | a0001c0011t0001g0071a0001c0018t0001g0139a0001c0019t0001g0092others(31): Show | 34 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.80-5409dupC | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 113474081 | |||||
| chr9:113474152
|
G | A | 40 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(37): Show | 40 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.80-5339G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113474152 | ||||||
| chr9:113474326
|
G | A | 1 | a0001c0001t0003g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.80-5165G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113474326 | ||||||
| chr9:113474517
|
A | G | 6 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(3): Show | 6 | HG01243.hp1 HG02572.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-4974A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113474517 | ||||||
| chr9:113474562
|
A | G | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.80-4929A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113474562 | ||||||
| chr9:113474605
|
A | C | 2 | a0002c0003t0002g0077a0002c0003t0002g0078 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.80-4886A>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113474605 | ||||||
| chr9:113474610
|
C | T | 38 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(35): Show | 38 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.80-4881C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113474610 | ||||||
| chr9:113474906
|
T | C | 18 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(15): Show | 18 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.80-4585T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113474906 | ||||||
| chr9:113474911
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.80-4580T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113474911 | ||||||
| chr9:113474936
|
G | A | 2 | a0001c0001t0001g0108a0007c0016t0001g0109 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.80-4555G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113474936 | ||||||
| chr9:113475065
|
A | G | 1 | a0001c0006t0001g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.80-4426A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113475065 | ||||||
| chr9:113475109
|
A | G | 3 | a0002c0004t0002g0073a0002c0004t0002g0097a0002c0004t0002g0098 | 3 | HG06807.hp2 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.80-4382A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113475109 | ||||||
| chr9:113475448
|
C | T | 1 | a0001c0001t0001g0072 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.80-4043C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113475448 | ||||||
| chr9:113475559
|
C | T | 1 | a0002c0014t0002g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.80-3932C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113475559 | ||||||
| chr9:113475707
|
A | G | 6 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(3): Show | 6 | HG01243.hp1 HG02572.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-3784A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113475707 | ||||||
| chr9:113475963
|
G | A | 1 | a0001c0007t0001g0081 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.80-3528G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113475963 | ||||||
| chr9:113476016
|
T | C | 38 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(35): Show | 38 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.80-3475T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113476016 | ||||||
| chr9:113476105
|
C | A | 2 | a0002c0004t0006g0018a0002c0004t0006g0023 | 2 | HG01978.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.80-3386C>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113476105 | ||||||
| chr9:113476143
|
G | T | 2 | a0002c0008t0006g0033a0002c0008t0006g0034 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.80-3348G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113476143 | ||||||
| chr9:113476190
|
A | G | 2 | a0001c0007t0001g0081a0001c0007t0001g0087 | 2 | HG01070.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.80-3301A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113476190 | ||||||
| chr9:113476218
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.80-3273G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113476218 | ||||||
| chr9:113476274
|
G | C | 2 | a0001c0001t0001g0110a0001c0001t0001g0141 | 2 | HG01981.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.80-3217G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113476274 | ||||||
| chr9:113476739
|
G | C | 1 | a0001c0001t0001g0088 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.80-2752G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113476739 | ||||||
| chr9:113476925
|
C | G | 1 | a0001c0001t0001g0027 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.80-2566C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113476925 | ||||||
| chr9:113476989
|
G | A | 1 | a0001c0001t0004g0006 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.80-2502G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113476989 | ||||||
| chr9:113477067
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.80-2424C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113477067 | ||||||
| chr9:113477218
|
TA | T | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-2271delA | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr9 | 113477218 | |||||
| chr9:113477414
|
T | C | 1 | a0001c0002t0001g0040 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.80-2077T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113477414 | ||||||
| chr9:113477581
|
A | G | 1 | a0001c0001t0001g0133 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.80-1910A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113477581 | ||||||
| chr9:113477696
|
T | G | 8 | a0001c0018t0001g0139a0001c0019t0001g0092a0002c0004t0002g0073others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.80-1795T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113477696 | ||||||
| chr9:113477761
|
G | A | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-1730G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113477761 | ||||||
| chr9:113477794
|
C | T | 1 | a0002c0008t0006g0033 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.80-1697C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113477794 | ||||||
| chr9:113477965
|
A | G | 34 | a0001c0011t0001g0071a0001c0018t0001g0139a0001c0019t0001g0092others(31): Show | 34 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.80-1526A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113477965 | ||||||
| chr9:113478145
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.80-1346C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113478145 | ||||||
| chr9:113478162
|
C | T | 2 | a0002c0003t0002g0077a0002c0003t0002g0078 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.80-1329C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113478162 | ||||||
| chr9:113478201
|
C | T | 21 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(18): Show | 21 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.80-1290C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113478201 | ||||||
| chr9:113478336
|
A | T | 1 | a0001c0001t0004g0001 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.80-1155A>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113478336 | ||||||
| chr9:113478524
|
C | T | 1 | a0001c0002t0001g0053 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.80-967C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113478524 | ||||||
| chr9:113478542
|
C | A | 6 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(3): Show | 6 | HG01243.hp1 HG02572.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-949C>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113478542 | ||||||
| chr9:113478551
|
G | A | 6 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(3): Show | 6 | HG01243.hp1 HG02572.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-940G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113478551 | ||||||
| chr9:113478612
|
C | A | 2 | a0002c0003t0002g0077a0002c0003t0002g0078 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.80-879C>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113478612 | ||||||
| chr9:113478691
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.80-800A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113478691 | ||||||
| chr9:113478794
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.80-697A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113478794 | ||||||
| chr9:113478957
|
G | A | 15 | a0001c0001t0001g0017a0001c0001t0001g0151a0001c0001t0001g0152others(12): Show | 15 | HG00544.hp1 HG00558.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.80-534G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113478957 | ||||||
| chr9:113479188
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.80-303A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113479188 | ||||||
| chr9:113479309
|
C | T | 1 | a0001c0006t0001g0052 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.80-182C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113479309 | ||||||
| chr9:113479414
|
G | A | 1 | a0002c0004t0002g0094 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.80-77G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113479414 | ||||||
| chr9:113479427
|
T | C | 34 | a0001c0011t0001g0071a0001c0018t0001g0139a0001c0019t0001g0092others(31): Show | 34 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.80-64T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 1/22 | chr9 | 113479427 | ||||||
| chr9:113479657
|
G | A | 14 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(11): Show | 14 | HG00544.hp1 HG00558.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.130+116G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 2/22 | chr9 | 113479657 | ||||||
| chr9:113479736
|
A | G | 1 | a0001c0010t0001g0165 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.130+195A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 2/22 | chr9 | 113479736 | ||||||
| chr9:113479900
|
A | T | 1 | a0002c0003t0002g0032 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.130+359A>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 2/22 | chr9 | 113479900 | ||||||
| chr9:113479996
|
G | A | 2 | a0001c0001t0001g0107a0001c0002t0001g0106 | 2 | HG01258.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.130+455G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 2/22 | chr9 | 113479996 | ||||||
| chr9:113480026
|
C | T | 4 | a0002c0005t0002g0013a0002c0005t0002g0014a0002c0005t0003g0010others(1): Show | 4 | HG02970.hp2 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+485C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 2/22 | chr9 | 113480026 | ||||||
| chr9:113480242
|
C | A | 34 | a0001c0011t0001g0071a0001c0018t0001g0139a0001c0019t0001g0092others(31): Show | 34 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.130+701C>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 2/22 | chr9 | 113480242 | ||||||
| chr9:113480261
|
G | A | 63 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0151others(60): Show | 63 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.130+720G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 2/22 | chr9 | 113480261 | ||||||
| chr9:113480453
|
C | T | 1 | a0001c0011t0001g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.130+912C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 2/22 | chr9 | 113480453 | ||||||
| chr9:113480458
|
C | CA | 9 | a0001c0001t0001g0091a0001c0001t0001g0111a0001c0001t0004g0001others(6): Show | 9 | HG01243.hp1 HG02132.hp1 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.130+937dupA | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 113480458 | |||||
| chr9:113480458
|
C | CAA | 11 | a0001c0011t0001g0071a0001c0018t0001g0139a0001c0019t0001g0092others(8): Show | 11 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.130+936_130+937dup others(2): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 113480458 | |||||
| chr9:113480458
|
C | CAAA | 15 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(12): Show | 15 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.130+935_130+937dup others(3): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 113480458 | |||||
| chr9:113480607
|
G | T | 2 | a0001c0001t0003g0026a0001c0002t0001g0051 | 2 | HG01081.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.130+1066G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 2/22 | chr9 | 113480607 | ||||||
| chr9:113480664
|
C | G | 1 | a0002c0003t0005g0022 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.130+1123C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 2/22 | chr9 | 113480664 | ||||||
| chr9:113480912
|
C | G | 2 | a0002c0004t0006g0018a0002c0004t0006g0023 | 2 | HG01978.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.130+1371C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 2/22 | chr9 | 113480912 | ||||||
| chr9:113481131
|
A | G | 1 | a0001c0001t0001g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.130+1590A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 2/22 | chr9 | 113481131 | ||||||
| chr9:113481135
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.130+1594T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 2/22 | chr9 | 113481135 | ||||||
| chr9:113481325
|
G | C | 34 | a0001c0011t0001g0071a0001c0018t0001g0139a0001c0019t0001g0092others(31): Show | 34 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.131-1734G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 2/22 | chr9 | 113481325 | ||||||
| chr9:113481771
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.131-1288G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 2/22 | chr9 | 113481771 | ||||||
| chr9:113482046
|
C | CA | 6 | a0001c0001t0001g0082a0001c0001t0001g0111a0001c0002t0001g0112others(3): Show | 6 | HG01978.hp1 HG02109.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.131-999dupA | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 113482046 | |||||
| chr9:113482046
|
CA | C | 20 | a0001c0018t0001g0139a0001c0019t0001g0092a0002c0003t0002g0029others(17): Show | 20 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.131-999delA | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 113482046 | |||||
| chr9:113482454
|
G | C | 5 | a0001c0001t0001g0065a0001c0001t0002g0067a0001c0001t0003g0066others(2): Show | 5 | HG01109.hp2 HG02723.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.131-605G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 2/22 | chr9 | 113482454 | ||||||
| chr9:113482620
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.131-439G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 2/22 | chr9 | 113482620 | ||||||
| chr9:113482702
|
T | C | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.131-357T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 2/22 | chr9 | 113482702 | ||||||
| chr9:113482965
|
G | A | 1 | a0002c0004t0002g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.131-94G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 2/22 | chr9 | 113482965 | ||||||
| chr9:113483002
|
G | A | 6 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(3): Show | 6 | HG01243.hp1 HG02572.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.131-57G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 2/22 | chr9 | 113483002 | ||||||
| chr9:113483343
|
C | T | 1 | a0001c0001t0004g0004 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.189+226C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 3/22 | chr9 | 113483343 | ||||||
| chr9:113483775
|
G | A | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-363G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 3/22 | chr9 | 113483775 | ||||||
| chr9:113484255
|
C | G | 34 | a0001c0011t0001g0071a0001c0018t0001g0139a0001c0019t0001g0092others(31): Show | 34 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.284+23C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 4/22 | chr9 | 113484255 | ||||||
| chr9:113484309
|
T | A | 7 | a0001c0011t0001g0071a0002c0004t0002g0073a0002c0004t0002g0094others(4): Show | 7 | HG01243.hp1 HG02572.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.284+77T>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 4/22 | chr9 | 113484309 | ||||||
| chr9:113484327
|
C | CA | 30 | a0001c0001t0001g0042a0001c0001t0001g0105a0001c0001t0001g0108others(27): Show | 30 | HG00140.hp2 HG00738.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.284+117dupA | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr9 | 113484327 | |||||
| chr9:113484327
|
C | CAA | 5 | a0002c0004t0002g0073a0002c0004t0002g0096a0002c0004t0002g0097others(2): Show | 5 | HG01243.hp1 HG02970.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.284+116_284+117dup others(2): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr9 | 113484327 | |||||
| chr9:113484327
|
CA | C | 17 | a0001c0001t0001g0082a0001c0001t0001g0086a0001c0001t0001g0088others(14): Show | 17 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.284+117delA | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr9 | 113484327 | |||||
| chr9:113484330
|
AAAAAAAA others(19): Show |
A | 18 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(15): Show | 18 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.284+107_284+132del others(26): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr9 | 113484330 | |||||
| chr9:113484374
|
T | C | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.284+142T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 4/22 | chr9 | 113484374 | ||||||
| chr9:113484412
|
T | C | 19 | a0001c0002t0001g0103a0002c0003t0002g0029a0002c0003t0002g0030others(16): Show | 19 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.284+180T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 4/22 | chr9 | 113484412 | ||||||
| chr9:113484430
|
G | T | 1 | a0001c0011t0001g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.284+198G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 4/22 | chr9 | 113484430 | ||||||
| chr9:113484605
|
T | C | 40 | a0001c0006t0001g0028a0001c0006t0001g0041a0001c0006t0001g0052others(37): Show | 40 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.284+373T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 4/22 | chr9 | 113484605 | ||||||
| chr9:113485094
|
A | AT | 130 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0024others(127): Show | 130 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.285-520dupT | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr9 | 113485094 | |||||
| chr9:113485094
|
A | ATT | 6 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(3): Show | 6 | HG01243.hp1 HG02572.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-521_285-520dup others(2): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr9 | 113485094 | |||||
| chr9:113485240
|
G | A | 2 | a0001c0001t0001g0047a0003c0020t0001g0048 | 2 | HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.285-385G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 4/22 | chr9 | 113485240 | ||||||
| chr9:113485714
|
G | A | 2 | a0001c0018t0001g0139a0001c0019t0001g0092 | 2 | HG02055.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.353+21G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113485714 | ||||||
| chr9:113485777
|
G | A | 2 | a0001c0001t0001g0107a0001c0002t0001g0106 | 2 | HG01258.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.353+84G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113485777 | ||||||
| chr9:113485782
|
G | T | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.353+89G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113485782 | ||||||
| chr9:113486638
|
A | C | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.353+945A>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113486638 | ||||||
| chr9:113486650
|
G | A | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.353+957G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113486650 | ||||||
| chr9:113487024
|
TGTTAATA others(40): Show |
T | 2 | a0001c0018t0001g0139a0001c0019t0001g0092 | 2 | HG02055.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.353+1333_353+1379d others(49): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr9 | 113487024 | |||||
| chr9:113487100
|
C | CT | 14 | a0001c0001t0001g0080a0001c0001t0001g0082a0001c0001t0001g0085others(11): Show | 14 | HG01243.hp1 HG01884.hp2 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.353+1429dupT | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr9 | 113487100 | |||||
| chr9:113487100
|
CT | C | 15 | a0001c0001t0001g0047a0001c0001t0004g0001a0001c0006t0001g0052others(12): Show | 15 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.353+1429delT | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr9 | 113487100 | |||||
| chr9:113487198
|
G | A | 3 | a0002c0004t0002g0094a0002c0004t0002g0095a0002c0004t0002g0096 | 3 | HG01243.hp1 HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.353+1505G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113487198 | ||||||
| chr9:113487313
|
T | G | 1 | a0001c0011t0001g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.353+1620T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113487313 | ||||||
| chr9:113487354
|
AC | A | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.353+1664delC | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr9 | 113487354 | |||||
| chr9:113487493
|
A | C | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.353+1800A>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113487493 | ||||||
| chr9:113487539
|
C | T | 1 | a0001c0011t0001g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.353+1846C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113487539 | ||||||
| chr9:113487803
|
T | C | 34 | a0001c0011t0001g0071a0001c0018t0001g0139a0001c0019t0001g0092others(31): Show | 34 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.353+2110T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113487803 | ||||||
| chr9:113488538
|
G | A | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.353+2845G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113488538 | ||||||
| chr9:113488668
|
C | T | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.353+2975C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113488668 | ||||||
| chr9:113488685
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.353+2992G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113488685 | ||||||
| chr9:113488775
|
G | A | 1 | a0001c0011t0001g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.353+3082G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113488775 | ||||||
| chr9:113488851
|
C | T | 1 | a0001c0011t0001g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.353+3158C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113488851 | ||||||
| chr9:113489006
|
G | C | 1 | a0001c0001t0003g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.353+3313G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113489006 | ||||||
| chr9:113489019
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.353+3326T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113489019 | ||||||
| chr9:113489079
|
G | T | 1 | a0001c0006t0001g0041 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.353+3386G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113489079 | ||||||
| chr9:113489085
|
A | G | 34 | a0001c0011t0001g0071a0001c0018t0001g0139a0001c0019t0001g0092others(31): Show | 34 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.353+3392A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113489085 | ||||||
| chr9:113489623
|
T | A | 40 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(37): Show | 40 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.353+3930T>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113489623 | ||||||
| chr9:113489694
|
A | AT | 9 | a0001c0001t0001g0047a0001c0001t0003g0070a0001c0002t0001g0051others(6): Show | 9 | HG01081.hp2 HG01243.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.353+4017dupT | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr9 | 113489694 | |||||
| chr9:113489694
|
AT | A | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.353+4017delT | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr9 | 113489694 | |||||
| chr9:113489840
|
T | G | 1 | a0001c0006t0001g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.353+4147T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113489840 | ||||||
| chr9:113489943
|
T | C | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.353+4250T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113489943 | ||||||
| chr9:113489963
|
A | G | 19 | a0001c0001t0001g0008a0001c0001t0001g0072a0001c0001t0001g0082others(16): Show | 19 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.353+4270A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113489963 | ||||||
| chr9:113490007
|
G | A | 2 | a0001c0001t0001g0047a0003c0020t0001g0048 | 2 | HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.353+4314G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113490007 | ||||||
| chr9:113490218
|
T | C | 40 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(37): Show | 40 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.353+4525T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113490218 | ||||||
| chr9:113490268
|
G | C | 2 | a0001c0018t0001g0139a0001c0019t0001g0092 | 2 | HG02055.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.353+4575G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113490268 | ||||||
| chr9:113490404
|
T | TA | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.353+4719dupA | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr9 | 113490404 | |||||
| chr9:113490494
|
T | C | 1 | a0001c0002t0001g0035 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.353+4801T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113490494 | ||||||
| chr9:113490633
|
A | G | 6 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(3): Show | 6 | HG01243.hp1 HG02572.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.353+4940A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113490633 | ||||||
| chr9:113490646
|
T | TATATAAT others(29): Show |
29 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(26): Show | 29 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.353+4968_353+5003d others(38): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr9 | 113490646 | |||||
| chr9:113490646
|
T | TATATAAT others(65): Show |
3 | a0002c0004t0002g0094a0002c0004t0002g0095a0002c0004t0002g0096 | 3 | HG01243.hp1 HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.353+5003_353+5004i others(74): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr9 | 113490646 | |||||
| chr9:113490721
|
A | G | 14 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(11): Show | 14 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.353+5028A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113490721 | ||||||
| chr9:113490742
|
AATTAT | A | 2 | a0001c0001t0001g0108a0007c0016t0001g0109 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.354-5040_354-5036d others(7): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr9 | 113490742 | |||||
| chr9:113490768
|
A | G | 2 | a0001c0002t0001g0007a0001c0002t0001g0126 | 2 | HG02040.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.354-5018A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113490768 | ||||||
| chr9:113490779
|
A | T | 34 | a0001c0011t0001g0071a0001c0018t0001g0139a0001c0019t0001g0092others(31): Show | 34 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.354-5007A>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113490779 | ||||||
| chr9:113490794
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.354-4992G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113490794 | ||||||
| chr9:113490824
|
TTATATCA others(34): Show |
T | 3 | a0001c0001t0001g0104a0001c0002t0001g0035a0001c0002t0001g0103 | 3 | HG01099.hp1 HG01123.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.354-4873_354-4833d others(43): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr9 | 113490824 | |||||
| chr9:113490913
|
A | G | 2 | a0001c0018t0001g0139a0001c0019t0001g0092 | 2 | HG02055.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.354-4873A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113490913 | ||||||
| chr9:113490964
|
A | C | 1 | a0001c0001t0001g0156 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.354-4822A>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113490964 | ||||||
| chr9:113490976
|
TTAA | T | 3 | a0001c0001t0001g0116a0002c0008t0006g0033a0002c0008t0006g0034 | 3 | HG01517.hp1 HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.354-4808_354-4806d others(5): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr9 | 113490976 | |||||
| chr9:113491013
|
C | T | 7 | a0001c0001t0001g0116a0001c0001t0004g0001a0001c0001t0004g0002others(4): Show | 7 | HG01517.hp1 HG02132.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.354-4773C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113491013 | ||||||
| chr9:113491051
|
CTT | C | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.354-4734_354-4733d others(4): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113491051 | ||||||
| chr9:113491096
|
A | G | 2 | a0001c0002t0001g0007a0001c0002t0001g0126 | 2 | HG02040.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.354-4690A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113491096 | ||||||
| chr9:113491214
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.354-4572G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113491214 | ||||||
| chr9:113491249
|
G | A | 34 | a0001c0011t0001g0071a0001c0018t0001g0139a0001c0019t0001g0092others(31): Show | 34 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.354-4537G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113491249 | ||||||
| chr9:113491520
|
A | G | 40 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(37): Show | 40 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.354-4266A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113491520 | ||||||
| chr9:113491589
|
C | T | 4 | a0002c0005t0002g0013a0002c0005t0002g0014a0002c0005t0003g0010others(1): Show | 4 | HG02970.hp2 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.354-4197C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113491589 | ||||||
| chr9:113491591
|
G | T | 4 | a0002c0005t0002g0013a0002c0005t0002g0014a0002c0005t0003g0010others(1): Show | 4 | HG02970.hp2 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.354-4195G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113491591 | ||||||
| chr9:113491617
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.354-4169C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113491617 | ||||||
| chr9:113492000
|
C | T | 2 | a0001c0001t0001g0140a0001c0015t0001g0136 | 2 | HG00639.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.354-3786C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113492000 | ||||||
| chr9:113492188
|
T | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0049 | 2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.354-3598T>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113492188 | ||||||
| chr9:113492268
|
A | T | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.354-3518A>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113492268 | ||||||
| chr9:113492411
|
G | T | 1 | a0001c0001t0001g0017 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.354-3375G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113492411 | ||||||
| chr9:113492473
|
C | T | 2 | a0001c0001t0001g0047a0003c0020t0001g0048 | 2 | HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.354-3313C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113492473 | ||||||
| chr9:113492534
|
A | G | 102 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0024others(99): Show | 102 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.354-3252A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113492534 | ||||||
| chr9:113492568
|
T | G | 1 | a0001c0001t0001g0141 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.354-3218T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113492568 | ||||||
| chr9:113492945
|
G | A | 34 | a0001c0011t0001g0071a0001c0018t0001g0139a0001c0019t0001g0092others(31): Show | 34 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.354-2841G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113492945 | ||||||
| chr9:113493400
|
G | A | 4 | a0002c0004t0006g0018a0002c0004t0006g0023a0002c0008t0006g0033others(1): Show | 4 | HG01978.hp2 HG02922.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.354-2386G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113493400 | ||||||
| chr9:113493518
|
A | G | 2 | a0001c0018t0001g0139a0001c0019t0001g0092 | 2 | HG02055.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.354-2268A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113493518 | ||||||
| chr9:113493868
|
C | G | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.354-1918C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113493868 | ||||||
| chr9:113494109
|
A | G | 1 | a0001c0002t0001g0040 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.354-1677A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113494109 | ||||||
| chr9:113494115
|
G | C | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.354-1671G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113494115 | ||||||
| chr9:113494141
|
A | G | 1 | a0001c0010t0001g0165 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.354-1645A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113494141 | ||||||
| chr9:113494355
|
C | T | 1 | a0001c0007t0001g0087 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.354-1431C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113494355 | ||||||
| chr9:113494364
|
C | G | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.354-1422C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113494364 | ||||||
| chr9:113494393
|
T | C | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.354-1393T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113494393 | ||||||
| chr9:113494417
|
T | A | 7 | a0001c0011t0001g0071a0002c0004t0002g0073a0002c0004t0002g0094others(4): Show | 7 | HG01243.hp1 HG02572.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.354-1369T>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113494417 | ||||||
| chr9:113494630
|
G | T | 2 | a0001c0001t0001g0047a0003c0020t0001g0048 | 2 | HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.354-1156G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113494630 | ||||||
| chr9:113494862
|
A | ATTC | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | NA18957.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.354-903_354-901dup others(3): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr9 | 113494862 | |||||
| chr9:113494862
|
A | ATTCTTC | 5 | a0001c0001t0003g0038a0001c0001t0003g0044a0001c0001t0003g0045others(2): Show | 5 | HG02055.hp2 HG02717.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.354-906_354-901dup others(6): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr9 | 113494862 | |||||
| chr9:113494862
|
ATTCTTCT others(2): Show |
A | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.354-909_354-901del others(9): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr9 | 113494862 | |||||
| chr9:113494896
|
A | G | 2 | a0001c0001t0001g0158a0001c0002t0007g0164 | 2 | NA18968.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.354-890A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113494896 | ||||||
| chr9:113495372
|
G | T | 6 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(3): Show | 6 | HG01243.hp1 HG02572.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.354-414G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113495372 | ||||||
| chr9:113495461
|
C | T | 1 | a0001c0002t0001g0040 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.354-325C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113495461 | ||||||
| chr9:113495715
|
A | G | 1 | a0001c0001t0001g0132 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.354-71A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 5/22 | chr9 | 113495715 | ||||||
| chr9:113496077
|
C | A | 7 | a0001c0011t0001g0071a0002c0004t0002g0073a0002c0004t0002g0094others(4): Show | 7 | HG01243.hp1 HG02572.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.414+231C>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 6/22 | chr9 | 113496077 | ||||||
| chr9:113496194
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.414+348G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 6/22 | chr9 | 113496194 | ||||||
| chr9:113496275
|
G | A | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.414+429G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 6/22 | chr9 | 113496275 | ||||||
| chr9:113496586
|
T | C | 18 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(15): Show | 18 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.415-728T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 6/22 | chr9 | 113496586 | ||||||
| chr9:113496625
|
G | A | 4 | a0001c0001t0001g0158a0001c0001t0001g0161a0001c0001t0001g0162others(1): Show | 4 | HG00544.hp1 HG00558.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-689G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 6/22 | chr9 | 113496625 | ||||||
| chr9:113496797
|
C | T | 1 | a0001c0001t0003g0068 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.415-517C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 6/22 | chr9 | 113496797 | ||||||
| chr9:113497159
|
G | A | 18 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(15): Show | 18 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.415-155G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 6/22 | chr9 | 113497159 | ||||||
| chr9:113497161
|
T | C | 9 | a0001c0001t0001g0104a0001c0002t0001g0007a0001c0002t0001g0035others(6): Show | 9 | HG00140.hp2 HG00408.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.415-153T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 6/22 | chr9 | 113497161 | ||||||
| chr9:113497470
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.505+66G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 7/22 | chr9 | 113497470 | ||||||
| chr9:113497620
|
T | C | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.505+216T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 7/22 | chr9 | 113497620 | ||||||
| chr9:113497632
|
T | G | 4 | a0002c0005t0002g0013a0002c0005t0002g0014a0002c0005t0003g0010others(1): Show | 4 | HG02970.hp2 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.505+228T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 7/22 | chr9 | 113497632 | ||||||
| chr9:113497659
|
C | G | 51 | a0001c0001t0001g0105a0001c0001t0001g0116a0001c0001t0001g0123others(48): Show | 51 | HG00140.hp1 HG00735.hp1 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.505+255C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 7/22 | chr9 | 113497659 | ||||||
| chr9:113498009
|
C | A | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.506-16C>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 7/22 | chr9 | 113498009 | ||||||
| chr9:113498481
|
A | G | 1 | a0001c0001t0003g0157 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.561+401A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113498481 | ||||||
| chr9:113498485
|
T | G | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.561+405T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113498485 | ||||||
| chr9:113498599
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.561+519G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113498599 | ||||||
| chr9:113498684
|
G | A | 1 | a0001c0011t0001g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.561+604G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113498684 | ||||||
| chr9:113498732
|
C | T | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.561+652C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113498732 | ||||||
| chr9:113498921
|
G | GA | 7 | a0001c0001t0001g0082a0001c0002t0001g0137a0001c0018t0001g0139others(4): Show | 7 | HG00408.hp1 HG01978.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.561+863dupA | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr9 | 113498921 | |||||
| chr9:113498921
|
GA | G | 5 | a0001c0001t0001g0107a0001c0001t0001g0159a0001c0002t0001g0160others(2): Show | 5 | HG01167.hp2 HG01975.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.561+863delA | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr9 | 113498921 | |||||
| chr9:113498948
|
C | T | 2 | a0001c0001t0001g0102a0001c0002t0001g0120 | 2 | HG00408.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.561+868C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113498948 | ||||||
| chr9:113499066
|
A | C | 2 | a0001c0001t0001g0155a0001c0001t0001g0166 | 2 | HG02132.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.561+986A>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113499066 | ||||||
| chr9:113499226
|
C | CA | 21 | a0001c0001t0001g0141a0001c0002t0001g0040a0001c0011t0001g0071others(18): Show | 21 | HG01168.hp2 HG01243.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.561+1167dupA | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr9 | 113499226 | |||||
| chr9:113499226
|
C | CAA | 20 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(17): Show | 20 | HG00140.hp1 HG00741.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.561+1166_561+1167d others(4): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr9 | 113499226 | |||||
| chr9:113499441
|
G | A | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | NA18957.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.561+1361G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113499441 | ||||||
| chr9:113499463
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.561+1383G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113499463 | ||||||
| chr9:113499646
|
T | G | 34 | a0001c0011t0001g0071a0001c0018t0001g0139a0001c0019t0001g0092others(31): Show | 34 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.561+1566T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113499646 | ||||||
| chr9:113499842
|
C | T | 1 | a0001c0011t0001g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.561+1762C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113499842 | ||||||
| chr9:113499941
|
C | T | 1 | a0002c0004t0002g0094 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.561+1861C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113499941 | ||||||
| chr9:113500045
|
G | A | 40 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(37): Show | 40 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.561+1965G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113500045 | ||||||
| chr9:113500687
|
C | CT | 12 | a0001c0001t0001g0049a0001c0001t0001g0091a0001c0001t0002g0060others(9): Show | 12 | HG00741.hp2 HG01106.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.561+2625dupT | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr9 | 113500687 | |||||
| chr9:113500687
|
CT | C | 37 | a0001c0001t0001g0024a0001c0001t0004g0001a0001c0001t0004g0002others(34): Show | 37 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.561+2625delT | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr9 | 113500687 | |||||
| chr9:113500705
|
T | G | 2 | a0001c0018t0001g0139a0001c0019t0001g0092 | 2 | HG02055.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.561+2625T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113500705 | ||||||
| chr9:113500990
|
G | A | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.561+2910G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113500990 | ||||||
| chr9:113501124
|
C | T | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.561+3044C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113501124 | ||||||
| chr9:113501174
|
T | C | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.561+3094T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113501174 | ||||||
| chr9:113501210
|
C | T | 1 | a0001c0007t0001g0115 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.561+3130C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113501210 | ||||||
| chr9:113501303
|
G | T | 1 | a0002c0008t0006g0033 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.561+3223G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113501303 | ||||||
| chr9:113501328
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.561+3248A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113501328 | ||||||
| chr9:113501727
|
T | C | 2 | a0001c0001t0001g0047a0003c0020t0001g0048 | 2 | HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.561+3647T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113501727 | ||||||
| chr9:113501734
|
T | C | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.561+3654T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113501734 | ||||||
| chr9:113501950
|
A | G | 8 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0084others(5): Show | 8 | HG01884.hp1 HG01981.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.562-3492A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113501950 | ||||||
| chr9:113502050
|
G | A | 6 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(3): Show | 6 | HG01243.hp1 HG02572.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.562-3392G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113502050 | ||||||
| chr9:113502336
|
C | T | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.562-3106C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113502336 | ||||||
| chr9:113502467
|
C | T | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.562-2975C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113502467 | ||||||
| chr9:113502595
|
G | A | 38 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(35): Show | 38 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.562-2847G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113502595 | ||||||
| chr9:113502677
|
G | A | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.562-2765G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113502677 | ||||||
| chr9:113502702
|
A | C | 25 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(22): Show | 25 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.562-2740A>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113502702 | ||||||
| chr9:113502702
|
A | T | 7 | a0001c0011t0001g0071a0002c0004t0002g0073a0002c0004t0002g0094others(4): Show | 7 | HG01243.hp1 HG02572.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.562-2740A>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113502702 | ||||||
| chr9:113502808
|
T | C | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.562-2634T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113502808 | ||||||
| chr9:113503080
|
G | A | 41 | a0001c0001t0001g0024a0001c0001t0004g0001a0001c0001t0004g0002others(38): Show | 41 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.562-2362G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113503080 | ||||||
| chr9:113503150
|
C | T | 2 | a0002c0005t0002g0009a0002c0005t0002g0012 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.562-2292C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113503150 | ||||||
| chr9:113503303
|
C | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0086 | 2 | HG01070.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.562-2139C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113503303 | ||||||
| chr9:113503440
|
C | A | 1 | a0001c0001t0001g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.562-2002C>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113503440 | ||||||
| chr9:113503522
|
G | T | 14 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(11): Show | 14 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.562-1920G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113503522 | ||||||
| chr9:113503665
|
G | C | 1 | a0001c0001t0001g0080 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.562-1777G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113503665 | ||||||
| chr9:113503696
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.562-1746G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113503696 | ||||||
| chr9:113503760
|
G | C | 1 | a0001c0001t0001g0085 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.562-1682G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113503760 | ||||||
| chr9:113503821
|
C | G | 2 | a0001c0018t0001g0139a0001c0019t0001g0092 | 2 | HG02055.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.562-1621C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113503821 | ||||||
| chr9:113503843
|
C | T | 6 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(3): Show | 6 | HG01243.hp1 HG02572.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.562-1599C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113503843 | ||||||
| chr9:113503885
|
G | C | 34 | a0001c0011t0001g0071a0001c0018t0001g0139a0001c0019t0001g0092others(31): Show | 34 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.562-1557G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113503885 | ||||||
| chr9:113504142
|
G | C | 7 | a0001c0011t0001g0071a0002c0004t0002g0073a0002c0004t0002g0094others(4): Show | 7 | HG01243.hp1 HG02572.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.562-1300G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113504142 | ||||||
| chr9:113504424
|
A | G | 10 | a0001c0001t0001g0105a0001c0001t0001g0116a0001c0001t0001g0134others(7): Show | 10 | HG00735.hp1 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.562-1018A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113504424 | ||||||
| chr9:113504608
|
C | T | 1 | a0002c0004t0006g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.562-834C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113504608 | ||||||
| chr9:113505036
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.562-406G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113505036 | ||||||
| chr9:113505321
|
C | G | 34 | a0001c0011t0001g0071a0001c0018t0001g0139a0001c0019t0001g0092others(31): Show | 34 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.562-121C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 8/22 | chr9 | 113505321 | ||||||
| chr9:113505549
|
A | G | 34 | a0001c0011t0001g0071a0001c0018t0001g0139a0001c0019t0001g0092others(31): Show | 34 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.643+26A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 9/22 | chr9 | 113505549 | ||||||
| chr9:113505837
|
A | G | 14 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(11): Show | 14 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.643+314A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 9/22 | chr9 | 113505837 | ||||||
| chr9:113505851
|
T | C | 34 | a0001c0011t0001g0071a0001c0018t0001g0139a0001c0019t0001g0092others(31): Show | 34 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.643+328T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 9/22 | chr9 | 113505851 | ||||||
| chr9:113506010
|
G | A | 2 | a0002c0005t0002g0009a0002c0005t0002g0012 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.644-378G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 9/22 | chr9 | 113506010 | ||||||
| chr9:113506144
|
A | G | 18 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(15): Show | 18 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.644-244A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 9/22 | chr9 | 113506144 | ||||||
| chr9:113506199
|
A | G | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.644-189A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 9/22 | chr9 | 113506199 | ||||||
| chr9:113506301
|
G | A | 1 | a0004c0009t0001g0121 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.644-87G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 9/22 | chr9 | 113506301 | ||||||
| chr9:113506326
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.644-62A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 9/22 | chr9 | 113506326 | ||||||
| chr9:113506576
|
C | T | 1 | a0001c0013t0001g0142 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.749+83C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 10/22 | chr9 | 113506576 | ||||||
| chr9:113506814
|
G | A | 34 | a0001c0011t0001g0071a0001c0018t0001g0139a0001c0019t0001g0092others(31): Show | 34 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.749+321G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 10/22 | chr9 | 113506814 | ||||||
| chr9:113506816
|
A | T | 1 | a0001c0011t0001g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.749+323A>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 10/22 | chr9 | 113506816 | ||||||
| chr9:113507023
|
T | G | 2 | a0001c0018t0001g0139a0001c0019t0001g0092 | 2 | HG02055.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.750-264T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 10/22 | chr9 | 113507023 | ||||||
| chr9:113507174
|
T | C | 40 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(37): Show | 40 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.750-113T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 10/22 | chr9 | 113507174 | ||||||
| chr9:113507186
|
C | G | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.750-101C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 10/22 | chr9 | 113507186 | ||||||
| chr9:113507240
|
T | G | 34 | a0001c0011t0001g0071a0001c0018t0001g0139a0001c0019t0001g0092others(31): Show | 34 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.750-47T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 10/22 | chr9 | 113507240 | ||||||
| chr9:113507909
|
C | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG00544.hp1 HG00558.hp1 |
intron_variant | MODIFIER | c.1101+271C>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 11/22 | chr9 | 113507909 | ||||||
| chr9:113507936
|
G | T | 2 | a0001c0018t0001g0139a0001c0019t0001g0092 | 2 | HG02055.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1101+298G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 11/22 | chr9 | 113507936 | ||||||
| chr9:113508016
|
G | A | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1101+378G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 11/22 | chr9 | 113508016 | ||||||
| chr9:113508133
|
G | A | 2 | a0001c0018t0001g0139a0001c0019t0001g0092 | 2 | HG02055.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1102-408G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 11/22 | chr9 | 113508133 | ||||||
| chr9:113508374
|
G | A | 6 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(3): Show | 6 | HG01243.hp1 HG02572.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1102-167G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 11/22 | chr9 | 113508374 | ||||||
| chr9:113508656
|
C | T | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1141+76C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113508656 | ||||||
| chr9:113508696
|
C | A | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1141+116C>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113508696 | ||||||
| chr9:113508727
|
G | C | 1 | a0001c0002t0001g0138 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1141+147G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113508727 | ||||||
| chr9:113509113
|
G | A | 3 | a0002c0004t0002g0094a0002c0004t0002g0095a0002c0004t0002g0096 | 3 | HG01243.hp1 HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1141+533G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113509113 | ||||||
| chr9:113509145
|
C | T | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1141+565C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113509145 | ||||||
| chr9:113509158
|
G | A | 1 | a0001c0013t0001g0142 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1141+578G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113509158 | ||||||
| chr9:113509283
|
T | TA | 5 | a0001c0001t0001g0008a0001c0001t0001g0082a0001c0001t0001g0128others(2): Show | 5 | HG00408.hp1 HG01978.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1141+718dupA | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr9 | 113509283 | |||||
| chr9:113509283
|
TA | T | 6 | a0001c0001t0001g0043a0001c0001t0001g0107a0001c0001t0003g0038others(3): Show | 6 | HG01975.hp2 HG02055.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1141+718delA | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr9 | 113509283 | |||||
| chr9:113509699
|
A | T | 4 | a0002c0005t0002g0013a0002c0005t0002g0014a0002c0005t0003g0010others(1): Show | 4 | HG02970.hp2 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1141+1119A>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113509699 | ||||||
| chr9:113509738
|
C | T | 19 | a0001c0001t0001g0008a0001c0001t0001g0072a0001c0001t0001g0082others(16): Show | 19 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.1141+1158C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113509738 | ||||||
| chr9:113509750
|
G | C | 34 | a0001c0011t0001g0071a0001c0018t0001g0139a0001c0019t0001g0092others(31): Show | 34 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1141+1170G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113509750 | ||||||
| chr9:113509917
|
G | A | 1 | a0001c0001t0003g0044 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1141+1337G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113509917 | ||||||
| chr9:113510050
|
T | C | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1141+1470T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113510050 | ||||||
| chr9:113510087
|
C | T | 2 | a0001c0001t0001g0110a0001c0001t0001g0141 | 2 | HG01981.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1141+1507C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113510087 | ||||||
| chr9:113510122
|
G | C | 34 | a0001c0011t0001g0071a0001c0018t0001g0139a0001c0019t0001g0092others(31): Show | 34 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1141+1542G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113510122 | ||||||
| chr9:113510401
|
T | C | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1141+1821T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113510401 | ||||||
| chr9:113510621
|
C | A | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1141+2041C>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113510621 | ||||||
| chr9:113510971
|
C | T | 1 | a0001c0011t0001g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1141+2391C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113510971 | ||||||
| chr9:113511142
|
C | T | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1141+2562C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113511142 | ||||||
| chr9:113511401
|
T | TA | 13 | a0001c0011t0001g0071a0002c0003t0002g0077a0002c0003t0002g0078others(10): Show | 13 | HG01243.hp1 HG01884.hp2 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.1141+2836dupA | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr9 | 113511401 | |||||
| chr9:113511401
|
TA | T | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1141+2836delA | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr9 | 113511401 | |||||
| chr9:113511920
|
G | C | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1142-2538G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113511920 | ||||||
| chr9:113512078
|
G | A | 19 | a0001c0001t0001g0008a0001c0001t0001g0072a0001c0001t0001g0082others(16): Show | 19 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.1142-2380G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113512078 | ||||||
| chr9:113512199
|
G | A | 4 | a0002c0004t0006g0018a0002c0004t0006g0023a0002c0008t0006g0033others(1): Show | 4 | HG01978.hp2 HG02922.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1142-2259G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113512199 | ||||||
| chr9:113512264
|
C | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0084 | 3 | HG02559.hp1 HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1142-2194C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113512264 | ||||||
| chr9:113512300
|
A | G | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1142-2158A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113512300 | ||||||
| chr9:113512493
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1142-1965C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113512493 | ||||||
| chr9:113512558
|
G | A | 6 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(3): Show | 6 | HG01243.hp1 HG02572.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1142-1900G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113512558 | ||||||
| chr9:113512572
|
T | G | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | NA18957.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1142-1886T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113512572 | ||||||
| chr9:113512652
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1142-1806C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113512652 | ||||||
| chr9:113512654
|
T | G | 40 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(37): Show | 40 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.1142-1804T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113512654 | ||||||
| chr9:113512661
|
C | T | 1 | a0001c0011t0001g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1142-1797C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113512661 | ||||||
| chr9:113512666
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1142-1792G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113512666 | ||||||
| chr9:113512712
|
A | T | 1 | a0001c0001t0001g0158 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1142-1746A>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113512712 | ||||||
| chr9:113512858
|
G | A | 2 | a0002c0008t0006g0033a0002c0008t0006g0034 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1142-1600G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113512858 | ||||||
| chr9:113512889
|
C | T | 1 | a0002c0005t0002g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1142-1569C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113512889 | ||||||
| chr9:113512995
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1142-1463G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113512995 | ||||||
| chr9:113513013
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1142-1445A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113513013 | ||||||
| chr9:113513053
|
G | A | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1142-1405G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113513053 | ||||||
| chr9:113513228
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1142-1230G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113513228 | ||||||
| chr9:113513240
|
C | G | 14 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(11): Show | 14 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.1142-1218C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113513240 | ||||||
| chr9:113513295
|
T | TC | 25 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(22): Show | 25 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1142-1157dupC | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr9 | 113513295 | |||||
| chr9:113513300
|
C | CT | 7 | a0001c0011t0001g0071a0002c0004t0002g0073a0002c0004t0002g0094others(4): Show | 7 | HG01243.hp1 HG02572.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1142-1158_1142-115 others(5): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113513300 | ||||||
| chr9:113513302
|
A | C | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1142-1156A>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113513302 | ||||||
| chr9:113513588
|
T | TA | 2 | a0001c0001t0001g0110a0001c0001t0001g0141 | 2 | HG01981.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1142-869dupA | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr9 | 113513588 | |||||
| chr9:113513775
|
A | G | 3 | a0002c0004t0002g0094a0002c0004t0002g0095a0002c0004t0002g0096 | 3 | HG01243.hp1 HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1142-683A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113513775 | ||||||
| chr9:113514000
|
C | T | 1 | a0001c0001t0003g0046 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1142-458C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113514000 | ||||||
| chr9:113514298
|
A | G | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1142-160A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113514298 | ||||||
| chr9:113514301
|
C | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0111a0001c0001t0001g0117 | 3 | HG01928.hp2 HG02698.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1142-157C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 12/22 | chr9 | 113514301 | ||||||
| chr9:113514662
|
C | G | 3 | a0001c0001t0001g0043a0001c0001t0001g0049a0001c0001t0001g0159 | 3 | HG02717.hp1 HG02922.hp1 HG02976.hp2 |
splice_region_variant&intron_variant | LOW | c.1338+8C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 13/22 | chr9 | 113514662 | ||||||
| chr9:113514704
|
A | T | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1338+50A>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 13/22 | chr9 | 113514704 | ||||||
| chr9:113514752
|
T | C | 18 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(15): Show | 18 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1338+98T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 13/22 | chr9 | 113514752 | ||||||
| chr9:113514828
|
T | A | 3 | a0001c0001t0001g0144a0001c0002t0001g0146a0001c0002t0001g0147 | 3 | HG01109.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1338+174T>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 13/22 | chr9 | 113514828 | ||||||
| chr9:113515108
|
C | T | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1338+454C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 13/22 | chr9 | 113515108 | ||||||
| chr9:113515245
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1338+591C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 13/22 | chr9 | 113515245 | ||||||
| chr9:113515482
|
T | G | 1 | a0001c0019t0001g0092 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1338+828T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 13/22 | chr9 | 113515482 | ||||||
| chr9:113515683
|
C | A | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1338+1029C>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 13/22 | chr9 | 113515683 | ||||||
| chr9:113515747
|
C | T | 1 | a0001c0011t0001g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1338+1093C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 13/22 | chr9 | 113515747 | ||||||
| chr9:113515824
|
C | T | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1338+1170C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 13/22 | chr9 | 113515824 | ||||||
| chr9:113515838
|
G | T | 2 | a0001c0001t0001g0140a0001c0015t0001g0136 | 2 | HG00639.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1338+1184G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 13/22 | chr9 | 113515838 | ||||||
| chr9:113515955
|
G | A | 6 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(3): Show | 6 | HG01243.hp1 HG02572.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1338+1301G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 13/22 | chr9 | 113515955 | ||||||
| chr9:113515960
|
G | A | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1338+1306G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 13/22 | chr9 | 113515960 | ||||||
| chr9:113516420
|
C | T | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1339-1121C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 13/22 | chr9 | 113516420 | ||||||
| chr9:113516693
|
A | G | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1339-848A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 13/22 | chr9 | 113516693 | ||||||
| chr9:113516787
|
C | T | 2 | a0001c0001t0001g0127a0001c0001t0001g0133 | 2 | NA18747.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1339-754C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 13/22 | chr9 | 113516787 | ||||||
| chr9:113516988
|
C | G | 6 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(3): Show | 6 | HG01243.hp1 HG02572.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1339-553C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 13/22 | chr9 | 113516988 | ||||||
| chr9:113517045
|
T | C | 2 | a0001c0018t0001g0139a0001c0019t0001g0092 | 2 | HG02055.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1339-496T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 13/22 | chr9 | 113517045 | ||||||
| chr9:113517132
|
A | G | 6 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(3): Show | 6 | HG01243.hp1 HG02572.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1339-409A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 13/22 | chr9 | 113517132 | ||||||
| chr9:113517227
|
G | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | NA18957.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1339-314G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 13/22 | chr9 | 113517227 | ||||||
| chr9:113517415
|
C | T | 1 | a0001c0002t0001g0120 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1339-126C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 13/22 | chr9 | 113517415 | ||||||
| chr9:113517421
|
G | T | 25 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(22): Show | 25 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1339-120G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 13/22 | chr9 | 113517421 | ||||||
| chr9:113517823
|
C | T | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1422+199C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113517823 | ||||||
| chr9:113517924
|
T | C | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1422+300T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113517924 | ||||||
| chr9:113517934
|
G | A | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1422+310G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113517934 | ||||||
| chr9:113517939
|
A | G | 1 | a0002c0004t0002g0098 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1422+315A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113517939 | ||||||
| chr9:113518034
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1422+410C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113518034 | ||||||
| chr9:113518088
|
C | A | 1 | a0001c0011t0001g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1422+464C>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113518088 | ||||||
| chr9:113518262
|
C | G | 3 | a0002c0004t0002g0073a0002c0004t0002g0097a0002c0004t0002g0098 | 3 | HG06807.hp2 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1422+638C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113518262 | ||||||
| chr9:113518492
|
A | G | 1 | a0001c0018t0001g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1422+868A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113518492 | ||||||
| chr9:113518671
|
C | T | 4 | a0002c0004t0006g0018a0002c0004t0006g0023a0002c0008t0006g0033others(1): Show | 4 | HG01978.hp2 HG02922.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1422+1047C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113518671 | ||||||
| chr9:113518679
|
G | A | 1 | a0002c0003t0002g0032 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1422+1055G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113518679 | ||||||
| chr9:113518696
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1422+1072G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113518696 | ||||||
| chr9:113518719
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1422+1095C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113518719 | ||||||
| chr9:113519510
|
C | CA | 6 | a0001c0001t0001g0064a0001c0001t0001g0090a0001c0001t0001g0132others(3): Show | 6 | HG00621.hp1 HG01243.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.1422+1907dupA | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr9 | 113519510 | |||||
| chr9:113519510
|
CA | C | 19 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0001g0085others(16): Show | 19 | HG00738.hp1 HG01167.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.1422+1907delA | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr9 | 113519510 | |||||
| chr9:113519510
|
CAAAAAAA | C | 11 | a0001c0001t0003g0026a0001c0001t0003g0038a0001c0001t0003g0044others(8): Show | 11 | HG01081.hp1 HG01081.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1422+1901_1422+190 others(11): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr9 | 113519510 | |||||
| chr9:113519677
|
T | G | 2 | a0001c0001t0001g0042a0001c0001t0001g0163 | 2 | NA18997.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.1422+2053T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113519677 | ||||||
| chr9:113519679
|
G | GT | 8 | a0001c0001t0001g0008a0001c0001t0001g0088a0001c0001t0004g0001others(5): Show | 8 | HG00544.hp2 HG02132.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.1422+2066dupT | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr9 | 113519679 | |||||
| chr9:113519679
|
GT | G | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1422+2066delT | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr9 | 113519679 | |||||
| chr9:113519697
|
A | G | 40 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(37): Show | 40 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.1422+2073A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113519697 | ||||||
| chr9:113519704
|
A | G | 1 | a0001c0018t0001g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1422+2080A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113519704 | ||||||
| chr9:113519834
|
G | A | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1422+2210G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113519834 | ||||||
| chr9:113519834
|
G | T | 1 | a0001c0013t0001g0142 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1422+2210G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113519834 | ||||||
| chr9:113520026
|
C | T | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1422+2402C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113520026 | ||||||
| chr9:113520306
|
G | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0143 | 2 | HG02040.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1423-2624G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113520306 | ||||||
| chr9:113520481
|
T | C | 1 | a0002c0003t0002g0029 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1423-2449T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113520481 | ||||||
| chr9:113520542
|
G | GT | 8 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0108others(5): Show | 8 | HG01243.hp1 HG01928.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.1423-2366dupT | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr9 | 113520542 | |||||
| chr9:113520542
|
GT | G | 5 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0004others(2): Show | 5 | HG01168.hp2 HG02132.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.1423-2366delT | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr9 | 113520542 | |||||
| chr9:113520551
|
T | G | 11 | a0001c0001t0001g0105a0001c0001t0001g0116a0001c0001t0001g0123others(8): Show | 11 | HG00735.hp1 HG00738.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.1423-2379T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113520551 | ||||||
| chr9:113520593
|
G | A | 2 | a0001c0001t0002g0036a0001c0001t0002g0037 | 2 | HG01516.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1423-2337G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113520593 | ||||||
| chr9:113520671
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1423-2259T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113520671 | ||||||
| chr9:113520927
|
T | C | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1423-2003T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113520927 | ||||||
| chr9:113521087
|
G | T | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1423-1843G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113521087 | ||||||
| chr9:113521103
|
G | A | 3 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0125 | 3 | HG02109.hp2 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1423-1827G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113521103 | ||||||
| chr9:113521235
|
A | T | 2 | a0001c0002t0001g0007a0001c0002t0001g0126 | 2 | HG02040.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1423-1695A>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113521235 | ||||||
| chr9:113521450
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1423-1480A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113521450 | ||||||
| chr9:113521751
|
T | C | 7 | a0001c0011t0001g0071a0002c0004t0002g0073a0002c0004t0002g0094others(4): Show | 7 | HG01243.hp1 HG02572.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1423-1179T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113521751 | ||||||
| chr9:113522457
|
C | A | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1423-473C>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113522457 | ||||||
| chr9:113522613
|
C | G | 32 | a0001c0011t0001g0071a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1423-317C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113522613 | ||||||
| chr9:113522803
|
T | C | 33 | a0001c0001t0001g0017a0001c0011t0001g0071a0002c0003t0002g0029others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1423-127T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113522803 | ||||||
| chr9:113522849
|
C | T | 1 | a0001c0001t0004g0001 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1423-81C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 14/22 | chr9 | 113522849 | ||||||
| chr9:113523149
|
T | C | 33 | a0001c0001t0001g0017a0001c0011t0001g0071a0002c0003t0002g0029others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1534+108T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113523149 | ||||||
| chr9:113523283
|
A | G | 4 | a0001c0001t0001g0158a0001c0001t0001g0161a0001c0001t0001g0162others(1): Show | 4 | HG00544.hp1 HG00558.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.1534+242A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113523283 | ||||||
| chr9:113523680
|
G | A | 1 | a0001c0001t0001g0085 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1534+639G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113523680 | ||||||
| chr9:113523922
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1534+881A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113523922 | ||||||
| chr9:113523934
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1534+893G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113523934 | ||||||
| chr9:113524170
|
G | A | 1 | a0002c0008t0006g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1534+1129G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113524170 | ||||||
| chr9:113524189
|
T | C | 34 | a0001c0001t0001g0017a0001c0001t0001g0047a0001c0011t0001g0071others(31): Show | 34 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1534+1148T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113524189 | ||||||
| chr9:113524210
|
C | G | 19 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(16): Show | 19 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.1534+1169C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113524210 | ||||||
| chr9:113524460
|
A | G | 33 | a0001c0001t0001g0017a0001c0011t0001g0071a0002c0003t0002g0029others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1534+1419A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113524460 | ||||||
| chr9:113524820
|
T | A | 33 | a0001c0001t0001g0017a0001c0011t0001g0071a0002c0003t0002g0029others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1534+1779T>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113524820 | ||||||
| chr9:113524866
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1534+1825G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113524866 | ||||||
| chr9:113524993
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1534+1952G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113524993 | ||||||
| chr9:113525071
|
T | C | 39 | a0001c0001t0001g0017a0001c0001t0004g0001a0001c0001t0004g0002others(36): Show | 39 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1534+2030T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113525071 | ||||||
| chr9:113525287
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1534+2246C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113525287 | ||||||
| chr9:113525337
|
T | C | 2 | a0001c0018t0001g0139a0001c0019t0001g0092 | 2 | HG02055.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1534+2296T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113525337 | ||||||
| chr9:113525398
|
C | T | 3 | a0001c0001t0001g0144a0001c0002t0001g0146a0001c0002t0001g0147 | 3 | HG01109.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1534+2357C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113525398 | ||||||
| chr9:113525883
|
G | A | 1 | a0001c0011t0001g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1534+2842G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113525883 | ||||||
| chr9:113525957
|
C | T | 1 | a0001c0002t0001g0120 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1534+2916C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113525957 | ||||||
| chr9:113525984
|
T | C | 41 | a0001c0001t0001g0017a0001c0001t0004g0001a0001c0001t0004g0002others(38): Show | 41 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1534+2943T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113525984 | ||||||
| chr9:113526085
|
C | T | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1534+3044C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113526085 | ||||||
| chr9:113526140
|
A | T | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1535-3081A>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113526140 | ||||||
| chr9:113526193
|
T | C | 33 | a0001c0001t0001g0017a0001c0011t0001g0071a0002c0003t0002g0029others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1535-3028T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113526193 | ||||||
| chr9:113526257
|
T | C | 41 | a0001c0001t0001g0017a0001c0001t0004g0001a0001c0001t0004g0002others(38): Show | 41 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1535-2964T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113526257 | ||||||
| chr9:113526318
|
T | C | 158 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0024others(155): Show | 158 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.1535-2903T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113526318 | ||||||
| chr9:113526319
|
G | A | 1 | a0001c0001t0003g0045 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1535-2902G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113526319 | ||||||
| chr9:113526376
|
C | T | 2 | a0001c0018t0001g0139a0001c0019t0001g0092 | 2 | HG02055.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1535-2845C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113526376 | ||||||
| chr9:113526450
|
T | C | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1535-2771T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113526450 | ||||||
| chr9:113526495
|
C | T | 33 | a0001c0001t0001g0017a0001c0011t0001g0071a0002c0003t0002g0029others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1535-2726C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113526495 | ||||||
| chr9:113526663
|
G | A | 33 | a0001c0001t0001g0017a0001c0011t0001g0071a0002c0003t0002g0029others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1535-2558G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113526663 | ||||||
| chr9:113526710
|
T | C | 1 | a0001c0002t0001g0137 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1535-2511T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113526710 | ||||||
| chr9:113526717
|
C | T | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1535-2504C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113526717 | ||||||
| chr9:113526769
|
C | A | 3 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0125 | 3 | HG02109.hp2 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1535-2452C>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113526769 | ||||||
| chr9:113526769
|
C | T | 2 | a0001c0018t0001g0139a0001c0019t0001g0092 | 2 | HG02055.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1535-2452C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113526769 | ||||||
| chr9:113527084
|
G | A | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1535-2137G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113527084 | ||||||
| chr9:113527137
|
G | A | 33 | a0001c0001t0001g0017a0001c0011t0001g0071a0002c0003t0002g0029others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1535-2084G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113527137 | ||||||
| chr9:113527223
|
C | T | 2 | a0002c0004t0006g0018a0002c0004t0006g0023 | 2 | HG01978.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1535-1998C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113527223 | ||||||
| chr9:113527636
|
C | G | 33 | a0001c0001t0001g0017a0001c0011t0001g0071a0002c0003t0002g0029others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1535-1585C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113527636 | ||||||
| chr9:113527904
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1535-1317G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113527904 | ||||||
| chr9:113528157
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1535-1064G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113528157 | ||||||
| chr9:113528483
|
C | G | 19 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(16): Show | 19 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.1535-738C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113528483 | ||||||
| chr9:113528491
|
C | G | 6 | a0001c0001t0001g0072a0001c0001t0001g0099a0001c0001t0001g0100others(3): Show | 6 | HG00408.hp2 HG00621.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.1535-730C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113528491 | ||||||
| chr9:113528546
|
C | T | 14 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(11): Show | 14 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.1535-675C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113528546 | ||||||
| chr9:113528553
|
G | A | 2 | a0001c0018t0001g0139a0001c0019t0001g0092 | 2 | HG02055.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1535-668G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113528553 | ||||||
| chr9:113528650
|
C | G | 1 | a0001c0001t0001g0017 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1535-571C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113528650 | ||||||
| chr9:113529052
|
C | T | 5 | a0002c0005t0002g0013a0002c0005t0002g0014a0002c0005t0003g0010others(2): Show | 5 | HG02818.hp2 HG02970.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1535-169C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113529052 | ||||||
| chr9:113529110
|
C | T | 33 | a0001c0001t0001g0017a0001c0011t0001g0071a0002c0003t0002g0029others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1535-111C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 15/22 | chr9 | 113529110 | ||||||
| chr9:113529876
|
C | T | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1578+612C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113529876 | ||||||
| chr9:113529927
|
T | C | 19 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(16): Show | 19 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.1578+663T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113529927 | ||||||
| chr9:113530057
|
C | T | 2 | a0002c0005t0002g0009a0002c0005t0002g0012 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1578+793C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113530057 | ||||||
| chr9:113530204
|
A | G | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1578+940A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113530204 | ||||||
| chr9:113530737
|
C | G | 33 | a0001c0001t0001g0017a0001c0011t0001g0071a0002c0003t0002g0029others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1578+1473C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113530737 | ||||||
| chr9:113530819
|
C | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0141 | 2 | HG01981.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1578+1555C>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113530819 | ||||||
| chr9:113530824
|
C | G | 6 | a0001c0001t0001g0082a0001c0001t0001g0128a0001c0001t0001g0130others(3): Show | 6 | HG00558.hp2 HG01928.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1578+1560C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113530824 | ||||||
| chr9:113531070
|
C | G | 1 | a0001c0001t0001g0111 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1578+1806C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113531070 | ||||||
| chr9:113531227
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1578+1963C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113531227 | ||||||
| chr9:113531516
|
G | A | 1 | a0001c0001t0001g0085 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1578+2252G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113531516 | ||||||
| chr9:113531576
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1578+2312A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113531576 | ||||||
| chr9:113531667
|
G | A | 7 | a0001c0006t0001g0028a0001c0006t0001g0041a0001c0006t0001g0052others(4): Show | 7 | HG02109.hp1 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1578+2403G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113531667 | ||||||
| chr9:113531732
|
A | C | 1 | a0001c0001t0001g0122 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1578+2468A>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113531732 | ||||||
| chr9:113532126
|
C | T | 2 | a0001c0001t0001g0107a0001c0002t0001g0106 | 2 | HG01258.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1578+2862C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113532126 | ||||||
| chr9:113532237
|
C | T | 33 | a0001c0001t0001g0017a0001c0011t0001g0071a0002c0003t0002g0029others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1578+2973C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113532237 | ||||||
| chr9:113532378
|
AAG | A | 33 | a0001c0001t0001g0017a0001c0011t0001g0071a0002c0003t0002g0029others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1578+3126_1578+312 others(6): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr9 | 113532378 | |||||
| chr9:113532404
|
T | G | 1 | a0001c0018t0001g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1578+3140T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113532404 | ||||||
| chr9:113532409
|
C | T | 1 | a0001c0002t0001g0040 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1578+3145C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113532409 | ||||||
| chr9:113532621
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0143 | 2 | HG02040.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1578+3357G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113532621 | ||||||
| chr9:113532647
|
A | G | 1 | a0001c0002t0001g0079 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1578+3383A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113532647 | ||||||
| chr9:113532736
|
G | T | 7 | a0001c0011t0001g0071a0002c0004t0002g0073a0002c0004t0002g0094others(4): Show | 7 | HG01243.hp1 HG02572.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1578+3472G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113532736 | ||||||
| chr9:113532787
|
C | G | 1 | a0001c0002t0001g0147 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1578+3523C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113532787 | ||||||
| chr9:113532893
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1578+3629C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113532893 | ||||||
| chr9:113532992
|
G | A | 1 | a0002c0008t0006g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1578+3728G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113532992 | ||||||
| chr9:113533216
|
G | A | 33 | a0001c0001t0001g0017a0001c0011t0001g0071a0002c0003t0002g0029others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1579-3580G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113533216 | ||||||
| chr9:113533233
|
G | GT | 26 | a0001c0001t0001g0017a0001c0001t0004g0001a0001c0001t0004g0002others(23): Show | 26 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1579-3548dupT | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr9 | 113533233 | |||||
| chr9:113533233
|
G | GTT | 15 | a0001c0018t0001g0139a0001c0019t0001g0092a0002c0004t0002g0073others(12): Show | 15 | HG01243.hp1 HG02055.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1579-3549_1579-354 others(6): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr9 | 113533233 | |||||
| chr9:113533334
|
G | T | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1579-3462G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113533334 | ||||||
| chr9:113533419
|
C | T | 2 | a0001c0001t0001g0110a0001c0001t0001g0141 | 2 | HG01981.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1579-3377C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113533419 | ||||||
| chr9:113533521
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1579-3275G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113533521 | ||||||
| chr9:113533688
|
C | T | 3 | a0001c0001t0001g0017a0002c0004t0006g0018a0002c0004t0006g0023 | 3 | HG01978.hp2 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1579-3108C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113533688 | ||||||
| chr9:113533830
|
C | T | 1 | a0002c0005t0008g0015 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1579-2966C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113533830 | ||||||
| chr9:113534112
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1579-2684T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113534112 | ||||||
| chr9:113534443
|
G | A | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1579-2353G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113534443 | ||||||
| chr9:113534533
|
G | A | 29 | a0001c0001t0001g0017a0001c0011t0001g0071a0002c0003t0002g0029others(26): Show | 29 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.1579-2263G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113534533 | ||||||
| chr9:113534610
|
A | AT | 5 | a0001c0001t0001g0024a0001c0001t0003g0070a0001c0001t0003g0157others(2): Show | 5 | HG01081.hp1 HG01081.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1579-2166dupT | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr9 | 113534610 | |||||
| chr9:113534610
|
AT | A | 69 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0039others(66): Show | 69 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.1579-2166delT | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr9 | 113534610 | |||||
| chr9:113534610
|
ATT | A | 31 | a0001c0001t0001g0017a0001c0011t0001g0071a0002c0003t0002g0029others(28): Show | 31 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.1579-2167_1579-216 others(6): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr9 | 113534610 | |||||
| chr9:113534757
|
G | A | 1 | a0001c0011t0001g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1579-2039G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113534757 | ||||||
| chr9:113534875
|
C | T | 33 | a0001c0001t0001g0017a0001c0011t0001g0071a0002c0003t0002g0029others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1579-1921C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113534875 | ||||||
| chr9:113535184
|
T | C | 33 | a0001c0001t0001g0017a0001c0011t0001g0071a0002c0003t0002g0029others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1579-1612T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113535184 | ||||||
| chr9:113535238
|
A | G | 6 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(3): Show | 6 | HG01243.hp1 HG02572.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1579-1558A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113535238 | ||||||
| chr9:113535392
|
C | T | 6 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(3): Show | 6 | HG01243.hp1 HG02572.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1579-1404C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113535392 | ||||||
| chr9:113535417
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0086 | 2 | HG01070.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1579-1379C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113535417 | ||||||
| chr9:113535582
|
T | C | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | NA18962.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1579-1214T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113535582 | ||||||
| chr9:113535697
|
G | A | 2 | a0002c0004t0006g0018a0002c0004t0006g0023 | 2 | HG01978.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1579-1099G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113535697 | ||||||
| chr9:113535715
|
CT | C | 34 | a0001c0001t0001g0017a0001c0001t0004g0004a0001c0011t0001g0071others(31): Show | 34 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1579-1071delT | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr9 | 113535715 | |||||
| chr9:113535801
|
C | A | 2 | a0002c0005t0002g0009a0002c0005t0002g0012 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1579-995C>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113535801 | ||||||
| chr9:113535851
|
C | T | 1 | a0001c0011t0001g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1579-945C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113535851 | ||||||
| chr9:113536313
|
G | A | 5 | a0001c0001t0001g0107a0001c0001t0004g0001a0001c0001t0004g0002others(2): Show | 5 | HG00408.hp1 HG01258.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1579-483G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113536313 | ||||||
| chr9:113536385
|
A | G | 30 | a0001c0001t0001g0017a0001c0001t0001g0108a0001c0018t0001g0139others(27): Show | 30 | HG00140.hp1 HG00738.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.1579-411A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113536385 | ||||||
| chr9:113536515
|
CCTG | C | 2 | a0002c0008t0006g0033a0002c0008t0006g0034 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1579-278_1579-276d others(5): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr9 | 113536515 | |||||
| chr9:113536620
|
C | T | 28 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(25): Show | 28 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.1579-176C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113536620 | ||||||
| chr9:113536637
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1579-159A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 16/22 | chr9 | 113536637 | ||||||
| chr9:113536956
|
G | A | 2 | a0002c0003t0002g0077a0002c0003t0002g0078 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1701+38G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113536956 | ||||||
| chr9:113537207
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1701+289C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113537207 | ||||||
| chr9:113537617
|
A | G | 1 | a0001c0002t0001g0093 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1701+699A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113537617 | ||||||
| chr9:113537673
|
G | T | 14 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(11): Show | 14 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.1701+755G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113537673 | ||||||
| chr9:113537899
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1701+981C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113537899 | ||||||
| chr9:113538373
|
G | A | 6 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(3): Show | 6 | HG01243.hp1 HG02572.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1701+1455G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113538373 | ||||||
| chr9:113538487
|
G | A | 33 | a0001c0001t0001g0017a0001c0011t0001g0071a0002c0003t0002g0029others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1701+1569G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113538487 | ||||||
| chr9:113538518
|
T | C | 1 | a0001c0011t0001g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1701+1600T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113538518 | ||||||
| chr9:113538656
|
C | G | 39 | a0001c0001t0001g0017a0001c0001t0004g0001a0001c0001t0004g0002others(36): Show | 39 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1701+1738C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113538656 | ||||||
| chr9:113538843
|
C | T | 9 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0125others(6): Show | 9 | HG01243.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1701+1925C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113538843 | ||||||
| chr9:113538883
|
C | G | 12 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0154others(9): Show | 12 | HG00544.hp1 HG00558.hp1 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.1701+1965C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113538883 | ||||||
| chr9:113538989
|
A | G | 7 | a0001c0011t0001g0071a0002c0004t0002g0073a0002c0004t0002g0094others(4): Show | 7 | HG01243.hp1 HG02572.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1701+2071A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113538989 | ||||||
| chr9:113539029
|
T | G | 1 | a0001c0001t0001g0130 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1701+2111T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113539029 | ||||||
| chr9:113539169
|
C | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0111a0001c0001t0001g0117 | 3 | HG01928.hp2 HG02698.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1701+2251C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113539169 | ||||||
| chr9:113539189
|
G | A | 3 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0125 | 3 | HG02109.hp2 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1701+2271G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113539189 | ||||||
| chr9:113539266
|
G | A | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1701+2348G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113539266 | ||||||
| chr9:113539676
|
G | T | 1 | a0001c0001t0001g0050 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1701+2758G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113539676 | ||||||
| chr9:113540102
|
G | C | 38 | a0001c0001t0001g0017a0001c0001t0004g0001a0001c0001t0004g0002others(35): Show | 38 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.1701+3184G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113540102 | ||||||
| chr9:113540514
|
C | T | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1701+3596C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113540514 | ||||||
| chr9:113540535
|
C | T | 32 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1701+3617C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113540535 | ||||||
| chr9:113540696
|
G | T | 32 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1701+3778G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113540696 | ||||||
| chr9:113540757
|
A | G | 41 | a0001c0001t0001g0017a0001c0001t0004g0001a0001c0001t0004g0002others(38): Show | 41 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1701+3839A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113540757 | ||||||
| chr9:113540775
|
T | A | 1 | a0001c0001t0001g0086 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1701+3857T>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113540775 | ||||||
| chr9:113540784
|
G | A | 32 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1701+3866G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113540784 | ||||||
| chr9:113541607
|
T | C | 2 | a0002c0003t0002g0077a0002c0003t0002g0078 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1701+4689T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113541607 | ||||||
| chr9:113541667
|
C | G | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1701+4749C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113541667 | ||||||
| chr9:113541835
|
C | G | 1 | a0001c0001t0001g0149 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1701+4917C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113541835 | ||||||
| chr9:113541885
|
G | A | 32 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1701+4967G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113541885 | ||||||
| chr9:113542024
|
G | A | 42 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0004g0001others(39): Show | 42 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.1701+5106G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113542024 | ||||||
| chr9:113542048
|
T | A | 1 | a0001c0001t0001g0123 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1701+5130T>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113542048 | ||||||
| chr9:113542049
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1701+5131G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113542049 | ||||||
| chr9:113542369
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1701+5451C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113542369 | ||||||
| chr9:113542633
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1701+5715T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113542633 | ||||||
| chr9:113542672
|
G | A | 32 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1701+5754G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113542672 | ||||||
| chr9:113542786
|
G | A | 2 | a0001c0018t0001g0139a0001c0019t0001g0092 | 2 | HG02055.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1701+5868G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113542786 | ||||||
| chr9:113542863
|
C | G | 2 | a0001c0018t0001g0139a0001c0019t0001g0092 | 2 | HG02055.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1701+5945C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113542863 | ||||||
| chr9:113542919
|
A | C | 1 | a0001c0001t0001g0150 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1701+6001A>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113542919 | ||||||
| chr9:113543532
|
G | A | 32 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1701+6614G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113543532 | ||||||
| chr9:113543709
|
A | G | 33 | a0001c0001t0001g0017a0001c0011t0001g0071a0002c0003t0002g0029others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1701+6791A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113543709 | ||||||
| chr9:113544299
|
G | GT | 14 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0144others(11): Show | 14 | HG00621.hp2 HG02109.hp1 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.1701+7397dupT | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113544299 | |||||
| chr9:113544299
|
GT | G | 20 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(17): Show | 20 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.1701+7397delT | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113544299 | |||||
| chr9:113544501
|
T | G | 1 | a0001c0001t0001g0024 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1701+7583T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113544501 | ||||||
| chr9:113544537
|
C | T | 32 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1701+7619C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113544537 | ||||||
| chr9:113544788
|
C | G | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1701+7870C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113544788 | ||||||
| chr9:113544789
|
C | G | 1 | a0002c0004t0006g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1701+7871C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113544789 | ||||||
| chr9:113544933
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1701+8015A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113544933 | ||||||
| chr9:113545318
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1701+8400C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113545318 | ||||||
| chr9:113545402
|
T | C | 1 | a0001c0001t0001g0128 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1701+8484T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113545402 | ||||||
| chr9:113545424
|
C | G | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1701+8506C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113545424 | ||||||
| chr9:113545442
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1701+8524C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113545442 | ||||||
| chr9:113545444
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1701+8526T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113545444 | ||||||
| chr9:113545477
|
C | T | 12 | a0001c0001t0002g0067a0001c0001t0003g0026a0001c0001t0003g0038others(9): Show | 12 | HG01081.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1701+8559C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113545477 | ||||||
| chr9:113545790
|
A | G | 1 | a0001c0002t0001g0079 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1701+8872A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113545790 | ||||||
| chr9:113546053
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1701+9135A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113546053 | ||||||
| chr9:113546429
|
G | T | 19 | a0001c0001t0001g0008a0001c0001t0001g0064a0001c0001t0001g0072others(16): Show | 19 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.1701+9511G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113546429 | ||||||
| chr9:113546520
|
C | T | 12 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(9): Show | 12 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.1701+9602C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113546520 | ||||||
| chr9:113546826
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1701+9908C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113546826 | ||||||
| chr9:113546990
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1701+10072C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113546990 | ||||||
| chr9:113547138
|
G | T | 31 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(28): Show | 31 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.1701+10220G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113547138 | ||||||
| chr9:113547434
|
G | A | 5 | a0001c0007t0001g0081a0001c0007t0001g0087a0001c0007t0001g0114others(2): Show | 5 | HG00738.hp2 HG01070.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.1701+10516G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113547434 | ||||||
| chr9:113547493
|
G | A | 32 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1701+10575G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113547493 | ||||||
| chr9:113547606
|
A | G | 7 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(4): Show | 7 | HG02132.hp1 HG02148.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1701+10688A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113547606 | ||||||
| chr9:113547813
|
T | C | 1 | a0006c0012t0002g0016 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1701+10895T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113547813 | ||||||
| chr9:113548713
|
C | T | 32 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1701+11795C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113548713 | ||||||
| chr9:113548795
|
C | T | 30 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(27): Show | 30 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.1701+11877C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113548795 | ||||||
| chr9:113548887
|
G | C | 1 | a0001c0001t0001g0104 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1701+11969G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113548887 | ||||||
| chr9:113548957
|
C | T | 1 | a0001c0001t0004g0004 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1701+12039C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113548957 | ||||||
| chr9:113548978
|
C | T | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1701+12060C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113548978 | ||||||
| chr9:113549111
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1701+12193C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113549111 | ||||||
| chr9:113549469
|
C | CT | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1701+12560dupT | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113549469 | |||||
| chr9:113550054
|
A | G | 1 | a0001c0006t0001g0089 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1701+13136A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113550054 | ||||||
| chr9:113550058
|
C | A | 11 | a0001c0001t0001g0105a0001c0001t0001g0116a0001c0001t0001g0123others(8): Show | 11 | HG00735.hp1 HG00738.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.1701+13140C>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113550058 | ||||||
| chr9:113550058
|
C | T | 14 | a0001c0001t0001g0050a0001c0001t0001g0085a0001c0001t0001g0090others(11): Show | 14 | HG00140.hp1 HG00621.hp1 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.1701+13140C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113550058 | ||||||
| chr9:113550089
|
C | T | 1 | a0001c0002t0001g0051 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1701+13171C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113550089 | ||||||
| chr9:113550229
|
G | A | 1 | a0001c0011t0001g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1701+13311G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113550229 | ||||||
| chr9:113550918
|
T | A | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1701+14000T>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113550918 | ||||||
| chr9:113551017
|
A | C | 2 | a0001c0018t0001g0139a0001c0019t0001g0092 | 2 | HG02055.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1701+14099A>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113551017 | ||||||
| chr9:113551074
|
T | C | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1701+14156T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113551074 | ||||||
| chr9:113551302
|
A | C | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1701+14384A>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113551302 | ||||||
| chr9:113551356
|
G | A | 1 | a0001c0001t0003g0157 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1701+14438G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113551356 | ||||||
| chr9:113551665
|
A | G | 3 | a0002c0003t0002g0031a0002c0003t0002g0074a0002c0003t0002g0076 | 3 | HG01099.hp2 HG01106.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1701+14747A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113551665 | ||||||
| chr9:113551686
|
TAAC | T | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1701+14786_1701+14 others(9): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113551686 | |||||
| chr9:113551955
|
T | A | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1701+15037T>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113551955 | ||||||
| chr9:113552074
|
C | A | 1 | a0001c0001t0001g0043 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1701+15156C>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113552074 | ||||||
| chr9:113552157
|
T | G | 1 | a0001c0013t0001g0142 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1701+15239T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113552157 | ||||||
| chr9:113552163
|
A | G | 1 | a0001c0013t0001g0142 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1701+15245A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113552163 | ||||||
| chr9:113552343
|
G | A | 1 | a0001c0018t0001g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1701+15425G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113552343 | ||||||
| chr9:113552638
|
G | C | 72 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0039others(69): Show | 72 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.1701+15720G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113552638 | ||||||
| chr9:113552838
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1701+15920A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113552838 | ||||||
| chr9:113552919
|
G | T | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1701+16001G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113552919 | ||||||
| chr9:113552941
|
T | G | 1 | a0002c0008t0006g0033 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1701+16023T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113552941 | ||||||
| chr9:113553277
|
A | T | 2 | a0002c0008t0006g0033a0002c0008t0006g0034 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1701+16359A>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113553277 | ||||||
| chr9:113553441
|
T | TAAA | 6 | a0001c0001t0001g0091a0001c0001t0001g0101a0001c0001t0001g0130others(3): Show | 6 | HG00558.hp2 HG02040.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.1701+16540_1701+16 others(9): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553441 | |||||
| chr9:113553441
|
T | TAAAA | 12 | a0001c0001t0001g0043a0001c0001t0001g0065a0001c0001t0001g0082others(9): Show | 12 | HG00408.hp2 HG01109.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.1701+16539_1701+16 others(10): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553441 | |||||
| chr9:113553441
|
T | TAAAAA | 12 | a0001c0001t0001g0049a0001c0001t0001g0064a0001c0001t0001g0108others(9): Show | 12 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(9): Show |
intron_variant | MODIFIER | c.1701+16538_1701+16 others(11): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553441 | |||||
| chr9:113553441
|
T | TAAAAAA | 10 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0110others(7): Show | 10 | HG00140.hp2 HG01258.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1701+16537_1701+16 others(12): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553441 | |||||
| chr9:113553441
|
T | TAAAAAAA | 23 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0072others(20): Show | 23 | HG00639.hp2 HG00735.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.1701+16536_1701+16 others(13): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553441 | |||||
| chr9:113553441
|
T | TAAAAAAA others(1): Show |
10 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0042others(7): Show | 10 | HG01928.hp2 HG02109.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.1701+16535_1701+16 others(14): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553441 | |||||
| chr9:113553441
|
T | TAAAAAAA others(2): Show |
14 | a0001c0001t0001g0080a0001c0001t0001g0134a0001c0001t0001g0141others(11): Show | 14 | HG01109.hp2 HG01981.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.1701+16534_1701+16 others(15): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553441 | |||||
| chr9:113553441
|
T | TAAAAAAA others(3): Show |
6 | a0001c0001t0001g0116a0001c0001t0003g0066a0001c0001t0003g0069others(3): Show | 6 | HG01517.hp1 HG02132.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.1701+16533_1701+16 others(16): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553441 | |||||
| chr9:113553441
|
T | TAAAAAAA others(5): Show |
1 | a0001c0001t0004g0005 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1701+16531_1701+16 others(18): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553441 | |||||
| chr9:113553441
|
T | TAAAAAAA others(6): Show |
1 | a0001c0001t0001g0118 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1701+16530_1701+16 others(19): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553441 | |||||
| chr9:113553441
|
T | TAAAAAAA others(7): Show |
1 | a0001c0001t0001g0050 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1701+16529_1701+16 others(20): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553441 | |||||
| chr9:113553453
|
AAAAAAAA others(3): Show |
A | 2 | a0002c0004t0002g0073a0002c0004t0002g0098 | 2 | NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1701+16537_1701+16 others(16): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553453 | |||||
| chr9:113553453
|
AAAAAAAA others(5): Show |
A | 1 | a0002c0004t0002g0097 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1701+16537_1701+16 others(18): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553453 | |||||
| chr9:113553453
|
AAAAAAAA others(7): Show |
A | 4 | a0002c0004t0002g0094a0002c0004t0002g0096a0002c0005t0008g0015others(1): Show | 4 | HG01243.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1701+16537_1701+16 others(20): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553453 | |||||
| chr9:113553454
|
AAAAAAAT others(4): Show |
A | 2 | a0002c0003t0002g0077a0002c0003t0002g0078 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1701+16538_1701+16 others(17): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553454 | |||||
| chr9:113553454
|
AAAAAAAT others(6): Show |
A | 12 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(9): Show | 12 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.1701+16538_1701+16 others(19): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553454 | |||||
| chr9:113553455
|
AAAAAATA others(5): Show |
A | 1 | a0002c0004t0002g0095 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1701+16539_1701+16 others(18): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553455 | |||||
| chr9:113553456
|
AAAAATAT others(4): Show |
A | 1 | a0001c0011t0001g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1701+16540_1701+16 others(17): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553456 | |||||
| chr9:113553456
|
AAAAATAT others(6): Show |
A | 1 | a0002c0008t0006g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1701+16540_1701+16 others(19): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553456 | |||||
| chr9:113553456
|
AAAAATAT others(8): Show |
A | 4 | a0002c0005t0002g0013a0002c0005t0002g0014a0002c0005t0003g0010others(1): Show | 4 | HG02970.hp2 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1701+16540_1701+16 others(21): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553456 | |||||
| chr9:113553458
|
AAATATAT others(6): Show |
A | 1 | a0002c0008t0006g0033 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1701+16542_1701+16 others(19): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553458 | |||||
| chr9:113553458
|
AAATATAT others(8): Show |
A | 4 | a0002c0004t0006g0018a0002c0004t0006g0023a0002c0005t0002g0009others(1): Show | 4 | HG01978.hp2 HG02280.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1701+16542_1701+16 others(21): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553458 | |||||
| chr9:113553459
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0001g0133 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1701+16542_1701+16 others(18): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553459 | |||||
| chr9:113553459
|
A | AAAAAAAA others(4): Show |
1 | a0001c0001t0004g0003 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1701+16542_1701+16 others(17): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553459 | |||||
| chr9:113553459
|
A | AAAAAAAA others(8): Show |
2 | a0001c0001t0001g0090a0001c0001t0001g0152 | 2 | HG00621.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1701+16542_1701+16 others(21): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553459 | |||||
| chr9:113553459
|
A | AAAAAAAA others(3): Show |
1 | a0001c0006t0001g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1701+16542_1701+16 others(16): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553459 | |||||
| chr9:113553459
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0001g0086 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1701+16542_1701+16 others(18): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553459 | |||||
| chr9:113553459
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0001g0151 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1701+16542_1701+16 others(20): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553459 | |||||
| chr9:113553459
|
A | AAAAAAAA others(2): Show |
5 | a0001c0001t0001g0061a0001c0001t0001g0088a0001c0001t0003g0045others(2): Show | 5 | HG00544.hp2 HG00735.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1701+16542_1701+16 others(15): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553459 | |||||
| chr9:113553459
|
A | AAAAAAAA others(4): Show |
1 | a0001c0002t0001g0126 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1701+16542_1701+16 others(17): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553459 | |||||
| chr9:113553459
|
A | AAAAAAAA others(8): Show |
1 | a0001c0001t0001g0119 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1701+16542_1701+16 others(21): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553459 | |||||
| chr9:113553459
|
A | AAAAAAAA others(5): Show |
1 | a0003c0020t0001g0048 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1701+16542_1701+16 others(18): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553459 | |||||
| chr9:113553459
|
A | AAAAAATA others(3): Show |
3 | a0001c0001t0001g0149a0001c0002t0001g0160a0001c0002t0007g0164 | 3 | HG01975.hp1 NA18994.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1701+16542_1701+16 others(16): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553459 | |||||
| chr9:113553459
|
A | AAAAAATA others(5): Show |
1 | a0001c0002t0001g0051 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1701+16542_1701+16 others(18): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553459 | |||||
| chr9:113553459
|
AAT | A | 5 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0002t0001g0112others(2): Show | 5 | HG01516.hp1 HG02109.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1701+16572_1701+16 others(8): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113553459 | |||||
| chr9:113553460
|
ATATATAT others(8): Show |
A | 1 | a0001c0001t0001g0017 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1701+16543_1701+16 others(21): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113553460 | ||||||
| chr9:113553461
|
T | A | 78 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0039others(75): Show | 78 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.1701+16543T>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113553461 | ||||||
| chr9:113553463
|
T | A | 49 | a0001c0001t0001g0024a0001c0001t0001g0039a0001c0001t0001g0050others(46): Show | 49 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.1701+16545T>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113553463 | ||||||
| chr9:113553465
|
T | A | 20 | a0001c0001t0001g0024a0001c0001t0001g0050a0001c0001t0001g0100others(17): Show | 20 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.1701+16547T>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113553465 | ||||||
| chr9:113553467
|
T | A | 10 | a0001c0001t0001g0100a0001c0001t0001g0110a0001c0001t0001g0111others(7): Show | 10 | HG00544.hp1 HG00621.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1701+16549T>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113553467 | ||||||
| chr9:113554120
|
A | G | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1701+17202A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113554120 | ||||||
| chr9:113554219
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1701+17301T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113554219 | ||||||
| chr9:113554450
|
C | T | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1701+17532C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113554450 | ||||||
| chr9:113554587
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1701+17669G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113554587 | ||||||
| chr9:113554822
|
CT | C | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1701+17911delT | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113554822 | |||||
| chr9:113554926
|
C | G | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1701+18008C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113554926 | ||||||
| chr9:113555472
|
A | AT | 29 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(26): Show | 29 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.1701+18566dupT | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113555472 | |||||
| chr9:113555901
|
G | A | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1701+18983G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113555901 | ||||||
| chr9:113556172
|
A | T | 1 | a0001c0007t0001g0114 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1701+19254A>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113556172 | ||||||
| chr9:113556316
|
C | A | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1701+19398C>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113556316 | ||||||
| chr9:113556436
|
G | A | 1 | a0001c0018t0001g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1701+19518G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113556436 | ||||||
| chr9:113556638
|
G | A | 1 | a0001c0001t0002g0057 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1701+19720G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113556638 | ||||||
| chr9:113557380
|
A | G | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1701+20462A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113557380 | ||||||
| chr9:113557514
|
T | C | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1701+20596T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113557514 | ||||||
| chr9:113557601
|
T | A | 1 | a0002c0004t0002g0094 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1701+20683T>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113557601 | ||||||
| chr9:113557637
|
C | T | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1701+20719C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113557637 | ||||||
| chr9:113557801
|
G | A | 1 | a0001c0018t0001g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1701+20883G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113557801 | ||||||
| chr9:113557827
|
TA | T | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1701+20911delA | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113557827 | |||||
| chr9:113558033
|
A | C | 1 | a0001c0011t0001g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1701+21115A>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113558033 | ||||||
| chr9:113558376
|
G | A | 2 | a0002c0005t0002g0009a0002c0005t0002g0012 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1701+21458G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113558376 | ||||||
| chr9:113558423
|
A | C | 1 | a0001c0001t0001g0084 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1701+21505A>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113558423 | ||||||
| chr9:113558542
|
G | A | 2 | a0001c0018t0001g0139a0001c0019t0001g0092 | 2 | HG02055.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1701+21624G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113558542 | ||||||
| chr9:113558611
|
T | G | 7 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(4): Show | 7 | HG01243.hp1 HG02572.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1701+21693T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113558611 | ||||||
| chr9:113558910
|
C | T | 1 | a0001c0002t0001g0126 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1701+21992C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113558910 | ||||||
| chr9:113558995
|
G | A | 1 | a0002c0005t0008g0015 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1701+22077G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113558995 | ||||||
| chr9:113559025
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1701+22107C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113559025 | ||||||
| chr9:113559064
|
C | G | 1 | a0001c0002t0001g0040 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1701+22146C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113559064 | ||||||
| chr9:113559323
|
C | T | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1701+22405C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113559323 | ||||||
| chr9:113559377
|
T | C | 39 | a0001c0001t0001g0017a0001c0001t0004g0001a0001c0001t0004g0002others(36): Show | 39 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1701+22459T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113559377 | ||||||
| chr9:113559415
|
G | A | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1701+22497G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113559415 | ||||||
| chr9:113559564
|
A | G | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1701+22646A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113559564 | ||||||
| chr9:113559565
|
T | A | 19 | a0001c0001t0001g0042a0001c0001t0001g0151a0001c0001t0001g0152others(16): Show | 19 | HG00544.hp1 HG00558.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1701+22647T>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113559565 | ||||||
| chr9:113559700
|
G | A | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1701+22782G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113559700 | ||||||
| chr9:113559798
|
C | T | 11 | a0001c0001t0001g0105a0001c0001t0001g0116a0001c0001t0001g0123others(8): Show | 11 | HG00735.hp1 HG00738.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.1701+22880C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113559798 | ||||||
| chr9:113559842
|
T | G | 1 | a0001c0011t0001g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1701+22924T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113559842 | ||||||
| chr9:113560172
|
A | T | 1 | a0001c0002t0001g0093 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1701+23254A>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113560172 | ||||||
| chr9:113560386
|
C | T | 4 | a0002c0005t0002g0013a0002c0005t0002g0014a0002c0005t0003g0010others(1): Show | 4 | HG02970.hp2 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1702-23064C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113560386 | ||||||
| chr9:113560394
|
C | T | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1702-23056C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113560394 | ||||||
| chr9:113560506
|
C | T | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1702-22944C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113560506 | ||||||
| chr9:113560700
|
A | G | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1702-22750A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113560700 | ||||||
| chr9:113560793
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1702-22657A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113560793 | ||||||
| chr9:113560963
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1702-22487T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113560963 | ||||||
| chr9:113561054
|
T | C | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1702-22396T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113561054 | ||||||
| chr9:113561223
|
C | T | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1702-22227C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113561223 | ||||||
| chr9:113561400
|
GTCTC | G | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1702-22036_1702-22 others(10): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113561400 | |||||
| chr9:113561432
|
C | T | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1702-22018C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113561432 | ||||||
| chr9:113561455
|
C | T | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1702-21995C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113561455 | ||||||
| chr9:113561586
|
A | ATTT | 19 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(16): Show | 19 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.1702-21850_1702-21 others(9): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113561586 | |||||
| chr9:113561586
|
A | ATTTT | 14 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(11): Show | 14 | HG01243.hp1 HG02280.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.1702-21851_1702-21 others(10): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113561586 | |||||
| chr9:113561634
|
C | G | 13 | a0001c0001t0001g0042a0001c0001t0001g0151a0001c0001t0001g0152others(10): Show | 13 | HG00544.hp1 HG00558.hp1 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.1702-21816C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113561634 | ||||||
| chr9:113561856
|
C | G | 1 | a0001c0002t0001g0007 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1702-21594C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113561856 | ||||||
| chr9:113562294
|
G | A | 1 | a0002c0003t0002g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1702-21156G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113562294 | ||||||
| chr9:113562345
|
C | T | 1 | a0001c0001t0004g0004 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1702-21105C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113562345 | ||||||
| chr9:113562429
|
A | G | 7 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(4): Show | 7 | HG01243.hp1 HG02572.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1702-21021A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113562429 | ||||||
| chr9:113562431
|
C | T | 1 | a0002c0003t0002g0077 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1702-21019C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113562431 | ||||||
| chr9:113562476
|
C | CA | 10 | a0001c0002t0001g0103a0001c0015t0001g0136a0001c0019t0001g0092others(7): Show | 10 | HG00738.hp1 HG01123.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1702-20955dupA | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113562476 | |||||
| chr9:113562476
|
C | CAA | 18 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(15): Show | 18 | HG00140.hp1 HG00741.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.1702-20956_1702-20 others(8): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113562476 | |||||
| chr9:113562685
|
C | G | 3 | a0001c0001t0001g0144a0001c0002t0001g0146a0001c0002t0001g0147 | 3 | HG01109.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1702-20765C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113562685 | ||||||
| chr9:113563130
|
G | C | 19 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(16): Show | 19 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.1702-20320G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113563130 | ||||||
| chr9:113563219
|
C | T | 39 | a0001c0001t0001g0017a0001c0001t0004g0001a0001c0001t0004g0002others(36): Show | 39 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1702-20231C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113563219 | ||||||
| chr9:113563612
|
G | C | 34 | a0001c0001t0001g0017a0001c0011t0001g0071a0002c0003t0002g0029others(31): Show | 34 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1702-19838G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113563612 | ||||||
| chr9:113563825
|
TAGAC | T | 2 | a0002c0005t0002g0009a0002c0005t0002g0012 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1702-19622_1702-19 others(10): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113563825 | |||||
| chr9:113563931
|
G | A | 2 | a0001c0001t0002g0058a0001c0001t0002g0062 | 2 | HG00639.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1702-19519G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113563931 | ||||||
| chr9:113563999
|
T | C | 1 | a0001c0011t0001g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1702-19451T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113563999 | ||||||
| chr9:113564596
|
C | T | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1702-18854C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113564596 | ||||||
| chr9:113564608
|
T | C | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1702-18842T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113564608 | ||||||
| chr9:113564698
|
T | C | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1702-18752T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113564698 | ||||||
| chr9:113564819
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1702-18631G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113564819 | ||||||
| chr9:113564842
|
C | T | 19 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(16): Show | 19 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.1702-18608C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113564842 | ||||||
| chr9:113564850
|
G | T | 2 | a0001c0018t0001g0139a0001c0019t0001g0092 | 2 | HG02055.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1702-18600G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113564850 | ||||||
| chr9:113564858
|
G | C | 1 | a0001c0001t0001g0159 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1702-18592G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113564858 | ||||||
| chr9:113564861
|
C | G | 1 | a0001c0001t0001g0102 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1702-18589C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113564861 | ||||||
| chr9:113564879
|
C | T | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1702-18571C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113564879 | ||||||
| chr9:113564998
|
C | T | 2 | a0001c0001t0001g0047a0003c0020t0001g0048 | 2 | HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1702-18452C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113564998 | ||||||
| chr9:113565180
|
C | T | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1702-18270C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113565180 | ||||||
| chr9:113565411
|
T | TAGG | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1702-18028_1702-18 others(9): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113565411 | |||||
| chr9:113565437
|
A | C | 1 | a0001c0001t0001g0166 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1702-18013A>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113565437 | ||||||
| chr9:113565690
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1702-17760G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113565690 | ||||||
| chr9:113565773
|
A | G | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1702-17677A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113565773 | ||||||
| chr9:113565875
|
C | CTG | 43 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(40): Show | 43 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.1702-17535_1702-17 others(8): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113565875 | |||||
| chr9:113565875
|
C | CTGTG | 21 | a0001c0001t0001g0039a0001c0001t0001g0080a0001c0001t0001g0133others(18): Show | 21 | HG00408.hp1 HG00558.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1702-17537_1702-17 others(10): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113565875 | |||||
| chr9:113565875
|
C | CTGTGTG | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0061others(2): Show | 5 | HG02717.hp1 HG03239.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.1702-17539_1702-17 others(12): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113565875 | |||||
| chr9:113565875
|
C | CTGTGTGT others(1): Show |
3 | a0001c0001t0001g0140a0001c0001t0004g0003a0001c0001t0004g0005 | 3 | HG00639.hp2 NA18957.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1702-17541_1702-17 others(14): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113565875 | |||||
| chr9:113565875
|
C | CTGTGTGT others(3): Show |
1 | a0001c0001t0001g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1702-17543_1702-17 others(16): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113565875 | |||||
| chr9:113565875
|
CTG | C | 4 | a0001c0001t0001g0082a0001c0001t0001g0131a0002c0004t0006g0018others(1): Show | 4 | HG01928.hp1 HG01978.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1702-17535_1702-17 others(8): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113565875 | |||||
| chr9:113565913
|
G | C | 18 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(15): Show | 18 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1702-17537G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113565913 | ||||||
| chr9:113565913
|
G | GTGTC | 5 | a0001c0001t0003g0056a0002c0004t0002g0073a0002c0004t0002g0097others(2): Show | 5 | HG06807.hp2 NA18522.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.1702-17519_1702-17 others(10): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113565913 | |||||
| chr9:113565913
|
G | GTGTGTCT others(3): Show |
1 | a0002c0014t0002g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1702-17534_1702-17 others(16): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113565913 | |||||
| chr9:113565913
|
G | GTGTGTGT others(1): Show |
5 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1702-17534_1702-17 others(14): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113565913 | |||||
| chr9:113565913
|
G | GTGTGTGT others(5): Show |
2 | a0002c0004t0002g0094a0002c0004t0002g0096 | 2 | HG01243.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1702-17534_1702-17 others(18): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113565913 | |||||
| chr9:113565913
|
G | GTGTGTGT others(3): Show |
1 | a0002c0005t0008g0015 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1702-17534_1702-17 others(16): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113565913 | |||||
| chr9:113565913
|
GTGTC | G | 2 | a0001c0001t0001g0024a0001c0019t0001g0092 | 2 | HG02698.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1702-17519_1702-17 others(10): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113565913 | |||||
| chr9:113565915
|
GTC | G | 11 | a0001c0001t0001g0072a0001c0001t0001g0101a0001c0001t0001g0102others(8): Show | 11 | HG00408.hp2 HG00558.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.1702-17533_1702-17 others(8): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113565915 | |||||
| chr9:113565917
|
C | G | 85 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0039others(82): Show | 85 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1702-17533C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113565917 | ||||||
| chr9:113566343
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1702-17107G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113566343 | ||||||
| chr9:113566608
|
A | G | 1 | a0001c0002t0001g0025 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1702-16842A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113566608 | ||||||
| chr9:113566670
|
T | C | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1702-16780T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113566670 | ||||||
| chr9:113566771
|
G | A | 1 | a0001c0002t0001g0160 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1702-16679G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113566771 | ||||||
| chr9:113566844
|
T | C | 32 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1702-16606T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113566844 | ||||||
| chr9:113567128
|
A | G | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1702-16322A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113567128 | ||||||
| chr9:113567164
|
T | C | 2 | a0002c0003t0002g0077a0002c0003t0002g0078 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1702-16286T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113567164 | ||||||
| chr9:113567248
|
C | T | 2 | a0001c0018t0001g0139a0001c0019t0001g0092 | 2 | HG02055.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1702-16202C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113567248 | ||||||
| chr9:113567428
|
G | A | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1702-16022G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113567428 | ||||||
| chr9:113567497
|
C | T | 2 | a0002c0004t0006g0018a0002c0004t0006g0023 | 2 | HG01978.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1702-15953C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113567497 | ||||||
| chr9:113567706
|
T | C | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1702-15744T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113567706 | ||||||
| chr9:113567741
|
A | G | 2 | a0002c0008t0006g0033a0002c0008t0006g0034 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1702-15709A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113567741 | ||||||
| chr9:113567753
|
T | G | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1702-15697T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113567753 | ||||||
| chr9:113567851
|
G | A | 1 | a0003c0020t0001g0048 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1702-15599G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113567851 | ||||||
| chr9:113567923
|
A | G | 1 | a0001c0001t0001g0155 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1702-15527A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113567923 | ||||||
| chr9:113567948
|
T | A | 1 | a0001c0002t0007g0164 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1702-15502T>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113567948 | ||||||
| chr9:113567973
|
T | C | 1 | a0002c0014t0002g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1702-15477T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113567973 | ||||||
| chr9:113568093
|
A | C | 7 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(4): Show | 7 | HG01243.hp1 HG02572.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1702-15357A>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113568093 | ||||||
| chr9:113568235
|
T | C | 1 | a0001c0015t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1702-15215T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113568235 | ||||||
| chr9:113568464
|
A | T | 14 | a0001c0001t0001g0042a0001c0001t0001g0149a0001c0001t0001g0151others(11): Show | 14 | HG00544.hp1 HG00558.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.1702-14986A>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113568464 | ||||||
| chr9:113568472
|
A | C | 1 | a0001c0001t0001g0085 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1702-14978A>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113568472 | ||||||
| chr9:113568609
|
C | T | 2 | a0002c0005t0003g0010a0002c0005t0003g0011 | 2 | HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1702-14841C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113568609 | ||||||
| chr9:113568652
|
C | T | 33 | a0001c0001t0001g0017a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1702-14798C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113568652 | ||||||
| chr9:113568690
|
A | G | 43 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0004g0001others(40): Show | 43 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.1702-14760A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113568690 | ||||||
| chr9:113568942
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1702-14508C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113568942 | ||||||
| chr9:113569013
|
C | T | 2 | a0001c0001t0001g0049a0001c0002t0001g0146 | 2 | HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1702-14437C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113569013 | ||||||
| chr9:113569036
|
G | A | 1 | a0002c0003t0002g0029 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1702-14414G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113569036 | ||||||
| chr9:113569061
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1702-14389C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113569061 | ||||||
| chr9:113569062
|
T | C | 1 | a0001c0001t0001g0152 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1702-14388T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113569062 | ||||||
| chr9:113569063
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1702-14387C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113569063 | ||||||
| chr9:113569124
|
G | C | 1 | a0001c0001t0001g0152 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1702-14326G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113569124 | ||||||
| chr9:113569125
|
C | G | 1 | a0001c0001t0001g0152 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1702-14325C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113569125 | ||||||
| chr9:113569267
|
C | T | 2 | a0001c0001t0001g0050a0004c0009t0001g0121 | 2 | NA18959.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1702-14183C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113569267 | ||||||
| chr9:113569384
|
C | A | 1 | a0001c0001t0001g0085 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1702-14066C>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113569384 | ||||||
| chr9:113569567
|
G | GTCTTTCC others(1): Show |
2 | a0002c0003t0002g0078a0002c0004t0002g0098 | 2 | HG01884.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1702-13872_1702-13 others(14): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113569567 | |||||
| chr9:113569578
|
T | TTTCC | 25 | a0001c0001t0001g0043a0001c0001t0001g0054a0001c0001t0001g0061others(22): Show | 25 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(22): Show |
intron_variant | MODIFIER | c.1702-13811_1702-13 others(10): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113569578 | |||||
| chr9:113569578
|
T | TTTCCTTC others(1): Show |
24 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0027others(21): Show | 24 | HG00621.hp2 HG01123.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.1702-13815_1702-13 others(14): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113569578 | |||||
| chr9:113569578
|
T | TTTCCTTC others(5): Show |
15 | a0001c0001t0001g0047a0001c0001t0001g0082a0001c0001t0001g0086others(12): Show | 15 | HG00639.hp2 HG01070.hp2 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.1702-13819_1702-13 others(18): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113569578 | |||||
| chr9:113569578
|
T | TTTCCTTC others(9): Show |
13 | a0001c0001t0001g0080a0001c0001t0001g0085a0001c0001t0001g0108others(10): Show | 13 | HG00558.hp2 HG01106.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1702-13823_1702-13 others(22): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113569578 | |||||
| chr9:113569578
|
T | TTTCCTTC others(13): Show |
2 | a0001c0001t0003g0056a0001c0001t0003g0157 | 2 | HG01081.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1702-13827_1702-13 others(26): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113569578 | |||||
| chr9:113569578
|
T | TTTCCTTC others(17): Show |
2 | a0001c0001t0001g0133a0001c0001t0003g0066 | 2 | NA18906.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1702-13831_1702-13 others(30): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113569578 | |||||
| chr9:113569578
|
T | TTTCCTTC others(5): Show |
2 | a0002c0004t0002g0094a0002c0004t0002g0097 | 2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1702-13865_1702-13 others(18): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113569578 | |||||
| chr9:113569578
|
T | TTTCCTTC others(13): Show |
3 | a0002c0004t0002g0095a0002c0004t0002g0096a0002c0005t0002g0009 | 3 | HG01243.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1702-13865_1702-13 others(26): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113569578 | |||||
| chr9:113569578
|
T | TTTCCTTC others(17): Show |
2 | a0002c0005t0002g0013a0002c0005t0008g0015 | 2 | HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1702-13865_1702-13 others(30): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113569578 | |||||
| chr9:113569578
|
T | TTTCCTTC others(21): Show |
2 | a0002c0005t0002g0012a0002c0005t0002g0014 | 2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1702-13865_1702-13 others(34): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113569578 | |||||
| chr9:113569578
|
T | TTTCCTTC others(25): Show |
1 | a0002c0005t0003g0010 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1702-13865_1702-13 others(38): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113569578 | |||||
| chr9:113569578
|
T | TTTCCTTC others(29): Show |
1 | a0002c0005t0003g0011 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1702-13865_1702-13 others(42): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113569578 | |||||
| chr9:113569578
|
TTTCC | T | 22 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0084others(19): Show | 22 | HG00558.hp1 HG01167.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.1702-13811_1702-13 others(10): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113569578 | |||||
| chr9:113569578
|
TTTCCTTC others(1): Show |
T | 14 | a0001c0001t0001g0042a0001c0001t0001g0134a0001c0001t0001g0135others(11): Show | 14 | HG00140.hp1 HG00544.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.1702-13815_1702-13 others(14): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113569578 | |||||
| chr9:113569578
|
TTTCCTTC others(5): Show |
T | 3 | a0001c0001t0004g0002a0001c0002t0001g0112a0001c0019t0001g0092 | 3 | HG02132.hp1 HG02698.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1702-13819_1702-13 others(18): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113569578 | |||||
| chr9:113569578
|
TTTCCTTC others(9): Show |
T | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | NA18962.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1702-13823_1702-13 others(22): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113569578 | |||||
| chr9:113569578
|
TTTCCTTC others(13): Show |
T | 1 | a0005c0017t0001g0083 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1702-13827_1702-13 others(26): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113569578 | |||||
| chr9:113569578
|
TTTCCTTC others(17): Show |
T | 1 | a0001c0001t0001g0017 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1702-13831_1702-13 others(30): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113569578 | |||||
| chr9:113569582
|
C | CTTCT | 3 | a0002c0003t0002g0029a0002c0003t0002g0032a0002c0003t0002g0077 | 3 | HG02145.hp1 HG03017.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1702-13865_1702-13 others(10): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113569582 | |||||
| chr9:113569586
|
C | T | 10 | a0002c0003t0002g0030a0002c0003t0002g0075a0002c0003t0005g0019others(7): Show | 10 | HG00738.hp1 HG00741.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1702-13864C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113569586 | ||||||
| chr9:113569590
|
C | T | 2 | a0002c0008t0006g0033a0002c0008t0006g0034 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1702-13860C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113569590 | ||||||
| chr9:113569594
|
C | T | 4 | a0002c0003t0002g0031a0002c0003t0002g0074a0002c0003t0002g0076others(1): Show | 4 | HG00140.hp1 HG01099.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.1702-13856C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113569594 | ||||||
| chr9:113569637
|
C | A | 17 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(14): Show | 17 | HG00140.hp1 HG00741.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.1702-13813C>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113569637 | ||||||
| chr9:113569672
|
A | G | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1702-13778A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113569672 | ||||||
| chr9:113569891
|
T | C | 32 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1702-13559T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113569891 | ||||||
| chr9:113569927
|
TC | T | 7 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(4): Show | 7 | HG01243.hp1 HG02572.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1702-13520delC | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113569927 | |||||
| chr9:113569939
|
C | T | 1 | a0002c0014t0002g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1702-13511C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113569939 | ||||||
| chr9:113569943
|
C | A | 1 | a0001c0001t0001g0151 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1702-13507C>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113569943 | ||||||
| chr9:113569962
|
T | A | 137 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0024others(134): Show | 137 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.1702-13488T>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113569962 | ||||||
| chr9:113569967
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1702-13483C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113569967 | ||||||
| chr9:113569977
|
T | C | 1 | a0001c0015t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1702-13473T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113569977 | ||||||
| chr9:113570272
|
G | A | 2 | a0001c0001t0002g0036a0001c0001t0002g0037 | 2 | HG01516.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1702-13178G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113570272 | ||||||
| chr9:113570553
|
A | AG | 41 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(38): Show | 41 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1702-12897_1702-12 others(7): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113570553 | ||||||
| chr9:113570676
|
A | G | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1702-12774A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113570676 | ||||||
| chr9:113570778
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1702-12672C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113570778 | ||||||
| chr9:113570783
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1702-12667C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113570783 | ||||||
| chr9:113570971
|
A | G | 2 | a0001c0001t0003g0026a0001c0001t0003g0157 | 2 | HG01081.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1702-12479A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113570971 | ||||||
| chr9:113571006
|
C | A | 4 | a0001c0002t0001g0051a0001c0002t0001g0093a0001c0002t0001g0138others(1): Show | 4 | HG00735.hp2 HG01081.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1702-12444C>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113571006 | ||||||
| chr9:113571031
|
T | C | 32 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1702-12419T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113571031 | ||||||
| chr9:113571128
|
C | T | 14 | a0001c0001t0001g0042a0001c0001t0001g0149a0001c0001t0001g0151others(11): Show | 14 | HG00544.hp1 HG00558.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.1702-12322C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113571128 | ||||||
| chr9:113571129
|
C | T | 33 | a0001c0006t0001g0089a0002c0003t0002g0029a0002c0003t0002g0030others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1702-12321C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113571129 | ||||||
| chr9:113571234
|
A | G | 32 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1702-12216A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113571234 | ||||||
| chr9:113571320
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1702-12130C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113571320 | ||||||
| chr9:113571495
|
T | C | 1 | a0001c0001t0001g0064 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1702-11955T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113571495 | ||||||
| chr9:113571599
|
G | A | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1702-11851G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113571599 | ||||||
| chr9:113571599
|
G | C | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1702-11851G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113571599 | ||||||
| chr9:113571629
|
G | A | 1 | a0001c0006t0001g0089 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1702-11821G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113571629 | ||||||
| chr9:113571848
|
A | G | 3 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0125 | 3 | HG02109.hp2 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1702-11602A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113571848 | ||||||
| chr9:113571992
|
A | G | 1 | a0002c0008t0006g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1702-11458A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113571992 | ||||||
| chr9:113572007
|
A | G | 32 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1702-11443A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113572007 | ||||||
| chr9:113572056
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1702-11394G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113572056 | ||||||
| chr9:113572064
|
C | T | 1 | a0001c0011t0001g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1702-11386C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113572064 | ||||||
| chr9:113572178
|
C | T | 18 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(15): Show | 18 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1702-11272C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113572178 | ||||||
| chr9:113572226
|
G | T | 3 | a0002c0004t0002g0073a0002c0004t0002g0097a0002c0004t0002g0098 | 3 | HG06807.hp2 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1702-11224G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113572226 | ||||||
| chr9:113572247
|
T | C | 32 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1702-11203T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113572247 | ||||||
| chr9:113572398
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1702-11052G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113572398 | ||||||
| chr9:113572497
|
G | A | 130 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0024others(127): Show | 130 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.1702-10953G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113572497 | ||||||
| chr9:113572557
|
C | T | 1 | a0002c0014t0002g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1702-10893C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113572557 | ||||||
| chr9:113572855
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1702-10595C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113572855 | ||||||
| chr9:113572875
|
C | A | 7 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(4): Show | 7 | HG01243.hp1 HG02572.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1702-10575C>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113572875 | ||||||
| chr9:113572892
|
C | T | 38 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(35): Show | 38 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.1702-10558C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113572892 | ||||||
| chr9:113572912
|
G | T | 1 | a0001c0001t0004g0002 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1702-10538G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113572912 | ||||||
| chr9:113573109
|
T | C | 2 | a0001c0001t0002g0036a0001c0001t0002g0037 | 2 | HG01516.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1702-10341T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113573109 | ||||||
| chr9:113573690
|
G | C | 18 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(15): Show | 18 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1702-9760G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113573690 | ||||||
| chr9:113573755
|
G | A | 40 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(37): Show | 40 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.1702-9695G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113573755 | ||||||
| chr9:113573819
|
C | G | 18 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(15): Show | 18 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1702-9631C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113573819 | ||||||
| chr9:113573884
|
C | T | 7 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(4): Show | 7 | HG01243.hp1 HG02572.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1702-9566C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113573884 | ||||||
| chr9:113573888
|
A | C | 1 | a0001c0001t0004g0006 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1702-9562A>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113573888 | ||||||
| chr9:113574294
|
C | T | 32 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1702-9156C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113574294 | ||||||
| chr9:113574318
|
A | G | 1 | a0001c0002t0001g0138 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1702-9132A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113574318 | ||||||
| chr9:113574502
|
G | A | 32 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1702-8948G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113574502 | ||||||
| chr9:113574730
|
A | G | 2 | a0001c0001t0001g0140a0001c0015t0001g0136 | 2 | HG00639.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1702-8720A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113574730 | ||||||
| chr9:113574738
|
G | A | 1 | a0001c0001t0004g0004 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1702-8712G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113574738 | ||||||
| chr9:113575122
|
C | A | 1 | a0001c0001t0001g0017 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1702-8328C>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113575122 | ||||||
| chr9:113575175
|
T | A | 2 | a0001c0001t0001g0104a0001c0001t0001g0107 | 2 | HG01258.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.1702-8275T>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113575175 | ||||||
| chr9:113575330
|
T | G | 4 | a0002c0005t0002g0013a0002c0005t0002g0014a0002c0005t0003g0010others(1): Show | 4 | HG02970.hp2 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1702-8120T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113575330 | ||||||
| chr9:113575479
|
G | A | 29 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(26): Show | 29 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.1702-7971G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113575479 | ||||||
| chr9:113575577
|
A | G | 2 | a0001c0018t0001g0139a0001c0019t0001g0092 | 2 | HG02055.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1702-7873A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113575577 | ||||||
| chr9:113575616
|
T | C | 2 | a0002c0008t0006g0033a0002c0008t0006g0034 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1702-7834T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113575616 | ||||||
| chr9:113575753
|
C | A | 1 | a0001c0001t0001g0116 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1702-7697C>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113575753 | ||||||
| chr9:113575914
|
T | G | 1 | a0001c0002t0001g0007 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1702-7536T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113575914 | ||||||
| chr9:113575929
|
G | A | 137 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0024others(134): Show | 137 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.1702-7521G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113575929 | ||||||
| chr9:113576014
|
C | T | 1 | a0001c0002t0001g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1702-7436C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113576014 | ||||||
| chr9:113576062
|
T | C | 1 | a0001c0001t0001g0128 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1702-7388T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113576062 | ||||||
| chr9:113576096
|
G | T | 32 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1702-7354G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113576096 | ||||||
| chr9:113576337
|
C | CT | 10 | a0001c0001t0001g0158a0001c0001t0004g0001a0001c0001t0004g0002others(7): Show | 10 | HG02055.hp1 HG02132.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.1702-7100dupT | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113576337 | |||||
| chr9:113576337
|
C | CTT | 20 | a0002c0003t0002g0077a0002c0003t0002g0078a0002c0004t0002g0073others(17): Show | 20 | HG01243.hp1 HG01884.hp2 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.1702-7101_1702-710 others(6): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113576337 | |||||
| chr9:113576337
|
C | CTTT | 12 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(9): Show | 12 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.1702-7102_1702-710 others(7): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113576337 | |||||
| chr9:113576513
|
G | A | 18 | a0001c0001t0001g0008a0001c0001t0001g0064a0001c0001t0001g0072others(15): Show | 18 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.1702-6937G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113576513 | ||||||
| chr9:113576609
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1702-6841C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113576609 | ||||||
| chr9:113576775
|
C | T | 18 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(15): Show | 18 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1702-6675C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113576775 | ||||||
| chr9:113576862
|
C | T | 14 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0080others(11): Show | 14 | HG00544.hp2 HG00621.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.1702-6588C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113576862 | ||||||
| chr9:113576988
|
G | A | 160 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0024others(157): Show | 160 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1702-6462G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113576988 | ||||||
| chr9:113577070
|
G | A | 32 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1702-6380G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113577070 | ||||||
| chr9:113577163
|
T | C | 18 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(15): Show | 18 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1702-6287T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113577163 | ||||||
| chr9:113577597
|
T | G | 3 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0084 | 3 | HG02559.hp1 HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1702-5853T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113577597 | ||||||
| chr9:113577604
|
G | C | 1 | a0001c0001t0001g0017 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1702-5846G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113577604 | ||||||
| chr9:113578046
|
A | G | 38 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(35): Show | 38 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.1702-5404A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113578046 | ||||||
| chr9:113578105
|
G | A | 14 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(11): Show | 14 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.1702-5345G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113578105 | ||||||
| chr9:113578291
|
G | T | 32 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1702-5159G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113578291 | ||||||
| chr9:113578447
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1702-5003T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113578447 | ||||||
| chr9:113578473
|
A | AC | 8 | a0001c0001t0001g0082a0001c0001t0001g0091a0001c0001t0001g0132others(5): Show | 8 | HG00735.hp1 HG00741.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.1702-4975dupC | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113578473 | |||||
| chr9:113578476
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1702-4974G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113578476 | ||||||
| chr9:113578677
|
A | G | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1702-4773A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113578677 | ||||||
| chr9:113578722
|
T | G | 32 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1702-4728T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113578722 | ||||||
| chr9:113578836
|
T | C | 32 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1702-4614T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113578836 | ||||||
| chr9:113579077
|
AC | A | 32 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1702-4366delC | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 113579077 | |||||
| chr9:113579440
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1702-4010C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113579440 | ||||||
| chr9:113579554
|
A | G | 38 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(35): Show | 38 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.1702-3896A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113579554 | ||||||
| chr9:113579653
|
G | A | 2 | a0002c0004t0006g0018a0002c0004t0006g0023 | 2 | HG01978.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1702-3797G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113579653 | ||||||
| chr9:113579865
|
C | G | 1 | a0002c0008t0006g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1702-3585C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113579865 | ||||||
| chr9:113580008
|
C | T | 2 | a0001c0001t0004g0003a0001c0001t0004g0005 | 2 | NA18957.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1702-3442C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113580008 | ||||||
| chr9:113580021
|
G | A | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1702-3429G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113580021 | ||||||
| chr9:113580378
|
C | T | 7 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(4): Show | 7 | HG01243.hp1 HG02572.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1702-3072C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113580378 | ||||||
| chr9:113580664
|
C | T | 1 | a0001c0001t0004g0006 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1702-2786C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113580664 | ||||||
| chr9:113580764
|
G | A | 32 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1702-2686G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113580764 | ||||||
| chr9:113580788
|
C | T | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1702-2662C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113580788 | ||||||
| chr9:113580914
|
C | T | 14 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(11): Show | 14 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.1702-2536C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113580914 | ||||||
| chr9:113580964
|
C | T | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1702-2486C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113580964 | ||||||
| chr9:113581317
|
A | C | 1 | a0001c0001t0001g0027 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1702-2133A>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113581317 | ||||||
| chr9:113581368
|
G | A | 32 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1702-2082G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113581368 | ||||||
| chr9:113581424
|
A | T | 1 | a0001c0001t0001g0100 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1702-2026A>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113581424 | ||||||
| chr9:113581639
|
G | A | 3 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0084 | 3 | HG02559.hp1 HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1702-1811G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113581639 | ||||||
| chr9:113581761
|
G | A | 2 | a0001c0018t0001g0139a0001c0019t0001g0092 | 2 | HG02055.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1702-1689G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113581761 | ||||||
| chr9:113581817
|
C | A | 1 | a0001c0001t0001g0088 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1702-1633C>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113581817 | ||||||
| chr9:113581933
|
G | A | 32 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1702-1517G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113581933 | ||||||
| chr9:113582070
|
A | T | 4 | a0002c0004t0006g0018a0002c0004t0006g0023a0002c0008t0006g0033others(1): Show | 4 | HG01978.hp2 HG02922.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1702-1380A>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113582070 | ||||||
| chr9:113582126
|
A | G | 1 | a0001c0001t0004g0006 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1702-1324A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113582126 | ||||||
| chr9:113582363
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1702-1087T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113582363 | ||||||
| chr9:113582368
|
G | A | 32 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1702-1082G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113582368 | ||||||
| chr9:113582671
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1702-779A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113582671 | ||||||
| chr9:113582989
|
G | A | 3 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0084 | 3 | HG02559.hp1 HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1702-461G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113582989 | ||||||
| chr9:113583191
|
T | C | 32 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1702-259T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113583191 | ||||||
| chr9:113583285
|
C | A | 32 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1702-165C>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 17/22 | chr9 | 113583285 | ||||||
| chr9:113584500
|
TGAG | T | 5 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(2): Show | 5 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.2679+74_2679+76del others(3): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113584500 | ||||||
| chr9:113585127
|
GA | G | 2 | a0002c0008t0006g0033a0002c0008t0006g0034 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2679+702delA | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr9 | 113585127 | |||||
| chr9:113585832
|
A | G | 25 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(22): Show | 25 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.2679+1405A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113585832 | ||||||
| chr9:113585984
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2679+1557G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113585984 | ||||||
| chr9:113586294
|
C | T | 1 | a0001c0011t0001g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2679+1867C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113586294 | ||||||
| chr9:113586310
|
C | G | 1 | a0001c0001t0001g0128 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2679+1883C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113586310 | ||||||
| chr9:113586371
|
A | G | 32 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(29): Show | 32 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.2679+1944A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113586371 | ||||||
| chr9:113586721
|
T | C | 12 | a0001c0001t0001g0042a0001c0001t0001g0149a0001c0001t0001g0151others(9): Show | 12 | HG00544.hp1 HG00558.hp1 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.2679+2294T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113586721 | ||||||
| chr9:113586929
|
G | C | 39 | a0001c0001t0001g0145a0001c0001t0004g0001a0001c0001t0004g0002others(36): Show | 39 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.2679+2502G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113586929 | ||||||
| chr9:113587018
|
G | A | 26 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(23): Show | 26 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.2679+2591G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113587018 | ||||||
| chr9:113587080
|
G | T | 21 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(18): Show | 21 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.2679+2653G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113587080 | ||||||
| chr9:113587158
|
A | G | 74 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0039others(71): Show | 74 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.2679+2731A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113587158 | ||||||
| chr9:113587158
|
A | T | 7 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(4): Show | 7 | HG01243.hp1 HG02572.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2679+2731A>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113587158 | ||||||
| chr9:113587179
|
C | T | 14 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(11): Show | 14 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.2679+2752C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113587179 | ||||||
| chr9:113587421
|
A | C | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2679+2994A>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113587421 | ||||||
| chr9:113587471
|
C | T | 7 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(4): Show | 7 | HG01243.hp1 HG02572.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2679+3044C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113587471 | ||||||
| chr9:113587817
|
C | T | 2 | a0002c0005t0002g0009a0002c0005t0002g0012 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2679+3390C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113587817 | ||||||
| chr9:113587825
|
G | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0158 | 2 | NA18968.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.2679+3398G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113587825 | ||||||
| chr9:113588370
|
C | G | 137 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0024others(134): Show | 137 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.2680-2963C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113588370 | ||||||
| chr9:113588424
|
G | A | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.2680-2909G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113588424 | ||||||
| chr9:113588435
|
A | G | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.2680-2898A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113588435 | ||||||
| chr9:113588676
|
T | G | 2 | a0001c0001t0001g0123a0001c0001t0001g0143 | 2 | HG02040.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2680-2657T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113588676 | ||||||
| chr9:113588749
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2680-2584C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113588749 | ||||||
| chr9:113589355
|
T | C | 1 | a0001c0001t0003g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2680-1978T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113589355 | ||||||
| chr9:113589687
|
G | A | 11 | a0001c0001t0002g0067a0001c0001t0003g0038a0001c0001t0003g0044others(8): Show | 11 | HG01081.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.2680-1646G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113589687 | ||||||
| chr9:113590093
|
C | T | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.2680-1240C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113590093 | ||||||
| chr9:113590182
|
T | C | 1 | a0001c0002t0001g0079 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2680-1151T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113590182 | ||||||
| chr9:113590191
|
T | A | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | NA18957.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.2680-1142T>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113590191 | ||||||
| chr9:113590203
|
T | C | 14 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(11): Show | 14 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.2680-1130T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113590203 | ||||||
| chr9:113590388
|
T | C | 1 | a0001c0002t0001g0093 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2680-945T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113590388 | ||||||
| chr9:113590557
|
T | TATCC | 17 | a0001c0001t0001g0017a0001c0001t0001g0049a0001c0001t0001g0065others(14): Show | 17 | HG01516.hp2 HG01517.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.2680-733_2680-730d others(6): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr9 | 113590557 | |||||
| chr9:113590557
|
T | TATCCATC others(1): Show |
5 | a0001c0001t0004g0002a0002c0003t0002g0029a0002c0003t0002g0075others(2): Show | 5 | HG00738.hp1 HG00741.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.2680-737_2680-730d others(10): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr9 | 113590557 | |||||
| chr9:113590557
|
TATCC | T | 2 | a0001c0001t0001g0135a0001c0015t0001g0136 | 2 | HG00735.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2680-733_2680-730d others(6): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr9 | 113590557 | |||||
| chr9:113590557
|
TATCCATC others(1): Show |
T | 14 | a0002c0004t0002g0094a0002c0004t0002g0095a0002c0004t0002g0096others(11): Show | 14 | HG01243.hp1 HG01978.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.2680-737_2680-730d others(10): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr9 | 113590557 | |||||
| chr9:113590557
|
TATCCATC others(5): Show |
T | 4 | a0002c0004t0002g0073a0002c0004t0002g0097a0002c0004t0002g0098others(1): Show | 4 | HG02809.hp2 HG06807.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2680-741_2680-730d others(14): Show |
RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr9 | 113590557 | |||||
| chr9:113590940
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2680-393A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113590940 | ||||||
| chr9:113591051
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2680-282C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113591051 | ||||||
| chr9:113591082
|
C | T | 71 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0039others(68): Show | 71 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.2680-251C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113591082 | ||||||
| chr9:113591209
|
G | A | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | NA18962.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2680-124G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 18/22 | chr9 | 113591209 | ||||||
| chr9:113591909
|
A | G | 2 | a0002c0005t0002g0009a0002c0005t0002g0012 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2744+512A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 19/22 | chr9 | 113591909 | ||||||
| chr9:113591933
|
A | G | 1 | a0001c0001t0001g0065 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2744+536A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 19/22 | chr9 | 113591933 | ||||||
| chr9:113591993
|
G | C | 14 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(11): Show | 14 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.2744+596G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 19/22 | chr9 | 113591993 | ||||||
| chr9:113592060
|
C | T | 7 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(4): Show | 7 | HG01243.hp1 HG02572.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2744+663C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 19/22 | chr9 | 113592060 | ||||||
| chr9:113592110
|
A | G | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.2744+713A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 19/22 | chr9 | 113592110 | ||||||
| chr9:113592723
|
A | T | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.2744+1326A>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 19/22 | chr9 | 113592723 | ||||||
| chr9:113592945
|
T | C | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.2745-1485T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 19/22 | chr9 | 113592945 | ||||||
| chr9:113593028
|
G | C | 1 | a0001c0002t0001g0137 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2745-1402G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 19/22 | chr9 | 113593028 | ||||||
| chr9:113593083
|
G | T | 1 | a0004c0009t0001g0121 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2745-1347G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 19/22 | chr9 | 113593083 | ||||||
| chr9:113593135
|
G | A | 73 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0039others(70): Show | 73 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.2745-1295G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 19/22 | chr9 | 113593135 | ||||||
| chr9:113593142
|
C | T | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.2745-1288C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 19/22 | chr9 | 113593142 | ||||||
| chr9:113593678
|
G | C | 1 | a0001c0001t0001g0024 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2745-752G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 19/22 | chr9 | 113593678 | ||||||
| chr9:113593830
|
G | A | 1 | a0001c0002t0001g0120 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2745-600G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 19/22 | chr9 | 113593830 | ||||||
| chr9:113593983
|
G | C | 1 | a0002c0003t0005g0021 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2745-447G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 19/22 | chr9 | 113593983 | ||||||
| chr9:113594013
|
C | T | 7 | a0002c0005t0002g0009a0002c0005t0002g0012a0002c0005t0002g0013others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.2745-417C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 19/22 | chr9 | 113594013 | ||||||
| chr9:113594093
|
G | C | 98 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0039others(95): Show | 98 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.2745-337G>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 19/22 | chr9 | 113594093 | ||||||
| chr9:113594109
|
C | T | 3 | a0001c0001t0001g0110a0001c0001t0001g0141a0001c0002t0001g0146 | 3 | HG01981.hp1 HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2745-321C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 19/22 | chr9 | 113594109 | ||||||
| chr9:113594150
|
G | T | 2 | a0001c0018t0001g0139a0001c0019t0001g0092 | 2 | HG02055.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.2745-280G>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 19/22 | chr9 | 113594150 | ||||||
| chr9:113594173
|
G | A | 4 | a0002c0004t0006g0018a0002c0004t0006g0023a0002c0008t0006g0033others(1): Show | 4 | HG01978.hp2 HG02922.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2745-257G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 19/22 | chr9 | 113594173 | ||||||
| chr9:113594187
|
C | T | 1 | a0001c0015t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2745-243C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 19/22 | chr9 | 113594187 | ||||||
| chr9:113594236
|
A | G | 160 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0024others(157): Show | 160 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.2745-194A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 19/22 | chr9 | 113594236 | ||||||
| chr9:113594249
|
C | G | 122 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0024others(119): Show | 122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.2745-181C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 19/22 | chr9 | 113594249 | ||||||
| chr9:113594269
|
C | G | 7 | a0002c0004t0002g0073a0002c0004t0002g0094a0002c0004t0002g0095others(4): Show | 7 | HG01243.hp1 HG02572.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2745-161C>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 19/22 | chr9 | 113594269 | ||||||
| chr9:113594351
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2745-79G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 19/22 | chr9 | 113594351 | ||||||
| chr9:113594555
|
G | A | 1 | a0001c0018t0001g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2846+24G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 20/22 | chr9 | 113594555 | ||||||
| chr9:113594578
|
TC | T | 15 | a0001c0002t0001g0040a0002c0003t0002g0029a0002c0003t0002g0030others(12): Show | 15 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.2846+51delC | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr9 | 113594578 | |||||
| chr9:113594601
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2846+70G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 20/22 | chr9 | 113594601 | ||||||
| chr9:113594795
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2847-124C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 20/22 | chr9 | 113594795 | ||||||
| chr9:113595050
|
G | A | 1 | a0001c0011t0001g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2908+70G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 21/22 | chr9 | 113595050 | ||||||
| chr9:113595128
|
C | T | 107 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0027others(104): Show | 107 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.2908+148C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 21/22 | chr9 | 113595128 | ||||||
| chr9:113595400
|
G | A | 17 | a0001c0001t0002g0067a0002c0004t0002g0073a0002c0004t0002g0094others(14): Show | 17 | HG01243.hp1 HG01978.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.2909-199G>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 21/22 | chr9 | 113595400 | ||||||
| chr9:113595571
|
C | A | 3 | a0002c0004t0002g0073a0002c0004t0002g0097a0002c0004t0002g0098 | 3 | HG06807.hp2 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2909-28C>A | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 21/22 | chr9 | 113595571 | ||||||
| chr9:113595892
|
A | G | 1 | a0001c0001t0004g0002 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3075+127A>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 22/22 | chr9 | 113595892 | ||||||
| chr9:113595972
|
C | T | 3 | a0001c0001t0001g0050a0001c0001t0001g0072a0001c0001t0001g0122 | 3 | HG01167.hp1 NA18959.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.3075+207C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 22/22 | chr9 | 113595972 | ||||||
| chr9:113596005
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3075+240T>C | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 22/22 | chr9 | 113596005 | ||||||
| chr9:113596007
|
C | T | 8 | a0001c0001t0002g0067a0002c0004t0002g0073a0002c0004t0002g0094others(5): Show | 8 | HG01243.hp1 HG02572.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.3075+242C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 22/22 | chr9 | 113596007 | ||||||
| chr9:113596258
|
C | T | 10 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(7): Show | 10 | HG00140.hp1 HG00741.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.3075+493C>T | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 22/22 | chr9 | 113596258 | ||||||
| chr9:113596524
|
T | G | 1 | a0001c0006t0001g0063 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3076-244T>G | RGS3 | ENSG00000138835.24 | transcript | ENST00000695401.1 | protein_coding | 22/22 | chr9 | 113596524 |