Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 57180 |
|---|---|
| ensemblid | ENSG00000133627.18 |
| hgncid | 17256 |
| symbol | ACTR3B |
| name | actin related protein 3B |
| refseq_nuc | NM_020445.6 |
| refseq_prot | NP_065178.1 |
| ensembl_nuc | ENST00000256001.13 |
| ensembl_prot | ENSP00000256001.8 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 152759752 |
| end | 152855378 |
| strand | + |
| ver | v1.2 |
| region | chr7:152759752-152855378 |
| region5000 | chr7:152754752-152860378 |
| regionname0 | ACTR3B_chr7_152759752_152855378 |
| regionname5000 | ACTR3B_chr7_152754752_152860378 |
| 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 | 418 | 309 | 90 | 56 | 119 | 10 | 32 | 89 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| a0002 | 0/0 | 418 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1257 | 303 | 85 | 55 | 119 | 10 | 32 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| c0002 | 0/0 | 1257 | 2 | 2 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| c0003 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| c0004 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| c0005 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| c0006 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| c0007 | 0/0 | 1257 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 957 | 179 | 51 | 39 | 60 | 7 | 20 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| t0002 | 0/0 | 957 | 110 | 25 | 14 | 56 | 3 | 12 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| t0003 | 0/0 | 957 | 8 | 8 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| t0004 | 0/0 | 957 | 3 | 3 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| t0005 | 0/0 | 957 | 2 | 2 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| t0006 | 0/0 | 957 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| t0007 | 0/0 | 957 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| t0008 | 0/0 | 957 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| t0009 | 0/0 | 957 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| t0010 | 0/0 | 957 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| t0011 | 0/0 | 957 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0141 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0225 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1257 | 303 | 85 | 55 | 119 | 10 | 32 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| a0001c0002 | 0/0 | 1257 | 2 | 2 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| a0001c0003 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| a0001c0004 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| a0001c0005 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| a0001c0007 | 0/0 | 1257 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| a0002c0006 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2213 | 173 | 47 | 38 | 59 | 7 | 20 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| a0001c0001t0002 | 0/0 | 2213 | 110 | 25 | 14 | 56 | 3 | 12 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| a0001c0001t0003 | 0/0 | 2213 | 7 | 7 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| a0001c0001t0004 | 0/0 | 2213 | 3 | 3 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| a0001c0001t0005 | 0/0 | 2213 | 2 | 2 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| a0001c0001t0006 | 0/0 | 2213 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| a0001c0001t0007 | 0/0 | 2213 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| a0001c0001t0008 | 0/0 | 2213 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| a0001c0001t0009 | 0/0 | 2213 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| a0001c0001t0010 | 0/0 | 2213 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| a0001c0001t0011 | 0/0 | 2213 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| a0001c0002t0001 | 0/0 | 2213 | 2 | 2 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| a0001c0003t0003 | 0/0 | 2213 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| a0001c0004t0001 | 0/0 | 2213 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| a0001c0005t0001 | 0/0 | 2213 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| a0001c0007t0001 | 0/0 | 2213 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| a0002c0006t0001 | 0/0 | 2213 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | copy fasta | chr7 | 152754752 | 152860378 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0141 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0225 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0006g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0006g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0007g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0007g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0008g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0009g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0010g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0001t0011g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0003t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0004t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0005t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0001c0007t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| a0002c0006t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0070 | EUR | GBR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0253 | EUR | GBR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | CHS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | CHS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | CHS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | CHS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | CHS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0100 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01099 | hp1 | a0001 | c0001 | t0011 | g0164 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01106 | hp1 | a0001 | c0001 | t0010 | g0228 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01192 | hp2 | a0001 | c0007 | t0001 | g0109 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | CLM | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | CLM | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | CLM | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01496 | hp1 | a0001 | c0001 | t0009 | g0142 | AMR | CLM | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | IBS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0068 | EUR | IBS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | IBS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0099 | EUR | IBS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0209 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0179 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0176 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | PEL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PEL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PEL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0105 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | CDX | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | CDX | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02257 | hp1 | a0001 | c0004 | t0001 | g0303 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0168 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PEL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0173 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0211 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0101 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0183 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02965 | hp1 | a0001 | c0001 | t0008 | g0307 | AFR | ESN | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | ESN | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ESN | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ESN | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0169 | AFR | ESN | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0071 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | MSL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ESN | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | ESN | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | ESN | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | ESN | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | MSL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | MSL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0290 | AFR | MSL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | MSL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | MSL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0279 | AFR | MSL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | MSL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0163 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0171 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ESN | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0174 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03579 | hp1 | a0001 | c0003 | t0003 | g0167 | AFR | MSL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0170 | AFR | MSL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0155 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | STU | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | STU | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0157 | SAS | BEB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0087 | SAS | BEB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0072 | SAS | STU | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | STU | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0158 | SAS | STU | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | STU | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | STU | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | STU | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | STU | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | STU | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | YRI | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | YRI | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | YRI | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | YRI | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18948 | hp2 | a0001 | c0001 | t0006 | g0194 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18984 | hp2 | a0002 | c0006 | t0001 | g0189 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19002 | hp2 | a0001 | c0001 | t0006 | g0185 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19010 | hp2 | a0001 | c0001 | t0007 | g0059 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19012 | hp1 | a0001 | c0001 | t0007 | g0041 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | LWK | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0180 | AFR | LWK | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | LWK | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | LWK | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | YRI | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | YRI | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | ASW | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | ASW | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | TSI | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | TSI | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | TSI | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | TSI | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0166 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0286 | AFR | MSL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | MSL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | USA | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | USA | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA20300 | hp1 | a0001 | c0005 | t0001 | g0301 | AFR | USA | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | USA | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | LWK | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | LWK | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0225 | REF | REF | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0141 | REF | REF | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:152823436
|
A | G | 1 | a0002 | 1 | NA18984.hp2 | missense_variant | MODERATE | c.779A>G | p.Asn260Ser | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 8/12 | 910/2213 | 779/1257 | 260/418 | chr7 | 152823436 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:152800631
|
C | T | 1 | a0001c0007 | 1 | HG01192.hp2 | synonymous_variant | LOW | c.201C>T | p.Ile67Ile | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 3/12 | 332/2213 | 201/1257 | 67/418 | chr7 | 152800631 | ||
| chr7:152801683
|
G | A | 1 | a0001c0003 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.288G>A | p.Val96Val | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/12 | 419/2213 | 288/1257 | 96/418 | chr7 | 152801683 | ||
| chr7:152823386
|
C | T | 1 | a0001c0002 | 2 | HG01884.hp1 HG02572.hp1 |
synonymous_variant | LOW | c.729C>T | p.Ala243Ala | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 8/12 | 860/2213 | 729/1257 | 243/418 | chr7 | 152823386 | ||
| chr7:152825098
|
C | T | 1 | a0001c0005 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.927C>T | p.Ile309Ile | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/12 | 1058/2213 | 927/1257 | 309/418 | chr7 | 152825098 | ||
| chr7:152852210
|
A | C | 1 | a0001c0004 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.1036A>C | p.Arg346Arg | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/12 | 1167/2213 | 1036/1257 | 346/418 | chr7 | 152852210 | ||
| chr7:152852239
|
C | T | 1 | a0001c0004 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.1065C>T | p.Gly355Gly | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/12 | 1196/2213 | 1065/1257 | 355/418 | chr7 | 152852239 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:152759774
|
C | T | 3 | a0001c0001t0003a0001c0001t0004a0001c0003t0003 | 11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-109C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/12 | chr7 | 152759774 | ||||||
| chr7:152759809
|
T | C | 1 | a0001c0001t0008 | 1 | HG02965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-74T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/12 | 74 | chr7 | 152759809 | |||||
| chr7:152759824
|
C | T | 6 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(3): Show | 124 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(121): Show |
5_prime_UTR_variant | MODIFIER | c.-59C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/12 | 59 | chr7 | 152759824 | |||||
| chr7:152854681
|
G | A | 1 | a0001c0001t0009 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*128G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 12/12 | 128 | chr7 | 152854681 | |||||
| chr7:152854703
|
C | T | 2 | a0001c0001t0010a0001c0001t0011 | 2 | HG01099.hp1 HG01106.hp1 |
3_prime_UTR_variant | MODIFIER | c.*150C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 12/12 | 150 | chr7 | 152854703 | |||||
| chr7:152854741
|
G | C | 2 | a0001c0001t0005a0001c0001t0008 | 3 | HG02723.hp2 HG02965.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*188G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 12/12 | 188 | chr7 | 152854741 | |||||
| chr7:152854781
|
C | T | 1 | a0001c0001t0006 | 2 | NA18948.hp2 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*228C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 12/12 | 228 | chr7 | 152854781 | |||||
| chr7:152854872
|
A | T | 1 | a0001c0001t0007 | 2 | NA19010.hp2 NA19012.hp1 |
3_prime_UTR_variant | MODIFIER | c.*319A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 12/12 | 319 | chr7 | 152854872 | |||||
| chr7:152854886
|
C | T | 1 | a0001c0001t0004 | 3 | HG01891.hp1 HG02976.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*333C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 12/12 | 333 | chr7 | 152854886 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:152759968
|
C | G | 1 | a0001c0001t0008g0307 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.44+42C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152759968 | ||||||
| chr7:152759971
|
T | C | 2 | a0001c0001t0002g0004a0001c0001t0002g0005 | 2 | NA18939.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.44+45T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152759971 | ||||||
| chr7:152760070
|
G | T | 1 | a0001c0001t0001g0306 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.44+144G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152760070 | ||||||
| chr7:152760104
|
C | A | 1 | a0001c0001t0002g0006 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.44+178C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152760104 | ||||||
| chr7:152760117
|
G | C | 1 | a0001c0001t0002g0007 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.44+191G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152760117 | ||||||
| chr7:152760173
|
G | C | 3 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010 | 3 | NA18988.hp2 NA19054.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.44+247G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152760173 | ||||||
| chr7:152760347
|
C | T | 1 | a0001c0001t0008g0307 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.44+421C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152760347 | ||||||
| chr7:152760457
|
C | CACCT | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.44+534_44+537dupCT others(2): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152760457 | |||||
| chr7:152760457
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.44+531C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152760457 | ||||||
| chr7:152760598
|
A | G | 1 | a0001c0001t0001g0304 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.44+672A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152760598 | ||||||
| chr7:152760630
|
A | G | 6 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(3): Show | 6 | HG01952.hp1 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.44+704A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152760630 | ||||||
| chr7:152760718
|
C | T | 119 | a0001c0001t0001g0003a0001c0001t0001g0184a0001c0001t0001g0186others(116): Show | 120 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.44+792C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152760718 | ||||||
| chr7:152760833
|
G | A | 1 | a0001c0001t0008g0307 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.44+907G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152760833 | ||||||
| chr7:152761060
|
A | G | 1 | a0001c0001t0001g0297 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.44+1134A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152761060 | ||||||
| chr7:152761096
|
G | C | 3 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0018 | 3 | NA18989.hp2 NA19002.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.44+1170G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152761096 | ||||||
| chr7:152761304
|
C | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.44+1378C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152761304 | ||||||
| chr7:152761368
|
T | G | 2 | a0001c0001t0002g0019a0001c0001t0002g0020 | 2 | HG01361.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.44+1442T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152761368 | ||||||
| chr7:152761652
|
CTTAGAAA others(3): Show |
C | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.44+1728_44+1737del others(10): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152761652 | |||||
| chr7:152761661
|
G | A | 18 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.44+1735G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152761661 | ||||||
| chr7:152761663
|
T | A | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.44+1737T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152761663 | ||||||
| chr7:152761698
|
G | A | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.44+1772G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152761698 | ||||||
| chr7:152761730
|
A | G | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.44+1804A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152761730 | ||||||
| chr7:152761768
|
C | T | 8 | a0001c0001t0001g0296a0001c0001t0002g0002a0001c0001t0002g0019others(5): Show | 9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.44+1842C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152761768 | ||||||
| chr7:152761961
|
G | A | 1 | a0001c0001t0002g0021 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.44+2035G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152761961 | ||||||
| chr7:152762062
|
C | T | 8 | a0001c0001t0001g0296a0001c0001t0002g0002a0001c0001t0002g0019others(5): Show | 9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.44+2136C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152762062 | ||||||
| chr7:152762111
|
T | G | 1 | a0001c0001t0001g0022 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.44+2185T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152762111 | ||||||
| chr7:152762345
|
T | C | 1 | a0001c0001t0008g0307 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.44+2419T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152762345 | ||||||
| chr7:152762355
|
C | T | 9 | a0001c0001t0001g0003a0001c0001t0001g0288a0001c0001t0001g0289others(6): Show | 10 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.44+2429C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152762355 | ||||||
| chr7:152762570
|
A | G | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.44+2644A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152762570 | ||||||
| chr7:152762599
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.44+2673A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152762599 | ||||||
| chr7:152762602
|
C | A | 96 | a0001c0001t0001g0200a0001c0001t0002g0004a0001c0001t0002g0005others(93): Show | 96 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.44+2676C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152762602 | ||||||
| chr7:152762928
|
C | T | 4 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106others(1): Show | 4 | HG02055.hp1 HG02965.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.44+3002C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152762928 | ||||||
| chr7:152762956
|
A | G | 7 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(4): Show | 7 | HG01952.hp1 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.44+3030A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152762956 | ||||||
| chr7:152763313
|
C | CA | 85 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022others(82): Show | 86 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.44+3417dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152763313 | |||||
| chr7:152763313
|
CA | C | 74 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(71): Show | 75 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.44+3417delA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152763313 | |||||
| chr7:152763313
|
CAA | C | 14 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(11): Show | 14 | HG01070.hp2 HG01192.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.44+3416_44+3417del others(2): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152763313 | |||||
| chr7:152763313
|
CAAA | C | 13 | a0001c0001t0001g0188a0001c0001t0001g0190a0001c0001t0001g0191others(10): Show | 13 | HG01109.hp1 HG01952.hp2 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.44+3415_44+3417del others(3): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152763313 | |||||
| chr7:152763502
|
C | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.44+3576C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152763502 | ||||||
| chr7:152763703
|
C | T | 11 | a0001c0001t0003g0166a0001c0001t0003g0168a0001c0001t0003g0173others(8): Show | 11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.44+3777C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152763703 | ||||||
| chr7:152763844
|
A | G | 1 | a0001c0001t0002g0100 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.44+3918A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152763844 | ||||||
| chr7:152763978
|
T | G | 1 | a0001c0001t0005g0183 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.44+4052T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152763978 | ||||||
| chr7:152764162
|
C | G | 1 | a0001c0005t0001g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.44+4236C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152764162 | ||||||
| chr7:152764163
|
G | A | 94 | a0001c0001t0001g0003a0001c0001t0001g0201a0001c0001t0001g0202others(91): Show | 95 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.44+4237G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152764163 | ||||||
| chr7:152764319
|
T | C | 1 | a0001c0001t0002g0025 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.44+4393T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152764319 | ||||||
| chr7:152764435
|
C | T | 8 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(5): Show | 8 | HG02486.hp1 HG02717.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.44+4509C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152764435 | ||||||
| chr7:152764562
|
C | T | 9 | a0001c0001t0001g0003a0001c0001t0001g0288a0001c0001t0001g0289others(6): Show | 10 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.44+4636C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152764562 | ||||||
| chr7:152764630
|
C | T | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG00423.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.44+4704C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152764630 | ||||||
| chr7:152764643
|
CA | C | 170 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(167): Show | 172 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.44+4732delA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152764643 | |||||
| chr7:152764666
|
T | G | 1 | a0001c0001t0002g0062 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.44+4740T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152764666 | ||||||
| chr7:152764790
|
C | CA | 8 | a0001c0001t0001g0296a0001c0001t0002g0002a0001c0001t0002g0019others(5): Show | 9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.44+4865dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152764790 | |||||
| chr7:152764806
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.44+4880C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152764806 | ||||||
| chr7:152764849
|
A | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.44+4923A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152764849 | ||||||
| chr7:152764858
|
A | G | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.44+4932A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152764858 | ||||||
| chr7:152765109
|
CT | C | 121 | a0001c0001t0001g0139a0001c0001t0001g0200a0001c0001t0001g0296others(118): Show | 122 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.44+5205delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152765109 | |||||
| chr7:152765127
|
T | TTTC | 15 | a0001c0001t0001g0201a0001c0001t0001g0239a0001c0001t0001g0240others(12): Show | 15 | HG01167.hp2 HG01169.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.44+5203_44+5204ins others(3): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152765127 | |||||
| chr7:152765127
|
T | TTTTC | 97 | a0001c0001t0001g0003a0001c0001t0001g0184a0001c0001t0001g0186others(94): Show | 98 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.44+5204_44+5205ins others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152765127 | |||||
| chr7:152765132
|
C | CTTTTT | 3 | a0001c0001t0001g0238a0001c0001t0001g0267a0001c0001t0001g0292 | 3 | HG01243.hp2 HG02257.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.44+5206_44+5207ins others(5): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152765132 | ||||||
| chr7:152765132
|
C | T | 112 | a0001c0001t0001g0003a0001c0001t0001g0184a0001c0001t0001g0186others(109): Show | 113 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.44+5206C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152765132 | ||||||
| chr7:152765252
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.44+5326G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152765252 | ||||||
| chr7:152765298
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.44+5372A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152765298 | ||||||
| chr7:152765360
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.44+5434G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152765360 | ||||||
| chr7:152765415
|
C | CT | 8 | a0001c0001t0001g0137a0001c0001t0001g0181a0001c0001t0001g0182others(5): Show | 8 | HG00735.hp1 HG02135.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.44+5506dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152765415 | |||||
| chr7:152765593
|
T | A | 1 | a0001c0001t0001g0108 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.44+5667T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152765593 | ||||||
| chr7:152765970
|
A | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.44+6044A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152765970 | ||||||
| chr7:152766326
|
A | G | 122 | a0001c0001t0001g0003a0001c0001t0001g0184a0001c0001t0001g0186others(119): Show | 123 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.44+6400A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152766326 | ||||||
| chr7:152766386
|
C | T | 6 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(3): Show | 6 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.44+6460C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152766386 | ||||||
| chr7:152766477
|
G | A | 6 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(3): Show | 6 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.44+6551G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152766477 | ||||||
| chr7:152766617
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.44+6691T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152766617 | ||||||
| chr7:152766686
|
A | G | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.44+6760A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152766686 | ||||||
| chr7:152766803
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.44+6877T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152766803 | ||||||
| chr7:152766890
|
G | A | 6 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(3): Show | 6 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.44+6964G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152766890 | ||||||
| chr7:152767013
|
C | G | 5 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0242others(2): Show | 5 | HG00735.hp1 HG01891.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.44+7087C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152767013 | ||||||
| chr7:152767093
|
G | GT | 31 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(28): Show | 31 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.44+7183dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152767093 | |||||
| chr7:152767093
|
GT | G | 128 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(125): Show | 128 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.44+7183delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152767093 | |||||
| chr7:152767093
|
GTT | G | 118 | a0001c0001t0001g0003a0001c0001t0001g0184a0001c0001t0001g0186others(115): Show | 119 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.44+7182_44+7183del others(2): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152767093 | |||||
| chr7:152767235
|
C | G | 1 | a0001c0001t0002g0097 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.44+7309C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152767235 | ||||||
| chr7:152767306
|
A | G | 73 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(70): Show | 73 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.44+7380A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152767306 | ||||||
| chr7:152767348
|
A | G | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.44+7422A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152767348 | ||||||
| chr7:152767390
|
G | T | 1 | a0001c0001t0001g0234 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.44+7464G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152767390 | ||||||
| chr7:152767434
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.44+7508C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152767434 | ||||||
| chr7:152767464
|
T | C | 8 | a0001c0001t0003g0166a0001c0001t0003g0168a0001c0001t0003g0173others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.44+7538T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152767464 | ||||||
| chr7:152767529
|
A | C | 9 | a0001c0001t0001g0003a0001c0001t0001g0288a0001c0001t0001g0289others(6): Show | 10 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.44+7603A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152767529 | ||||||
| chr7:152767575
|
T | C | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.44+7649T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152767575 | ||||||
| chr7:152767591
|
A | G | 4 | a0001c0001t0001g0022a0001c0001t0001g0118a0001c0001t0001g0119others(1): Show | 4 | HG01361.hp1 HG01496.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.44+7665A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152767591 | ||||||
| chr7:152767679
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.44+7753G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152767679 | ||||||
| chr7:152767835
|
A | G | 8 | a0001c0001t0001g0296a0001c0001t0002g0002a0001c0001t0002g0019others(5): Show | 9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.44+7909A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152767835 | ||||||
| chr7:152767853
|
G | A | 11 | a0001c0001t0003g0166a0001c0001t0003g0168a0001c0001t0003g0173others(8): Show | 11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.44+7927G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152767853 | ||||||
| chr7:152767875
|
T | C | 122 | a0001c0001t0001g0003a0001c0001t0001g0184a0001c0001t0001g0186others(119): Show | 123 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.44+7949T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152767875 | ||||||
| chr7:152767980
|
C | T | 5 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0242others(2): Show | 5 | HG00735.hp1 HG01891.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.44+8054C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152767980 | ||||||
| chr7:152768173
|
A | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.44+8247A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152768173 | ||||||
| chr7:152768203
|
A | G | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0242others(1): Show | 4 | HG00735.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.44+8277A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152768203 | ||||||
| chr7:152768241
|
C | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.44+8315C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152768241 | ||||||
| chr7:152768419
|
T | C | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.44+8493T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152768419 | ||||||
| chr7:152768468
|
C | T | 8 | a0001c0001t0001g0296a0001c0001t0002g0002a0001c0001t0002g0019others(5): Show | 9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.44+8542C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152768468 | ||||||
| chr7:152768633
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.44+8707C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152768633 | ||||||
| chr7:152768664
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.44+8738C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152768664 | ||||||
| chr7:152768696
|
G | A | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.44+8770G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152768696 | ||||||
| chr7:152768733
|
C | T | 1 | a0001c0001t0001g0302 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.44+8807C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152768733 | ||||||
| chr7:152768766
|
G | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.44+8840G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152768766 | ||||||
| chr7:152768766
|
G | T | 18 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.44+8840G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152768766 | ||||||
| chr7:152768775
|
T | G | 10 | a0001c0001t0002g0007a0001c0001t0002g0155a0001c0001t0002g0156others(7): Show | 10 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.44+8849T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152768775 | ||||||
| chr7:152768787
|
T | C | 6 | a0001c0001t0001g0022a0001c0001t0001g0108a0001c0001t0001g0118others(3): Show | 6 | HG01081.hp2 HG01192.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.44+8861T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152768787 | ||||||
| chr7:152768889
|
T | G | 1 | a0001c0001t0001g0147 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.44+8963T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152768889 | ||||||
| chr7:152768893
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.44+8967G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152768893 | ||||||
| chr7:152769000
|
C | T | 1 | a0001c0001t0001g0302 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.44+9074C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152769000 | ||||||
| chr7:152769066
|
T | G | 1 | a0001c0001t0002g0101 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.44+9140T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152769066 | ||||||
| chr7:152769161
|
T | TTG | 11 | a0001c0001t0003g0166a0001c0001t0003g0168a0001c0001t0003g0173others(8): Show | 11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.44+9247_44+9248dup others(2): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152769161 | |||||
| chr7:152769207
|
T | A | 1 | a0001c0001t0002g0071 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.44+9281T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152769207 | ||||||
| chr7:152769213
|
C | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.44+9287C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152769213 | ||||||
| chr7:152769289
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.44+9363A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152769289 | ||||||
| chr7:152769298
|
C | A | 1 | a0001c0001t0001g0148 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.44+9372C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152769298 | ||||||
| chr7:152769431
|
T | G | 1 | a0001c0001t0001g0293 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.44+9505T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152769431 | ||||||
| chr7:152769574
|
G | A | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.44+9648G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152769574 | ||||||
| chr7:152769782
|
T | C | 25 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0009others(22): Show | 25 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.44+9856T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152769782 | ||||||
| chr7:152769869
|
T | TA | 15 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0002g0007others(12): Show | 15 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.44+9958dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152769869 | |||||
| chr7:152769869
|
TA | T | 114 | a0001c0001t0001g0003a0001c0001t0001g0184a0001c0001t0001g0186others(111): Show | 115 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.44+9958delA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152769869 | |||||
| chr7:152770295
|
G | A | 19 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(16): Show | 19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.44+10369G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152770295 | ||||||
| chr7:152770357
|
T | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0201a0001c0001t0001g0202others(93): Show | 97 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.44+10431T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152770357 | ||||||
| chr7:152770445
|
C | G | 11 | a0001c0001t0003g0166a0001c0001t0003g0168a0001c0001t0003g0173others(8): Show | 11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.44+10519C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152770445 | ||||||
| chr7:152770468
|
G | A | 96 | a0001c0001t0001g0200a0001c0001t0002g0004a0001c0001t0002g0005others(93): Show | 96 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.44+10542G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152770468 | ||||||
| chr7:152770683
|
T | C | 2 | a0001c0001t0001g0110a0001c0001t0001g0159 | 2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.44+10757T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152770683 | ||||||
| chr7:152770712
|
A | G | 1 | a0001c0001t0001g0269 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.44+10786A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152770712 | ||||||
| chr7:152770720
|
T | C | 1 | a0001c0001t0002g0031 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.44+10794T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152770720 | ||||||
| chr7:152770726
|
AC | A | 8 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(5): Show | 8 | HG02486.hp1 HG02717.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.44+10802delC | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152770726 | |||||
| chr7:152770784
|
A | G | 115 | a0001c0001t0001g0003a0001c0001t0001g0184a0001c0001t0001g0186others(112): Show | 116 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.44+10858A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152770784 | ||||||
| chr7:152770786
|
C | A | 115 | a0001c0001t0001g0003a0001c0001t0001g0184a0001c0001t0001g0186others(112): Show | 116 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.44+10860C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152770786 | ||||||
| chr7:152770807
|
G | A | 115 | a0001c0001t0001g0003a0001c0001t0001g0184a0001c0001t0001g0186others(112): Show | 116 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.44+10881G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152770807 | ||||||
| chr7:152770872
|
T | C | 115 | a0001c0001t0001g0003a0001c0001t0001g0184a0001c0001t0001g0186others(112): Show | 116 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.44+10946T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152770872 | ||||||
| chr7:152770995
|
G | A | 115 | a0001c0001t0001g0003a0001c0001t0001g0184a0001c0001t0001g0186others(112): Show | 116 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.44+11069G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152770995 | ||||||
| chr7:152771062
|
T | C | 115 | a0001c0001t0001g0003a0001c0001t0001g0184a0001c0001t0001g0186others(112): Show | 116 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.44+11136T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152771062 | ||||||
| chr7:152771062
|
T | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.44+11136T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152771062 | ||||||
| chr7:152771131
|
T | G | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.44+11205T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152771131 | ||||||
| chr7:152771297
|
A | G | 115 | a0001c0001t0001g0003a0001c0001t0001g0184a0001c0001t0001g0186others(112): Show | 116 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.44+11371A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152771297 | ||||||
| chr7:152771373
|
A | C | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.44+11447A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152771373 | ||||||
| chr7:152771428
|
T | G | 8 | a0001c0001t0003g0166a0001c0001t0003g0168a0001c0001t0003g0173others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.44+11502T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152771428 | ||||||
| chr7:152771507
|
C | T | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.44+11581C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152771507 | ||||||
| chr7:152771541
|
G | A | 1 | a0001c0001t0002g0007 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.44+11615G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152771541 | ||||||
| chr7:152771636
|
T | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.45-11551T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152771636 | ||||||
| chr7:152771655
|
A | C | 1 | a0001c0001t0001g0263 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.45-11532A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152771655 | ||||||
| chr7:152771761
|
G | A | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.45-11426G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152771761 | ||||||
| chr7:152771804
|
G | A | 6 | a0001c0001t0001g0242a0001c0001t0001g0266a0001c0001t0002g0026others(3): Show | 6 | HG02280.hp1 HG02451.hp1 NA19030.hp1 others(3): Show |
intron_variant | MODIFIER | c.45-11383G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152771804 | ||||||
| chr7:152771851
|
A | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.45-11336A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152771851 | ||||||
| chr7:152771863
|
G | A | 6 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0009others(3): Show | 6 | NA18949.hp2 NA18951.hp2 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.45-11324G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152771863 | ||||||
| chr7:152771919
|
G | A | 1 | a0001c0001t0002g0080 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.45-11268G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152771919 | ||||||
| chr7:152772133
|
C | A | 122 | a0001c0001t0001g0003a0001c0001t0001g0184a0001c0001t0001g0186others(119): Show | 123 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.45-11054C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152772133 | ||||||
| chr7:152772146
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.45-11041A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152772146 | ||||||
| chr7:152772307
|
C | T | 1 | a0001c0001t0002g0097 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.45-10880C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152772307 | ||||||
| chr7:152772313
|
G | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0201a0001c0001t0001g0202others(93): Show | 97 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.45-10874G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152772313 | ||||||
| chr7:152772321
|
A | C | 122 | a0001c0001t0001g0003a0001c0001t0001g0184a0001c0001t0001g0186others(119): Show | 123 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.45-10866A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152772321 | ||||||
| chr7:152772333
|
ACATAG | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.45-10851_45-10847d others(7): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152772333 | |||||
| chr7:152772351
|
T | A | 1 | a0001c0001t0001g0269 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.45-10836T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152772351 | ||||||
| chr7:152772396
|
G | A | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.45-10791G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152772396 | ||||||
| chr7:152772437
|
A | T | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.45-10750A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152772437 | ||||||
| chr7:152772456
|
T | TCAAGGTT others(4): Show |
1 | a0001c0001t0002g0010 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.45-10730_45-10720d others(13): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152772456 | |||||
| chr7:152772526
|
A | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.45-10661A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152772526 | ||||||
| chr7:152772532
|
A | G | 10 | a0001c0001t0001g0003a0001c0001t0001g0269a0001c0001t0001g0288others(7): Show | 11 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.45-10655A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152772532 | ||||||
| chr7:152772636
|
C | T | 1 | a0001c0001t0002g0031 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.45-10551C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152772636 | ||||||
| chr7:152772695
|
C | T | 2 | a0001c0001t0001g0238a0001c0001t0001g0268 | 2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.45-10492C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152772695 | ||||||
| chr7:152772733
|
A | G | 306 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(303): Show | 309 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(306): Show |
intron_variant | MODIFIER | c.45-10454A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152772733 | ||||||
| chr7:152772770
|
A | G | 6 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(3): Show | 6 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.45-10417A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152772770 | ||||||
| chr7:152772963
|
ATATG | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0201a0001c0001t0001g0202others(93): Show | 97 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.45-10221_45-10218d others(6): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152772963 | |||||
| chr7:152772988
|
A | AT | 94 | a0001c0001t0001g0200a0001c0001t0002g0004a0001c0001t0002g0005others(91): Show | 94 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.45-10192dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152772988 | |||||
| chr7:152773144
|
A | G | 1 | a0001c0001t0004g0170 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.45-10043A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152773144 | ||||||
| chr7:152773152
|
CAA | C | 115 | a0001c0001t0001g0003a0001c0001t0001g0184a0001c0001t0001g0186others(112): Show | 116 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.45-10034_45-10033d others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152773152 | ||||||
| chr7:152773314
|
G | A | 8 | a0001c0001t0001g0296a0001c0001t0002g0002a0001c0001t0002g0019others(5): Show | 9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.45-9873G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152773314 | ||||||
| chr7:152773403
|
A | G | 1 | a0001c0001t0002g0058 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.45-9784A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152773403 | ||||||
| chr7:152773485
|
G | A | 9 | a0001c0001t0001g0003a0001c0001t0001g0288a0001c0001t0001g0289others(6): Show | 10 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.45-9702G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152773485 | ||||||
| chr7:152774045
|
C | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0159 | 2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.45-9142C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774045 | ||||||
| chr7:152774174
|
T | A | 18 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.45-9013T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774174 | ||||||
| chr7:152774203
|
C | T | 96 | a0001c0001t0001g0200a0001c0001t0002g0004a0001c0001t0002g0005others(93): Show | 96 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.45-8984C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774203 | ||||||
| chr7:152774223
|
G | A | 8 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0064others(5): Show | 8 | HG01257.hp2 NA18939.hp1 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.45-8964G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774223 | ||||||
| chr7:152774244
|
C | T | 19 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(16): Show | 19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.45-8943C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774244 | ||||||
| chr7:152774285
|
C | T | 1 | a0001c0001t0002g0006 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.45-8902C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774285 | ||||||
| chr7:152774292
|
G | A | 23 | a0001c0001t0001g0120a0001c0001t0001g0122a0001c0001t0001g0123others(20): Show | 23 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.45-8895G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774292 | ||||||
| chr7:152774315
|
T | C | 2 | a0001c0001t0002g0064a0001c0001t0002g0081 | 2 | NA18950.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.45-8872T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774315 | ||||||
| chr7:152774382
|
T | A | 4 | a0001c0001t0001g0203a0001c0001t0001g0245a0001c0001t0001g0246others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.45-8805T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774382 | ||||||
| chr7:152774405
|
G | T | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.45-8782G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774405 | ||||||
| chr7:152774439
|
AT | A | 97 | a0001c0001t0001g0003a0001c0001t0001g0201a0001c0001t0001g0202others(94): Show | 98 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.45-8736delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152774439 | |||||
| chr7:152774716
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.45-8471A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774716 | ||||||
| chr7:152774721
|
A | T | 9 | a0001c0001t0001g0003a0001c0001t0001g0288a0001c0001t0001g0289others(6): Show | 10 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.45-8466A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774721 | ||||||
| chr7:152774752
|
C | G | 1 | a0001c0001t0001g0305 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.45-8435C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774752 | ||||||
| chr7:152774775
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.45-8412C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774775 | ||||||
| chr7:152774849
|
A | G | 18 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.45-8338A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774849 | ||||||
| chr7:152774862
|
G | T | 11 | a0001c0001t0003g0166a0001c0001t0003g0168a0001c0001t0003g0173others(8): Show | 11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.45-8325G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774862 | ||||||
| chr7:152774863
|
C | T | 11 | a0001c0001t0003g0166a0001c0001t0003g0168a0001c0001t0003g0173others(8): Show | 11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.45-8324C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774863 | ||||||
| chr7:152774946
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.45-8241G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774946 | ||||||
| chr7:152774960
|
A | C | 129 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(126): Show | 130 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.45-8227A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774960 | ||||||
| chr7:152775060
|
C | T | 6 | a0001c0001t0001g0296a0001c0001t0001g0299a0001c0001t0001g0304others(3): Show | 7 | HG01884.hp2 HG01952.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.45-8127C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152775060 | ||||||
| chr7:152775190
|
C | CA | 35 | a0001c0001t0001g0003a0001c0001t0001g0112a0001c0001t0001g0113others(32): Show | 36 | HG00642.hp2 HG01099.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.45-7971dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152775190 | |||||
| chr7:152775190
|
C | CAA | 11 | a0001c0001t0001g0111a0001c0001t0001g0205a0001c0001t0001g0206others(8): Show | 11 | HG01496.hp1 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.45-7972_45-7971dup others(2): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152775190 | |||||
| chr7:152775190
|
CA | C | 77 | a0001c0001t0001g0015a0001c0001t0001g0200a0001c0001t0001g0232others(74): Show | 77 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.45-7971delA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152775190 | |||||
| chr7:152775190
|
CAA | C | 10 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0299others(7): Show | 10 | HG01070.hp2 HG01952.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.45-7972_45-7971del others(2): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152775190 | |||||
| chr7:152775215
|
AAG | A | 7 | a0001c0001t0003g0166a0001c0001t0003g0168a0001c0001t0003g0173others(4): Show | 7 | HG02280.hp2 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.45-7970_45-7969del others(2): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152775215 | |||||
| chr7:152775216
|
AG | A | 3 | a0001c0001t0003g0286a0001c0001t0004g0169a0001c0001t0004g0170 | 3 | HG02976.hp2 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.45-7970delG | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152775216 | ||||||
| chr7:152775217
|
G | A | 1 | a0001c0001t0004g0176 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.45-7970G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152775217 | ||||||
| chr7:152775448
|
C | T | 2 | a0001c0001t0002g0077a0001c0001t0002g0078 | 2 | HG02074.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.45-7739C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152775448 | ||||||
| chr7:152775743
|
G | A | 115 | a0001c0001t0001g0003a0001c0001t0001g0184a0001c0001t0001g0186others(112): Show | 116 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.45-7444G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152775743 | ||||||
| chr7:152775759
|
C | CA | 27 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0184others(24): Show | 27 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.45-7414dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152775759 | |||||
| chr7:152775774
|
T | C | 5 | a0001c0001t0001g0203a0001c0001t0001g0208a0001c0001t0001g0245others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.45-7413T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152775774 | ||||||
| chr7:152775839
|
A | G | 6 | a0001c0001t0001g0022a0001c0001t0001g0108a0001c0001t0001g0118others(3): Show | 6 | HG01081.hp2 HG01192.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.45-7348A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152775839 | ||||||
| chr7:152775841
|
G | A | 2 | a0001c0001t0002g0156a0001c0001t0002g0165 | 2 | HG01074.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.45-7346G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152775841 | ||||||
| chr7:152776137
|
A | G | 2 | a0001c0001t0003g0174a0001c0001t0003g0175 | 2 | HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.45-7050A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152776137 | ||||||
| chr7:152776219
|
T | C | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.45-6968T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152776219 | ||||||
| chr7:152776247
|
G | C | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.45-6940G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152776247 | ||||||
| chr7:152776532
|
C | G | 2 | a0001c0001t0001g0265a0001c0001t0001g0302 | 2 | HG01891.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.45-6655C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152776532 | ||||||
| chr7:152776576
|
A | C | 2 | a0001c0001t0001g0238a0001c0001t0001g0268 | 2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.45-6611A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152776576 | ||||||
| chr7:152776677
|
A | G | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.45-6510A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152776677 | ||||||
| chr7:152776882
|
A | G | 1 | a0001c0001t0001g0302 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.45-6305A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152776882 | ||||||
| chr7:152776954
|
A | G | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.45-6233A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152776954 | ||||||
| chr7:152776956
|
A | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.45-6231A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152776956 | ||||||
| chr7:152776969
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.45-6218C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152776969 | ||||||
| chr7:152776970
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.45-6217G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152776970 | ||||||
| chr7:152777015
|
C | T | 1 | a0001c0001t0002g0096 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.45-6172C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152777015 | ||||||
| chr7:152777016
|
G | A | 8 | a0001c0001t0001g0296a0001c0001t0002g0002a0001c0001t0002g0019others(5): Show | 9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.45-6171G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152777016 | ||||||
| chr7:152777026
|
G | T | 1 | a0001c0001t0001g0260 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.45-6161G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152777026 | ||||||
| chr7:152777388
|
T | C | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.45-5799T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152777388 | ||||||
| chr7:152777438
|
C | T | 1 | a0002c0006t0001g0189 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.45-5749C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152777438 | ||||||
| chr7:152777525
|
GTTC | G | 6 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(3): Show | 6 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.45-5659_45-5657del others(3): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152777525 | |||||
| chr7:152777564
|
A | G | 1 | a0001c0001t0002g0007 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.45-5623A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152777564 | ||||||
| chr7:152777624
|
C | T | 119 | a0001c0001t0001g0003a0001c0001t0001g0184a0001c0001t0001g0186others(116): Show | 120 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.45-5563C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152777624 | ||||||
| chr7:152777644
|
T | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.45-5543T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152777644 | ||||||
| chr7:152777750
|
A | C | 1 | a0001c0001t0001g0132 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.45-5437A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152777750 | ||||||
| chr7:152777865
|
G | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.45-5322G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152777865 | ||||||
| chr7:152777940
|
A | AC | 11 | a0001c0001t0003g0166a0001c0001t0003g0168a0001c0001t0003g0173others(8): Show | 11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.45-5246dupC | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152777940 | |||||
| chr7:152778156
|
T | C | 298 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(295): Show | 301 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(298): Show |
intron_variant | MODIFIER | c.45-5031T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152778156 | ||||||
| chr7:152778227
|
A | AT | 12 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(9): Show | 12 | HG00735.hp2 HG01099.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.45-4943dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778227 | |||||
| chr7:152778227
|
AT | A | 19 | a0001c0001t0001g0152a0001c0001t0001g0184a0001c0001t0001g0186others(16): Show | 19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.45-4943delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778227 | |||||
| chr7:152778227
|
ATT | A | 101 | a0001c0001t0001g0003a0001c0001t0001g0201a0001c0001t0001g0202others(98): Show | 102 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.45-4944_45-4943del others(2): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778227 | |||||
| chr7:152778261
|
T | A | 19 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(16): Show | 19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.45-4926T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152778261 | ||||||
| chr7:152778377
|
G | A | 235 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(232): Show | 236 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.45-4810G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152778377 | ||||||
| chr7:152778443
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.45-4744G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152778443 | ||||||
| chr7:152778668
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.45-4519G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152778668 | ||||||
| chr7:152778791
|
A | T | 10 | a0001c0001t0002g0007a0001c0001t0002g0155a0001c0001t0002g0156others(7): Show | 10 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.45-4396A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152778791 | ||||||
| chr7:152778891
|
C | T | 18 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.45-4296C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152778891 | ||||||
| chr7:152778911
|
C | G | 1 | a0001c0001t0002g0006 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.45-4276C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152778911 | ||||||
| chr7:152778943
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0148 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.45-4211_45-4202dup others(10): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | |||||
| chr7:152778943
|
C | CAAAAAAA others(4): Show |
2 | a0001c0001t0002g0007a0001c0001t0002g0155 | 2 | HG02896.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.45-4212_45-4202dup others(11): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | |||||
| chr7:152778943
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0122 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.45-4218_45-4202dup others(17): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | |||||
| chr7:152778943
|
CA | C | 9 | a0001c0001t0001g0022a0001c0001t0001g0108a0001c0001t0001g0120others(6): Show | 9 | HG01081.hp2 HG02809.hp1 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.45-4202delA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | |||||
| chr7:152778943
|
CAA | C | 8 | a0001c0001t0001g0112a0001c0001t0001g0121a0001c0001t0001g0123others(5): Show | 8 | HG00597.hp1 HG01496.hp1 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.45-4203_45-4202del others(2): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | |||||
| chr7:152778943
|
CAAA | C | 13 | a0001c0001t0001g0113a0001c0001t0001g0129a0001c0001t0001g0130others(10): Show | 13 | HG00544.hp2 HG01074.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.45-4204_45-4202del others(3): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | |||||
| chr7:152778943
|
CAAAA | C | 11 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0115others(8): Show | 12 | HG01099.hp1 HG01255.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.45-4205_45-4202del others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | |||||
| chr7:152778943
|
CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0002g0021a0001c0001t0002g0028a0001c0001t0002g0086 | 3 | HG01346.hp1 HG02132.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.45-4212_45-4202del others(11): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | |||||
| chr7:152778943
|
CAAAAAAA others(5): Show |
C | 34 | a0001c0001t0001g0182a0001c0001t0002g0010a0001c0001t0002g0017others(31): Show | 34 | HG00438.hp1 HG00735.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.45-4213_45-4202del others(12): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | |||||
| chr7:152778943
|
CAAAAAAA others(6): Show |
C | 51 | a0001c0001t0001g0200a0001c0001t0002g0004a0001c0001t0002g0005others(48): Show | 51 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.45-4214_45-4202del others(13): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | |||||
| chr7:152778943
|
CAAAAAAA others(7): Show |
C | 7 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0107others(4): Show | 7 | HG01361.hp2 HG02486.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.45-4215_45-4202del others(14): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | |||||
| chr7:152778943
|
CAAAAAAA others(8): Show |
C | 11 | a0001c0001t0001g0296a0001c0001t0002g0002a0001c0001t0002g0179others(8): Show | 12 | HG01884.hp2 HG01891.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.45-4216_45-4202del others(15): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | |||||
| chr7:152778943
|
CAAAAAAA others(9): Show |
C | 22 | a0001c0001t0001g0110a0001c0001t0001g0205a0001c0001t0001g0206others(19): Show | 22 | HG00099.hp1 HG00423.hp2 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.45-4217_45-4202del others(16): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | |||||
| chr7:152778943
|
CAAAAAAA others(10): Show |
C | 68 | a0001c0001t0001g0003a0001c0001t0001g0184a0001c0001t0001g0190others(65): Show | 69 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.45-4218_45-4202del others(17): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | |||||
| chr7:152778943
|
CAAAAAAA others(11): Show |
C | 26 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(23): Show | 26 | HG01109.hp1 HG01256.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.45-4219_45-4202del others(18): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | |||||
| chr7:152778943
|
CAAAAAAA others(12): Show |
C | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0269others(1): Show | 4 | HG00735.hp1 HG02723.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.45-4220_45-4202del others(19): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | |||||
| chr7:152778943
|
CAAAAAAA others(15): Show |
C | 4 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(1): Show | 4 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.45-4223_45-4202del others(22): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | |||||
| chr7:152778943
|
CAAAAAAA others(16): Show |
C | 1 | a0001c0001t0001g0119 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.45-4224_45-4202del others(23): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | |||||
| chr7:152778943
|
CAAAAAAA others(19): Show |
C | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(3): Show | 6 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.45-4227_45-4202del others(26): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | |||||
| chr7:152778943
|
CAAAAAAA others(23): Show |
C | 7 | a0001c0001t0002g0051a0001c0001t0002g0052a0001c0001t0002g0053others(4): Show | 7 | NA18942.hp2 NA18971.hp1 NA18990.hp2 others(4): Show |
intron_variant | MODIFIER | c.45-4231_45-4202del others(30): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | |||||
| chr7:152778985
|
A | G | 1 | a0001c0001t0002g0032 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.45-4202A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152778985 | ||||||
| chr7:152779014
|
C | G | 81 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(78): Show | 81 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.45-4173C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152779014 | ||||||
| chr7:152779038
|
T | G | 115 | a0001c0001t0001g0003a0001c0001t0001g0184a0001c0001t0001g0186others(112): Show | 116 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.45-4149T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152779038 | ||||||
| chr7:152779044
|
C | T | 122 | a0001c0001t0001g0003a0001c0001t0001g0184a0001c0001t0001g0186others(119): Show | 123 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.45-4143C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152779044 | ||||||
| chr7:152779203
|
G | C | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.45-3984G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152779203 | ||||||
| chr7:152779257
|
C | T | 8 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0298others(5): Show | 8 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.45-3930C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152779257 | ||||||
| chr7:152779259
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.45-3928C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152779259 | ||||||
| chr7:152779263
|
C | T | 8 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0298others(5): Show | 8 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.45-3924C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152779263 | ||||||
| chr7:152779264
|
A | G | 9 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0298others(6): Show | 9 | HG01952.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.45-3923A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152779264 | ||||||
| chr7:152779456
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.45-3731C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152779456 | ||||||
| chr7:152779496
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.45-3691C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152779496 | ||||||
| chr7:152779700
|
A | C | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.45-3487A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152779700 | ||||||
| chr7:152779732
|
G | C | 1 | a0001c0001t0005g0183 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.45-3455G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152779732 | ||||||
| chr7:152779996
|
T | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.45-3191T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152779996 | ||||||
| chr7:152780011
|
C | T | 1 | a0001c0001t0002g0054 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.45-3176C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780011 | ||||||
| chr7:152780118
|
T | C | 4 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0177others(1): Show | 4 | HG01361.hp2 HG01934.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.45-3069T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780118 | ||||||
| chr7:152780158
|
T | C | 4 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0177others(1): Show | 4 | HG01361.hp2 HG01934.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.45-3029T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780158 | ||||||
| chr7:152780166
|
C | T | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0242others(1): Show | 4 | HG00735.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.45-3021C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780166 | ||||||
| chr7:152780190
|
C | A | 2 | a0001c0001t0001g0119a0001c0001t0002g0067 | 2 | HG01361.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.45-2997C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780190 | ||||||
| chr7:152780208
|
G | A | 1 | a0001c0001t0002g0067 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.45-2979G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780208 | ||||||
| chr7:152780208
|
G | C | 220 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.45-2979G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780208 | ||||||
| chr7:152780266
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.45-2921G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780266 | ||||||
| chr7:152780283
|
G | A | 222 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(220): Show |
intron_variant | MODIFIER | c.45-2904G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780283 | ||||||
| chr7:152780329
|
C | G | 229 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(226): Show | 230 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.45-2858C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780329 | ||||||
| chr7:152780339
|
C | T | 229 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(226): Show | 230 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.45-2848C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780339 | ||||||
| chr7:152780352
|
C | CAA | 217 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(214): Show | 218 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.45-2822_45-2821dup others(2): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152780352 | |||||
| chr7:152780395
|
G | A | 220 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.45-2792G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780395 | ||||||
| chr7:152780456
|
C | G | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.45-2731C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780456 | ||||||
| chr7:152780487
|
A | T | 235 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(232): Show | 236 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.45-2700A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780487 | ||||||
| chr7:152780530
|
T | C | 7 | a0001c0001t0001g0188a0001c0001t0001g0302a0001c0001t0002g0026others(4): Show | 7 | HG02280.hp1 HG02630.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.45-2657T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780530 | ||||||
| chr7:152780539
|
G | A | 2 | a0001c0001t0001g0188a0001c0001t0008g0307 | 2 | HG02965.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.45-2648G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780539 | ||||||
| chr7:152780569
|
T | C | 1 | a0001c0001t0008g0307 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.45-2618T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780569 | ||||||
| chr7:152780844
|
A | AT | 9 | a0001c0001t0001g0124a0001c0001t0001g0132a0001c0001t0002g0044others(6): Show | 9 | HG00438.hp2 HG00735.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.45-2325dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152780844 | |||||
| chr7:152780844
|
A | ATT | 10 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0302others(7): Show | 10 | HG01952.hp1 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.45-2326_45-2325dup others(2): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152780844 | |||||
| chr7:152780844
|
AT | A | 27 | a0001c0001t0001g0147a0001c0001t0001g0184a0001c0001t0001g0186others(24): Show | 28 | HG01109.hp1 HG01192.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.45-2325delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152780844 | |||||
| chr7:152780844
|
ATT | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0201a0001c0001t0001g0202others(93): Show | 97 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.45-2326_45-2325del others(2): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152780844 | |||||
| chr7:152780888
|
C | T | 1 | a0001c0001t0002g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.45-2299C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780888 | ||||||
| chr7:152780914
|
T | C | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.45-2273T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780914 | ||||||
| chr7:152780948
|
G | C | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.45-2239G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780948 | ||||||
| chr7:152781100
|
G | T | 134 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(131): Show | 135 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.45-2087G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152781100 | ||||||
| chr7:152781143
|
T | C | 1 | a0001c0001t0001g0269 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.45-2044T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152781143 | ||||||
| chr7:152781169
|
C | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.45-2018C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152781169 | ||||||
| chr7:152781178
|
A | G | 1 | a0001c0001t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.45-2009A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152781178 | ||||||
| chr7:152781193
|
G | GT | 102 | a0001c0001t0001g0111a0001c0001t0001g0122a0001c0001t0001g0125others(99): Show | 102 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.45-1971dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152781193 | |||||
| chr7:152781193
|
G | GTT | 17 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(14): Show | 17 | HG00423.hp2 HG01099.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.45-1972_45-1971dup others(2): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152781193 | |||||
| chr7:152781193
|
GT | G | 9 | a0001c0001t0001g0108a0001c0001t0001g0298a0001c0001t0001g0299others(6): Show | 9 | HG01070.hp2 HG01081.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.45-1971delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152781193 | |||||
| chr7:152781198
|
T | G | 1 | a0001c0001t0002g0051 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.45-1989T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152781198 | ||||||
| chr7:152781299
|
T | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0201a0001c0001t0001g0202others(93): Show | 97 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.45-1888T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152781299 | ||||||
| chr7:152781356
|
G | A | 5 | a0001c0001t0002g0007a0001c0001t0002g0155a0001c0001t0002g0156others(2): Show | 5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.45-1831G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152781356 | ||||||
| chr7:152781369
|
C | T | 1 | a0001c0001t0002g0062 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.45-1818C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152781369 | ||||||
| chr7:152781375
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.45-1812T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152781375 | ||||||
| chr7:152781477
|
G | A | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.45-1710G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152781477 | ||||||
| chr7:152781767
|
C | A | 8 | a0001c0001t0001g0296a0001c0001t0002g0002a0001c0001t0002g0019others(5): Show | 9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.45-1420C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152781767 | ||||||
| chr7:152781818
|
C | T | 1 | a0001c0001t0002g0155 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.45-1369C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152781818 | ||||||
| chr7:152781911
|
C | T | 18 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.45-1276C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152781911 | ||||||
| chr7:152782033
|
G | GT | 12 | a0001c0001t0001g0003a0001c0001t0001g0269a0001c0001t0001g0288others(9): Show | 13 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.45-1145dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152782033 | |||||
| chr7:152782118
|
ATCGTAAA others(10): Show |
A | 1 | a0001c0001t0001g0215 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.45-1067_45-1051del others(17): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152782118 | |||||
| chr7:152782231
|
G | A | 134 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(131): Show | 135 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.45-956G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152782231 | ||||||
| chr7:152782289
|
G | A | 115 | a0001c0001t0001g0003a0001c0001t0001g0184a0001c0001t0001g0186others(112): Show | 116 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.45-898G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152782289 | ||||||
| chr7:152782705
|
T | C | 18 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.45-482T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152782705 | ||||||
| chr7:152782856
|
C | G | 1 | a0001c0001t0001g0187 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.45-331C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152782856 | ||||||
| chr7:152783015
|
A | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.45-172A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152783015 | ||||||
| chr7:152783043
|
G | GT | 95 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0113others(92): Show | 96 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.45-125dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152783043 | |||||
| chr7:152783043
|
G | GTT | 12 | a0001c0001t0001g0214a0001c0001t0002g0021a0001c0001t0002g0044others(9): Show | 12 | HG00438.hp1 HG01255.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.45-126_45-125dupTT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152783043 | |||||
| chr7:152783043
|
GT | G | 93 | a0001c0001t0001g0003a0001c0001t0001g0123a0001c0001t0001g0129others(90): Show | 94 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.45-125delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152783043 | |||||
| chr7:152783043
|
GTT | G | 13 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(10): Show | 13 | HG01099.hp2 HG01106.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.45-126_45-125delTT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152783043 | |||||
| chr7:152783045
|
T | G | 4 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0304others(1): Show | 4 | HG01952.hp1 HG02622.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.45-142T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152783045 | ||||||
| chr7:152783046
|
T | G | 6 | a0001c0001t0001g0302a0001c0001t0002g0157a0001c0001t0002g0158others(3): Show | 6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.45-141T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152783046 | ||||||
| chr7:152783049
|
T | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.45-138T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152783049 | ||||||
| chr7:152783141
|
G | A | 3 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0176 | 3 | HG01891.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.45-46G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152783141 | ||||||
| chr7:152783361
|
G | A | 5 | a0001c0001t0002g0007a0001c0001t0002g0155a0001c0001t0002g0156others(2): Show | 5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+119G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152783361 | ||||||
| chr7:152783426
|
G | A | 1 | a0001c0001t0008g0307 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.100+184G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152783426 | ||||||
| chr7:152783465
|
T | TGGGTCCC others(10): Show |
1 | a0001c0001t0001g0215 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.100+223_100+224ins others(17): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152783465 | ||||||
| chr7:152783479
|
C | A | 1 | a0001c0001t0001g0215 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.100+237C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152783479 | ||||||
| chr7:152783489
|
C | T | 1 | a0001c0001t0001g0215 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.100+247C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152783489 | ||||||
| chr7:152783603
|
C | T | 39 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(36): Show | 39 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.100+361C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152783603 | ||||||
| chr7:152783612
|
CT | C | 9 | a0001c0001t0001g0302a0001c0001t0002g0057a0001c0001t0002g0091others(6): Show | 9 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+381delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152783612 | |||||
| chr7:152783733
|
G | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+491G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152783733 | ||||||
| chr7:152783775
|
G | A | 74 | a0001c0001t0001g0003a0001c0001t0001g0201a0001c0001t0001g0202others(71): Show | 75 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.100+533G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152783775 | ||||||
| chr7:152783888
|
G | A | 1 | a0001c0001t0002g0088 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.100+646G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152783888 | ||||||
| chr7:152783926
|
T | C | 1 | a0001c0003t0003g0167 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.100+684T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152783926 | ||||||
| chr7:152783957
|
G | A | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.100+715G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152783957 | ||||||
| chr7:152783958
|
C | G | 6 | a0001c0001t0001g0302a0001c0001t0002g0157a0001c0001t0002g0158others(3): Show | 6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+716C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152783958 | ||||||
| chr7:152784017
|
G | A | 23 | a0001c0001t0001g0120a0001c0001t0001g0122a0001c0001t0001g0123others(20): Show | 23 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.100+775G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152784017 | ||||||
| chr7:152784045
|
G | A | 18 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.100+803G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152784045 | ||||||
| chr7:152784090
|
CA | C | 6 | a0001c0001t0001g0152a0001c0001t0001g0212a0001c0001t0002g0009others(3): Show | 6 | HG01257.hp2 HG02965.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.100+861delA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152784090 | |||||
| chr7:152784281
|
G | A | 1 | a0001c0001t0002g0178 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.100+1039G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152784281 | ||||||
| chr7:152784298
|
G | A | 2 | a0001c0001t0001g0299a0001c0001t0001g0304 | 2 | HG01952.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.100+1056G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152784298 | ||||||
| chr7:152784303
|
G | A | 2 | a0001c0001t0001g0207a0001c0001t0001g0247 | 2 | HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.100+1061G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152784303 | ||||||
| chr7:152784491
|
T | G | 1 | a0001c0001t0001g0161 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.100+1249T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152784491 | ||||||
| chr7:152784577
|
T | C | 1 | a0001c0001t0002g0028 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.100+1335T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152784577 | ||||||
| chr7:152784657
|
C | G | 1 | a0001c0001t0002g0028 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.100+1415C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152784657 | ||||||
| chr7:152784694
|
G | C | 1 | a0001c0001t0002g0028 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.100+1452G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152784694 | ||||||
| chr7:152784707
|
T | C | 1 | a0001c0001t0002g0028 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.100+1465T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152784707 | ||||||
| chr7:152784774
|
G | A | 74 | a0001c0001t0001g0003a0001c0001t0001g0201a0001c0001t0001g0202others(71): Show | 75 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.100+1532G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152784774 | ||||||
| chr7:152784844
|
C | T | 6 | a0001c0001t0001g0302a0001c0001t0002g0157a0001c0001t0002g0158others(3): Show | 6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+1602C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152784844 | ||||||
| chr7:152784867
|
C | T | 18 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.100+1625C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152784867 | ||||||
| chr7:152784948
|
C | T | 20 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0225others(17): Show | 20 | HG00738.hp1 HG01071.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.100+1706C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152784948 | ||||||
| chr7:152785017
|
C | T | 8 | a0001c0001t0001g0296a0001c0001t0002g0002a0001c0001t0002g0019others(5): Show | 9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+1775C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785017 | ||||||
| chr7:152785026
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.100+1784C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785026 | ||||||
| chr7:152785086
|
CTTG | C | 9 | a0001c0001t0001g0003a0001c0001t0001g0288a0001c0001t0001g0289others(6): Show | 10 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.100+1847_100+1849d others(5): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785086 | |||||
| chr7:152785146
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.100+1904A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785146 | ||||||
| chr7:152785271
|
G | A | 37 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(34): Show | 37 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.100+2029G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785271 | ||||||
| chr7:152785374
|
TGTGAGGG others(103): Show |
T | 3 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0176 | 3 | HG01891.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.100+2134_100+2243d others(2): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785374 | |||||
| chr7:152785374
|
TGTGAGGG others(105): Show |
T | 8 | a0001c0001t0003g0166a0001c0001t0003g0168a0001c0001t0003g0173others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.100+2134_100+2245d others(2): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785374 | |||||
| chr7:152785376
|
T | TG | 39 | a0001c0001t0001g0192a0001c0001t0001g0234a0001c0001t0001g0241others(36): Show | 39 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.100+2135dupG | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785376 | |||||
| chr7:152785376
|
T | TGA | 6 | a0001c0001t0001g0200a0001c0001t0002g0060a0001c0001t0002g0066others(3): Show | 6 | HG00099.hp1 HG00738.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+2136_100+2137d others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785376 | |||||
| chr7:152785376
|
T | TGAGAGA | 10 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0298others(7): Show | 10 | HG01934.hp2 HG01952.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.100+2137_100+2138i others(8): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785376 | |||||
| chr7:152785376
|
T | TGG | 10 | a0001c0001t0001g0213a0001c0001t0001g0257a0001c0001t0002g0018others(7): Show | 10 | HG00735.hp2 HG01168.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.100+2135_100+2136i others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785376 | |||||
| chr7:152785377
|
GA | G | 14 | a0001c0001t0001g0187a0001c0001t0001g0191a0001c0001t0001g0193others(11): Show | 14 | HG00738.hp1 HG02083.hp2 HG03239.hp2 others(11): Show |
intron_variant | MODIFIER | c.100+2136delA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785377 | ||||||
| chr7:152785378
|
A | AG | 21 | a0001c0001t0001g0022a0001c0001t0001g0110a0001c0001t0001g0111others(18): Show | 21 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.100+2146dupG | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785378 | |||||
| chr7:152785378
|
A | G | 103 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0188others(100): Show | 103 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.100+2136A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785378 | ||||||
| chr7:152785379
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.100+2137G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785379 | ||||||
| chr7:152785379
|
G | GA | 12 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0026others(9): Show | 12 | HG02055.hp1 HG02280.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.100+2137_100+2138i others(3): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785379 | ||||||
| chr7:152785379
|
G | GAGAGA | 43 | a0001c0001t0001g0003a0001c0001t0001g0207a0001c0001t0001g0215others(40): Show | 45 | HG00597.hp2 HG00609.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.100+2137_100+2138i others(7): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785379 | ||||||
| chr7:152785380
|
G | A | 49 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0201others(46): Show | 49 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.100+2138G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785380 | ||||||
| chr7:152785381
|
G | A | 39 | a0001c0001t0001g0003a0001c0001t0001g0207a0001c0001t0001g0215others(36): Show | 41 | HG00597.hp2 HG00609.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.100+2139G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785381 | ||||||
| chr7:152785382
|
G | A | 42 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(39): Show | 42 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.100+2140G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785382 | ||||||
| chr7:152785383
|
G | C | 1 | a0001c0001t0002g0054 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.100+2141G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785383 | ||||||
| chr7:152785384
|
G | A | 42 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(39): Show | 42 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.100+2142G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785384 | ||||||
| chr7:152785386
|
G | A | 42 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(39): Show | 42 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.100+2144G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785386 | ||||||
| chr7:152785389
|
A | AGGGGAGG others(37): Show |
2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.100+2164_100+2207d others(46): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785389 | |||||
| chr7:152785389
|
A | G | 43 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(40): Show | 43 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.100+2147A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785389 | ||||||
| chr7:152785394
|
A | G | 1 | a0001c0005t0001g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.100+2152A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785394 | ||||||
| chr7:152785394
|
AG | A | 41 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(38): Show | 41 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.100+2157delG | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785394 | |||||
| chr7:152785395
|
G | A | 1 | a0001c0005t0001g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.100+2153G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785395 | ||||||
| chr7:152785402
|
GGGGAGAG others(3): Show |
G | 5 | a0001c0001t0001g0215a0001c0001t0001g0298a0001c0001t0001g0299others(2): Show | 5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+2178_100+2187d others(12): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785402 | |||||
| chr7:152785406
|
AGAGG | A | 42 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(39): Show | 42 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.100+2172_100+2175d others(6): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785406 | |||||
| chr7:152785412
|
A | G | 42 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(39): Show | 42 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.100+2170A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785412 | ||||||
| chr7:152785420
|
GGAGGGAG others(3): Show |
G | 1 | a0001c0001t0001g0117 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.100+2184_100+2193d others(12): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785420 | |||||
| chr7:152785428
|
A | AGAGAGGG others(14): Show |
1 | a0001c0001t0002g0101 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.100+2196_100+2216d others(23): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785428 | |||||
| chr7:152785432
|
A | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+2190A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785432 | ||||||
| chr7:152785432
|
AG | A | 18 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.100+2195delG | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785432 | |||||
| chr7:152785438
|
A | AGGGGGAG others(9): Show |
2 | a0001c0002t0001g0209a0001c0002t0001g0211 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.100+2208_100+2223d others(18): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785438 | |||||
| chr7:152785441
|
G | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+2199G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785441 | ||||||
| chr7:152785447
|
G | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0113a0001c0001t0001g0114others(1): Show | 5 | HG00741.hp1 HG01175.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+2205G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785447 | ||||||
| chr7:152785453
|
A | AG | 15 | a0001c0001t0001g0145a0001c0001t0001g0198a0001c0001t0001g0202others(12): Show | 15 | HG00609.hp1 HG01109.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.100+2217dupG | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785453 | |||||
| chr7:152785470
|
G | A | 2 | a0001c0001t0001g0269a0001c0001t0002g0007 | 2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.100+2228G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785470 | ||||||
| chr7:152785470
|
G | GGGAGAGG others(27): Show |
1 | a0001c0001t0002g0038 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.100+2229_100+2230i others(36): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785470 | |||||
| chr7:152785474
|
G | A | 3 | a0001c0001t0001g0269a0001c0001t0002g0007a0001c0001t0002g0038 | 3 | HG00544.hp1 HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.100+2232G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785474 | ||||||
| chr7:152785474
|
G | GGGGAGAG others(5): Show |
2 | a0001c0001t0002g0055a0001c0001t0008g0307 | 2 | HG00735.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.100+2233_100+2234i others(14): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785474 | |||||
| chr7:152785479
|
G | GAGAGAGA others(7): Show |
1 | a0001c0001t0001g0229 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.100+2251_100+2264d others(16): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785479 | |||||
| chr7:152785481
|
G | C | 3 | a0001c0001t0002g0038a0001c0001t0002g0055a0001c0001t0008g0307 | 3 | HG00544.hp1 HG00735.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.100+2239G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785481 | ||||||
| chr7:152785481
|
G | GAGACAGA others(5): Show |
1 | a0001c0001t0002g0027 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.100+2242_100+2243i others(14): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785481 | |||||
| chr7:152785481
|
G | GAGAGAGA others(3): Show |
118 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(115): Show | 120 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.100+2248_100+2249i others(12): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785481 | |||||
| chr7:152785481
|
G | GAGAGAGA others(5): Show |
115 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(112): Show | 115 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.100+2251_100+2262d others(14): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785481 | |||||
| chr7:152785481
|
G | GAGAGAGA others(7): Show |
2 | a0001c0001t0002g0033a0001c0001t0002g0043 | 2 | NA18949.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.100+2250_100+2251i others(16): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785481 | |||||
| chr7:152785493
|
C | G | 11 | a0001c0001t0003g0166a0001c0001t0003g0168a0001c0001t0003g0173others(8): Show | 11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.100+2251C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785493 | ||||||
| chr7:152785504
|
A | ACAGAGAG others(12): Show |
1 | a0001c0005t0001g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.100+2262_100+2263i others(21): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785504 | ||||||
| chr7:152785510
|
AG | A | 11 | a0001c0001t0003g0166a0001c0001t0003g0168a0001c0001t0003g0173others(8): Show | 11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.100+2270delG | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785510 | |||||
| chr7:152785512
|
G | A | 1 | a0001c0005t0001g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.100+2270G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785512 | ||||||
| chr7:152785512
|
G | GAGAGAGA | 36 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(33): Show | 36 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.100+2278_100+2284d others(9): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785512 | |||||
| chr7:152785518
|
GA | G | 11 | a0001c0001t0003g0166a0001c0001t0003g0168a0001c0001t0003g0173others(8): Show | 11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.100+2278delA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785518 | |||||
| chr7:152785542
|
G | A | 4 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0165others(1): Show | 4 | HG01074.hp2 HG01099.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+2300G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785542 | ||||||
| chr7:152785640
|
C | T | 69 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(66): Show | 70 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.100+2398C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785640 | ||||||
| chr7:152785659
|
T | C | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(3): Show | 6 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.100+2417T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785659 | ||||||
| chr7:152785721
|
C | T | 3 | a0001c0001t0002g0037a0001c0001t0002g0039a0001c0001t0002g0075 | 3 | HG00423.hp1 HG00558.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.100+2479C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785721 | ||||||
| chr7:152785722
|
G | A | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(9): Show | 12 | HG01099.hp2 HG02083.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.100+2480G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785722 | ||||||
| chr7:152785945
|
G | A | 3 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0280 | 3 | HG01167.hp2 HG01169.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.100+2703G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785945 | ||||||
| chr7:152786058
|
C | T | 138 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(135): Show | 139 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.100+2816C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786058 | ||||||
| chr7:152786084
|
G | C | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+2842G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786084 | ||||||
| chr7:152786173
|
G | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+2931G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786173 | ||||||
| chr7:152786281
|
G | A | 17 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(14): Show | 17 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.100+3039G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786281 | ||||||
| chr7:152786399
|
A | G | 16 | a0001c0001t0001g0200a0001c0001t0002g0023a0001c0001t0002g0024others(13): Show | 16 | HG00099.hp1 HG00738.hp2 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.100+3157A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786399 | ||||||
| chr7:152786410
|
C | T | 1 | a0001c0001t0002g0024 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.100+3168C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786410 | ||||||
| chr7:152786482
|
G | A | 18 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.100+3240G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786482 | ||||||
| chr7:152786548
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.100+3306G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786548 | ||||||
| chr7:152786549
|
T | C | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.100+3307T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786549 | ||||||
| chr7:152786552
|
C | T | 1 | a0001c0001t0002g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.100+3310C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786552 | ||||||
| chr7:152786552
|
CG | C | 5 | a0001c0001t0001g0302a0001c0001t0002g0157a0001c0001t0002g0158others(2): Show | 5 | HG02630.hp2 HG03490.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+3311delG | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786552 | ||||||
| chr7:152786553
|
G | A | 1 | a0001c0001t0002g0163 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.100+3311G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786553 | ||||||
| chr7:152786553
|
G | GA | 10 | a0001c0001t0001g0113a0001c0001t0001g0124a0001c0001t0001g0125others(7): Show | 10 | HG00438.hp2 HG01175.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.100+3326dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152786553 | |||||
| chr7:152786553
|
GA | G | 38 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(35): Show | 39 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.100+3326delA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152786553 | |||||
| chr7:152786659
|
A | C | 216 | a0001c0001t0001g0003a0001c0001t0001g0200a0001c0001t0001g0201others(213): Show | 218 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.100+3417A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786659 | ||||||
| chr7:152786772
|
A | G | 254 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.100+3530A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786772 | ||||||
| chr7:152786848
|
T | G | 1 | a0001c0001t0001g0215 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.100+3606T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786848 | ||||||
| chr7:152786955
|
G | A | 5 | a0001c0001t0001g0207a0001c0001t0001g0230a0001c0001t0001g0243others(2): Show | 5 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+3713G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786955 | ||||||
| chr7:152787226
|
T | C | 5 | a0001c0001t0002g0157a0001c0001t0002g0158a0001c0001t0002g0163others(2): Show | 5 | HG03490.hp1 HG03491.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+3984T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152787226 | ||||||
| chr7:152787303
|
A | C | 1 | a0001c0001t0001g0232 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.100+4061A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152787303 | ||||||
| chr7:152787352
|
T | G | 118 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(115): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.100+4110T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152787352 | ||||||
| chr7:152787681
|
C | G | 18 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.100+4439C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152787681 | ||||||
| chr7:152787711
|
C | T | 1 | a0001c0001t0002g0002 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.100+4469C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152787711 | ||||||
| chr7:152787777
|
A | G | 17 | a0001c0001t0001g0200a0001c0001t0002g0023a0001c0001t0002g0024others(14): Show | 17 | HG00099.hp1 HG00738.hp2 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.100+4535A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152787777 | ||||||
| chr7:152787811
|
C | T | 95 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0225others(92): Show | 95 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.100+4569C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152787811 | ||||||
| chr7:152787878
|
A | G | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.100+4636A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152787878 | ||||||
| chr7:152787887
|
T | C | 1 | a0001c0001t0001g0161 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.100+4645T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152787887 | ||||||
| chr7:152788025
|
A | C | 1 | a0001c0001t0001g0139 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.100+4783A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152788025 | ||||||
| chr7:152788049
|
C | T | 1 | a0001c0001t0008g0307 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.100+4807C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152788049 | ||||||
| chr7:152788079
|
CACGTCCA others(25): Show |
C | 74 | a0001c0001t0001g0003a0001c0001t0001g0201a0001c0001t0001g0202others(71): Show | 75 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.100+4871_100+4902d others(34): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152788079 | |||||
| chr7:152788175
|
TG | T | 254 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.100+4936delG | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152788175 | |||||
| chr7:152788251
|
C | T | 1 | a0001c0001t0002g0096 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.100+5009C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152788251 | ||||||
| chr7:152788295
|
G | A | 2 | a0001c0001t0001g0238a0001c0001t0001g0268 | 2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.100+5053G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152788295 | ||||||
| chr7:152788299
|
A | G | 9 | a0001c0001t0001g0003a0001c0001t0001g0288a0001c0001t0001g0289others(6): Show | 10 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.100+5057A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152788299 | ||||||
| chr7:152788411
|
G | GT | 83 | a0001c0001t0001g0003a0001c0001t0001g0114a0001c0001t0001g0123others(80): Show | 84 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.100+5187dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152788411 | |||||
| chr7:152788411
|
GT | G | 8 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0298others(5): Show | 8 | HG01952.hp1 HG02145.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.100+5187delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152788411 | |||||
| chr7:152788466
|
C | T | 1 | a0001c0001t0010g0228 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.100+5224C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152788466 | ||||||
| chr7:152788497
|
C | T | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.100+5255C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152788497 | ||||||
| chr7:152788504
|
C | T | 6 | a0001c0001t0001g0302a0001c0001t0002g0157a0001c0001t0002g0158others(3): Show | 6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+5262C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152788504 | ||||||
| chr7:152788662
|
C | T | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.100+5420C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152788662 | ||||||
| chr7:152788769
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+5527C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152788769 | ||||||
| chr7:152788813
|
G | C | 18 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.100+5571G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152788813 | ||||||
| chr7:152788832
|
G | A | 23 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(20): Show | 23 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.100+5590G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152788832 | ||||||
| chr7:152788897
|
C | T | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0254 | 3 | NA18951.hp1 NA19056.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.100+5655C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152788897 | ||||||
| chr7:152788914
|
T | C | 2 | a0001c0001t0001g0114a0001c0001t0001g0143 | 2 | HG00741.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.100+5672T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152788914 | ||||||
| chr7:152788999
|
G | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+5757G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152788999 | ||||||
| chr7:152789000
|
C | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+5758C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789000 | ||||||
| chr7:152789014
|
G | T | 8 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0302others(5): Show | 8 | HG02615.hp1 HG02630.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.100+5772G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789014 | ||||||
| chr7:152789023
|
A | AAAC | 14 | a0001c0001t0001g0277a0001c0001t0002g0006a0001c0001t0002g0007others(11): Show | 14 | HG00738.hp2 HG01074.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.100+5808_100+5810d others(5): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789023 | |||||
| chr7:152789023
|
A | AAACAAC | 106 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(103): Show | 106 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.100+5805_100+5810d others(8): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789023 | |||||
| chr7:152789023
|
A | AAACAACA others(5): Show |
1 | a0001c0001t0008g0307 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.100+5799_100+5810d others(14): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789023 | |||||
| chr7:152789023
|
AAAC | A | 10 | a0001c0001t0001g0022a0001c0001t0001g0108a0001c0001t0001g0111others(7): Show | 10 | HG01081.hp2 HG01192.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.100+5808_100+5810d others(5): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789023 | |||||
| chr7:152789023
|
AAACAAC | A | 6 | a0001c0001t0001g0302a0001c0001t0002g0157a0001c0001t0002g0158others(3): Show | 6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+5805_100+5810d others(8): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789023 | |||||
| chr7:152789041
|
C | CAATA | 7 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0298others(4): Show | 7 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+5801_100+5802i others(6): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789041 | |||||
| chr7:152789043
|
A | ATAAACAG | 17 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(14): Show | 17 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.100+5801_100+5802i others(9): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789043 | ||||||
| chr7:152789043
|
A | G | 1 | a0001c0001t0005g0183 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.100+5801A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789043 | ||||||
| chr7:152789046
|
A | ACAAACAG | 14 | a0001c0001t0001g0003a0001c0001t0001g0239a0001c0001t0001g0240others(11): Show | 15 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.100+5807_100+5808i others(9): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789046 | |||||
| chr7:152789046
|
A | G | 7 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0298others(4): Show | 7 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+5804A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789046 | ||||||
| chr7:152789047
|
C | CA | 39 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.100+5807dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789047 | |||||
| chr7:152789049
|
A | AACAG | 18 | a0001c0001t0001g0201a0001c0001t0001g0207a0001c0001t0001g0224others(15): Show | 18 | HG00597.hp2 HG01884.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.100+5807_100+5808i others(6): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789049 | ||||||
| chr7:152789050
|
C | A | 2 | a0001c0001t0001g0251a0001c0001t0001g0265 | 2 | HG01891.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.100+5808C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789050 | ||||||
| chr7:152789050
|
C | T | 6 | a0001c0001t0001g0302a0001c0001t0002g0157a0001c0001t0002g0158others(3): Show | 6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+5808C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789050 | ||||||
| chr7:152789051
|
A | AAC | 34 | a0001c0001t0001g0003a0001c0001t0001g0201a0001c0001t0001g0207others(31): Show | 35 | HG00099.hp1 HG00597.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.100+5810_100+5811i others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789051 | |||||
| chr7:152789051
|
A | AGC | 39 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.100+5809_100+5810i others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789051 | ||||||
| chr7:152789051
|
A | C | 2 | a0001c0001t0001g0251a0001c0001t0001g0265 | 2 | HG01891.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.100+5809A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789051 | ||||||
| chr7:152789053
|
A | C | 7 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0298others(4): Show | 7 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+5811A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789053 | ||||||
| chr7:152789053
|
A | G | 2 | a0001c0001t0001g0251a0001c0001t0001g0265 | 2 | HG01891.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.100+5811A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789053 | ||||||
| chr7:152789054
|
C | A | 7 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0298others(4): Show | 7 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+5812C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789054 | ||||||
| chr7:152789056
|
G | A | 101 | a0001c0001t0001g0003a0001c0001t0001g0181a0001c0001t0001g0182others(98): Show | 102 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.100+5814G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789056 | ||||||
| chr7:152789063
|
CA | C | 8 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0191others(5): Show | 8 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.100+5824delA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789063 | |||||
| chr7:152789064
|
A | AAAC | 6 | a0001c0001t0001g0302a0001c0001t0002g0157a0001c0001t0002g0158others(3): Show | 6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+5840_100+5842d others(5): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789064 | |||||
| chr7:152789064
|
A | AAC | 91 | a0001c0001t0001g0003a0001c0001t0001g0184a0001c0001t0001g0186others(88): Show | 92 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.100+5823_100+5824i others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789064 | |||||
| chr7:152789064
|
A | AACAACAA others(4): Show |
2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG01099.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.100+5823_100+5824i others(13): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789064 | |||||
| chr7:152789064
|
A | AACAACAA others(7): Show |
1 | a0001c0001t0001g0012 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.100+5823_100+5824i others(16): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789064 | |||||
| chr7:152789064
|
A | AACAACAA others(10): Show |
1 | a0001c0001t0001g0013 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.100+5823_100+5824i others(19): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789064 | |||||
| chr7:152789064
|
AAAC | A | 115 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(112): Show | 115 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.100+5840_100+5842d others(5): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789064 | |||||
| chr7:152789066
|
A | C | 2 | a0001c0001t0001g0259a0001c0001t0002g0070 | 2 | HG00099.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.100+5824A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789066 | ||||||
| chr7:152789067
|
C | A | 2 | a0001c0001t0001g0259a0001c0001t0002g0070 | 2 | HG00099.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.100+5825C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789067 | ||||||
| chr7:152789074
|
A | G | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+5832A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789074 | ||||||
| chr7:152789215
|
A | C | 37 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(34): Show | 37 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.100+5973A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789215 | ||||||
| chr7:152789231
|
A | C | 6 | a0001c0001t0001g0302a0001c0001t0002g0157a0001c0001t0002g0158others(3): Show | 6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+5989A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789231 | ||||||
| chr7:152789261
|
G | A | 92 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(89): Show | 93 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.100+6019G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789261 | ||||||
| chr7:152789284
|
C | T | 7 | a0001c0001t0001g0302a0001c0001t0002g0157a0001c0001t0002g0158others(4): Show | 7 | HG02257.hp1 HG02630.hp2 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+6042C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789284 | ||||||
| chr7:152789348
|
T | C | 105 | a0001c0001t0001g0003a0001c0001t0001g0181a0001c0001t0001g0182others(102): Show | 106 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.100+6106T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789348 | ||||||
| chr7:152789356
|
C | T | 1 | a0001c0001t0002g0157 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.100+6114C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789356 | ||||||
| chr7:152789375
|
C | T | 37 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(34): Show | 37 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.100+6133C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789375 | ||||||
| chr7:152789466
|
G | C | 2 | a0001c0001t0002g0045a0001c0001t0002g0092 | 2 | HG02165.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.100+6224G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789466 | ||||||
| chr7:152789487
|
T | A | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(3): Show | 6 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.100+6245T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789487 | ||||||
| chr7:152789497
|
A | G | 1 | a0001c0001t0001g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.100+6255A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789497 | ||||||
| chr7:152789511
|
A | T | 37 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(34): Show | 37 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.100+6269A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789511 | ||||||
| chr7:152789519
|
G | A | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.100+6277G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789519 | ||||||
| chr7:152789549
|
AT | A | 14 | a0001c0001t0001g0003a0001c0001t0001g0239a0001c0001t0001g0259others(11): Show | 15 | HG00609.hp2 HG01109.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.100+6319delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789549 | |||||
| chr7:152789549
|
ATTT | A | 37 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(34): Show | 37 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.100+6317_100+6319d others(5): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789549 | |||||
| chr7:152789566
|
C | T | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+6324C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789566 | ||||||
| chr7:152789567
|
A | G | 37 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(34): Show | 37 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.100+6325A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789567 | ||||||
| chr7:152789605
|
G | C | 18 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.100+6363G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789605 | ||||||
| chr7:152789613
|
A | G | 1 | a0001c0001t0001g0253 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.100+6371A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789613 | ||||||
| chr7:152789735
|
G | A | 4 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(1): Show | 4 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+6493G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789735 | ||||||
| chr7:152789745
|
C | T | 19 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(16): Show | 19 | HG01099.hp2 HG01106.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.100+6503C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789745 | ||||||
| chr7:152789904
|
T | TA | 4 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(1): Show | 4 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+6669dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789904 | |||||
| chr7:152789914
|
A | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+6672A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789914 | ||||||
| chr7:152789930
|
A | G | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0242others(1): Show | 4 | HG00735.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+6688A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789930 | ||||||
| chr7:152789997
|
C | CT | 92 | a0001c0001t0001g0003a0001c0001t0001g0120a0001c0001t0001g0160others(89): Show | 93 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.100+6777dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789997 | |||||
| chr7:152789997
|
C | CTTT | 17 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(14): Show | 17 | HG00735.hp1 HG01109.hp1 HG02300.hp2 others(14): Show |
intron_variant | MODIFIER | c.100+6775_100+6777d others(5): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789997 | |||||
| chr7:152789997
|
CT | C | 20 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.100+6777delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789997 | |||||
| chr7:152790044
|
G | A | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.100+6802G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152790044 | ||||||
| chr7:152790136
|
A | G | 13 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0298others(10): Show | 13 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.100+6894A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152790136 | ||||||
| chr7:152790254
|
A | G | 19 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(16): Show | 19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.100+7012A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152790254 | ||||||
| chr7:152790312
|
T | A | 1 | a0001c0001t0002g0018 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.100+7070T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152790312 | ||||||
| chr7:152790323
|
C | T | 15 | a0001c0001t0001g0003a0001c0001t0001g0236a0001c0001t0001g0237others(12): Show | 16 | HG00735.hp1 HG01109.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.100+7081C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152790323 | ||||||
| chr7:152790373
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.100+7131G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152790373 | ||||||
| chr7:152790481
|
A | C | 37 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(34): Show | 37 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.100+7239A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152790481 | ||||||
| chr7:152790489
|
A | G | 1 | a0001c0001t0002g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.100+7247A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152790489 | ||||||
| chr7:152790641
|
A | G | 1 | a0001c0001t0002g0054 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.100+7399A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152790641 | ||||||
| chr7:152790869
|
C | T | 13 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0298others(10): Show | 13 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.100+7627C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152790869 | ||||||
| chr7:152790941
|
A | T | 37 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(34): Show | 37 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.100+7699A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152790941 | ||||||
| chr7:152790987
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.100+7745G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152790987 | ||||||
| chr7:152791015
|
CT | C | 17 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(14): Show | 17 | HG01099.hp2 HG01106.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.100+7789delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152791015 | |||||
| chr7:152791156
|
G | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.100+7914G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152791156 | ||||||
| chr7:152791171
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.100+7929C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152791171 | ||||||
| chr7:152791202
|
G | T | 3 | a0001c0001t0001g0210a0001c0001t0001g0215a0001c0001t0001g0221 | 3 | NA18981.hp1 NA18999.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.100+7960G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152791202 | ||||||
| chr7:152791209
|
T | C | 37 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(34): Show | 37 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.100+7967T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152791209 | ||||||
| chr7:152792035
|
G | A | 18 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-8496G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152792035 | ||||||
| chr7:152792138
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.101-8393C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152792138 | ||||||
| chr7:152792305
|
A | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-8226A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152792305 | ||||||
| chr7:152792335
|
G | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0118a0001c0001t0001g0119others(1): Show | 4 | HG01361.hp1 HG01496.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-8196G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152792335 | ||||||
| chr7:152792450
|
T | C | 37 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(34): Show | 37 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.101-8081T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152792450 | ||||||
| chr7:152792471
|
C | A | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG00735.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.101-8060C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152792471 | ||||||
| chr7:152792616
|
G | A | 11 | a0001c0001t0003g0166a0001c0001t0003g0168a0001c0001t0003g0173others(8): Show | 11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.101-7915G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152792616 | ||||||
| chr7:152792709
|
C | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.101-7822C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152792709 | ||||||
| chr7:152792710
|
T | C | 1 | a0001c0001t0002g0078 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.101-7821T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152792710 | ||||||
| chr7:152792768
|
A | G | 19 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(16): Show | 19 | HG01099.hp2 HG01106.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.101-7763A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152792768 | ||||||
| chr7:152792778
|
C | T | 118 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(115): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.101-7753C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152792778 | ||||||
| chr7:152792869
|
A | C | 1 | a0001c0001t0002g0004 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.101-7662A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152792869 | ||||||
| chr7:152792892
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.101-7639A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152792892 | ||||||
| chr7:152792940
|
T | TAA | 7 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0298others(4): Show | 7 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.101-7591_101-7590i others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152792940 | ||||||
| chr7:152792964
|
C | CT | 25 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(22): Show | 25 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.101-7558dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152792964 | |||||
| chr7:152792981
|
A | G | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.101-7550A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152792981 | ||||||
| chr7:152793022
|
A | AT | 10 | a0001c0001t0001g0120a0001c0001t0001g0263a0001c0001t0001g0277others(7): Show | 10 | HG00423.hp1 HG01081.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.101-7489dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152793022 | |||||
| chr7:152793022
|
AT | A | 41 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(38): Show | 41 | HG01070.hp2 HG01099.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.101-7489delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152793022 | |||||
| chr7:152793084
|
A | G | 1 | a0001c0001t0002g0156 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.101-7447A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152793084 | ||||||
| chr7:152793166
|
T | C | 59 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(56): Show | 59 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.101-7365T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152793166 | ||||||
| chr7:152793174
|
C | CT | 247 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.101-7347dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152793174 | |||||
| chr7:152793201
|
G | GT | 254 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.101-7327dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152793201 | |||||
| chr7:152793296
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.101-7235A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152793296 | ||||||
| chr7:152793328
|
GT | G | 226 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(223): Show | 228 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(225): Show |
intron_variant | MODIFIER | c.101-7190delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152793328 | |||||
| chr7:152793329
|
T | C | 1 | a0001c0001t0002g0046 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.101-7202T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152793329 | ||||||
| chr7:152793363
|
C | G | 18 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-7168C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152793363 | ||||||
| chr7:152793490
|
T | A | 2 | a0001c0001t0002g0026a0001c0001t0002g0065 | 2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.101-7041T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152793490 | ||||||
| chr7:152793510
|
G | A | 18 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-7021G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152793510 | ||||||
| chr7:152793552
|
G | T | 1 | a0001c0001t0003g0279 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.101-6979G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152793552 | ||||||
| chr7:152793605
|
T | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0269 | 2 | HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.101-6926T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152793605 | ||||||
| chr7:152793736
|
T | C | 1 | a0001c0001t0002g0072 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.101-6795T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152793736 | ||||||
| chr7:152793884
|
A | G | 18 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-6647A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152793884 | ||||||
| chr7:152793926
|
GGAGGAGC others(7): Show |
G | 3 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0280 | 3 | HG01167.hp2 HG01169.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.101-6604_101-6591d others(16): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152793926 | ||||||
| chr7:152793952
|
T | C | 1 | a0001c0001t0001g0269 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.101-6579T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152793952 | ||||||
| chr7:152794109
|
T | C | 2 | a0001c0001t0002g0025a0001c0001t0002g0071 | 2 | HG02735.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.101-6422T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152794109 | ||||||
| chr7:152794222
|
A | G | 4 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0065others(1): Show | 4 | HG02280.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-6309A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152794222 | ||||||
| chr7:152794385
|
G | T | 243 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(240): Show | 245 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.101-6146G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152794385 | ||||||
| chr7:152794461
|
C | A | 118 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(115): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.101-6070C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152794461 | ||||||
| chr7:152794561
|
C | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.101-5970C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152794561 | ||||||
| chr7:152794722
|
A | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.101-5809A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152794722 | ||||||
| chr7:152794750
|
G | A | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-5781G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152794750 | ||||||
| chr7:152794768
|
G | C | 18 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-5763G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152794768 | ||||||
| chr7:152794793
|
A | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.101-5738A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152794793 | ||||||
| chr7:152794830
|
C | G | 19 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(16): Show | 19 | HG01099.hp2 HG01106.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.101-5701C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152794830 | ||||||
| chr7:152794925
|
A | G | 1 | a0001c0001t0001g0161 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.101-5606A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152794925 | ||||||
| chr7:152794954
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.101-5577C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152794954 | ||||||
| chr7:152795031
|
A | ACT | 110 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(107): Show | 110 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.101-5495_101-5494d others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152795031 | |||||
| chr7:152795036
|
C | CTT | 18 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-5480_101-5479d others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152795036 | |||||
| chr7:152795036
|
CT | C | 6 | a0001c0001t0001g0139a0001c0001t0001g0216a0001c0001t0001g0242others(3): Show | 6 | HG01167.hp2 HG02451.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.101-5479delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152795036 | |||||
| chr7:152795037
|
T | TC | 7 | a0001c0001t0001g0259a0001c0001t0001g0278a0001c0001t0002g0075others(4): Show | 7 | HG00558.hp1 HG01167.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.101-5494_101-5493i others(3): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152795037 | ||||||
| chr7:152795042
|
T | G | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(3): Show | 6 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.101-5489T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152795042 | ||||||
| chr7:152795319
|
T | A | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.101-5212T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152795319 | ||||||
| chr7:152795580
|
G | A | 6 | a0001c0001t0001g0302a0001c0001t0002g0157a0001c0001t0002g0158others(3): Show | 6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.101-4951G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152795580 | ||||||
| chr7:152795603
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.101-4928C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152795603 | ||||||
| chr7:152795771
|
T | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-4760T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152795771 | ||||||
| chr7:152795846
|
G | GT | 103 | a0001c0001t0001g0003a0001c0001t0001g0120a0001c0001t0001g0201others(100): Show | 105 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.101-4671dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152795846 | |||||
| chr7:152795866
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.101-4665C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152795866 | ||||||
| chr7:152796073
|
G | C | 1 | a0001c0001t0002g0080 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.101-4458G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796073 | ||||||
| chr7:152796140
|
C | T | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-4391C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796140 | ||||||
| chr7:152796154
|
C | G | 5 | a0001c0001t0002g0007a0001c0001t0002g0155a0001c0001t0002g0156others(2): Show | 5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-4377C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796154 | ||||||
| chr7:152796183
|
C | T | 2 | a0001c0001t0006g0185a0001c0001t0006g0194 | 2 | NA18948.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.101-4348C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796183 | ||||||
| chr7:152796303
|
A | G | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0242others(1): Show | 4 | HG00735.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-4228A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796303 | ||||||
| chr7:152796380
|
A | T | 1 | a0001c0001t0002g0007 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.101-4151A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796380 | ||||||
| chr7:152796421
|
G | A | 155 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(152): Show | 155 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.101-4110G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796421 | ||||||
| chr7:152796431
|
A | G | 8 | a0001c0001t0001g0296a0001c0001t0002g0002a0001c0001t0002g0019others(5): Show | 9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.101-4100A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796431 | ||||||
| chr7:152796447
|
A | G | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.101-4084A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796447 | ||||||
| chr7:152796450
|
A | G | 6 | a0001c0001t0001g0302a0001c0001t0002g0157a0001c0001t0002g0158others(3): Show | 6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.101-4081A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796450 | ||||||
| chr7:152796550
|
A | G | 1 | a0001c0001t0002g0006 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.101-3981A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796550 | ||||||
| chr7:152796644
|
A | T | 118 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(115): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.101-3887A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796644 | ||||||
| chr7:152796716
|
G | C | 118 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(115): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.101-3815G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796716 | ||||||
| chr7:152796731
|
T | C | 118 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(115): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.101-3800T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796731 | ||||||
| chr7:152796812
|
C | T | 1 | a0001c0001t0002g0037 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.101-3719C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796812 | ||||||
| chr7:152796860
|
GT | G | 19 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0146others(16): Show | 19 | HG00423.hp2 HG00597.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.101-3633delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152796860 | |||||
| chr7:152796860
|
GTT | G | 77 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0118others(74): Show | 77 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.101-3634_101-3633d others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152796860 | |||||
| chr7:152796860
|
GTTT | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(87): Show | 93 | HG00423.hp1 HG00642.hp2 HG01070.hp1 others(90): Show |
intron_variant | MODIFIER | c.101-3635_101-3633d others(5): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152796860 | |||||
| chr7:152796860
|
GTTTT | G | 103 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0200others(100): Show | 103 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.101-3636_101-3633d others(6): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152796860 | |||||
| chr7:152796860
|
GTTTTTTT others(8): Show |
G | 1 | a0001c0002t0001g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.101-3647_101-3633d others(17): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152796860 | |||||
| chr7:152796860
|
GTTTTTTT others(16): Show |
G | 1 | a0001c0001t0001g0269 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.101-3655_101-3633d others(25): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152796860 | |||||
| chr7:152796860
|
GTTTTTTT others(17): Show |
G | 1 | a0001c0001t0006g0194 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.101-3656_101-3633d others(26): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152796860 | |||||
| chr7:152796862
|
T | G | 2 | a0001c0001t0001g0299a0001c0001t0001g0300 | 2 | HG01952.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.101-3669T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796862 | ||||||
| chr7:152796863
|
T | G | 1 | a0001c0001t0001g0298 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.101-3668T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796863 | ||||||
| chr7:152796864
|
T | G | 1 | a0001c0001t0001g0304 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.101-3667T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796864 | ||||||
| chr7:152796871
|
T | G | 13 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0121others(10): Show | 13 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.101-3660T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796871 | ||||||
| chr7:152796872
|
T | G | 25 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0120others(22): Show | 26 | HG00642.hp2 HG01074.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.101-3659T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796872 | ||||||
| chr7:152796874
|
T | G | 1 | a0001c0001t0001g0230 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.101-3657T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796874 | ||||||
| chr7:152796875
|
T | G | 13 | a0001c0001t0001g0200a0001c0001t0001g0221a0001c0001t0001g0236others(10): Show | 13 | HG00099.hp1 HG00423.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.101-3656T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796875 | ||||||
| chr7:152796876
|
T | G | 59 | a0001c0001t0001g0003a0001c0001t0001g0201a0001c0001t0001g0203others(56): Show | 60 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.101-3655T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796876 | ||||||
| chr7:152796877
|
T | G | 28 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(25): Show | 29 | HG01070.hp1 HG01074.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.101-3654T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796877 | ||||||
| chr7:152796878
|
T | G | 6 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0187others(3): Show | 6 | HG02615.hp1 HG02723.hp2 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.101-3653T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796878 | ||||||
| chr7:152796879
|
T | G | 25 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0190others(22): Show | 25 | HG00423.hp1 HG01109.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.101-3652T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796879 | ||||||
| chr7:152796880
|
T | G | 103 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(100): Show | 103 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.101-3651T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796880 | ||||||
| chr7:152796881
|
T | G | 2 | a0001c0001t0002g0063a0001c0001t0002g0084 | 2 | HG01081.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.101-3650T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796881 | ||||||
| chr7:152796883
|
T | G | 5 | a0001c0001t0002g0007a0001c0001t0002g0155a0001c0001t0002g0156others(2): Show | 5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-3648T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796883 | ||||||
| chr7:152796884
|
T | G | 2 | a0001c0001t0002g0077a0001c0001t0002g0078 | 2 | HG02074.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.101-3647T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796884 | ||||||
| chr7:152796885
|
T | G | 3 | a0001c0001t0001g0259a0001c0001t0002g0028a0001c0001t0002g0067 | 3 | HG01256.hp2 HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.101-3646T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796885 | ||||||
| chr7:152796886
|
T | G | 1 | a0001c0001t0001g0196 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.101-3645T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796886 | ||||||
| chr7:152796907
|
G | A | 155 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(152): Show | 155 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.101-3624G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796907 | ||||||
| chr7:152797062
|
T | G | 1 | a0001c0001t0001g0238 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.101-3469T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152797062 | ||||||
| chr7:152797101
|
A | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0113others(4): Show | 8 | HG00741.hp1 HG01074.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.101-3430A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152797101 | ||||||
| chr7:152797216
|
A | G | 1 | a0001c0001t0001g0298 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.101-3315A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152797216 | ||||||
| chr7:152797357
|
G | A | 5 | a0001c0001t0002g0007a0001c0001t0002g0155a0001c0001t0002g0156others(2): Show | 5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-3174G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152797357 | ||||||
| chr7:152797460
|
T | C | 1 | a0001c0001t0002g0079 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.101-3071T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152797460 | ||||||
| chr7:152797476
|
G | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-3055G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152797476 | ||||||
| chr7:152797573
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.101-2958A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152797573 | ||||||
| chr7:152797580
|
G | A | 4 | a0001c0001t0001g0296a0001c0001t0002g0002a0001c0001t0002g0179others(1): Show | 5 | HG01884.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-2951G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152797580 | ||||||
| chr7:152797643
|
T | C | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.101-2888T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152797643 | ||||||
| chr7:152797866
|
C | CTT | 18 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-2656_101-2655d others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152797866 | |||||
| chr7:152797892
|
A | T | 9 | a0001c0001t0001g0003a0001c0001t0001g0288a0001c0001t0001g0289others(6): Show | 10 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.101-2639A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152797892 | ||||||
| chr7:152798199
|
C | T | 254 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.101-2332C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152798199 | ||||||
| chr7:152798442
|
G | A | 17 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(14): Show | 17 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.101-2089G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152798442 | ||||||
| chr7:152798583
|
T | TCCAAAAA others(9): Show |
2 | a0001c0001t0002g0171a0001c0001t0002g0172 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.101-1944_101-1929d others(18): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152798583 | |||||
| chr7:152798847
|
T | A | 1 | a0001c0001t0001g0263 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.101-1684T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152798847 | ||||||
| chr7:152799126
|
T | C | 5 | a0001c0001t0002g0007a0001c0001t0002g0155a0001c0001t0002g0156others(2): Show | 5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-1405T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152799126 | ||||||
| chr7:152799295
|
G | A | 254 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.101-1236G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152799295 | ||||||
| chr7:152799314
|
C | A | 18 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-1217C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152799314 | ||||||
| chr7:152799507
|
C | T | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.101-1024C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152799507 | ||||||
| chr7:152799511
|
AATT | A | 6 | a0001c0001t0001g0302a0001c0001t0002g0157a0001c0001t0002g0158others(3): Show | 6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.101-1009_101-1007d others(5): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152799511 | |||||
| chr7:152799534
|
T | A | 254 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.101-997T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152799534 | ||||||
| chr7:152799541
|
C | T | 5 | a0001c0001t0002g0007a0001c0001t0002g0155a0001c0001t0002g0156others(2): Show | 5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-990C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152799541 | ||||||
| chr7:152799561
|
T | TA | 74 | a0001c0001t0001g0003a0001c0001t0001g0201a0001c0001t0001g0202others(71): Show | 75 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.101-967dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152799561 | |||||
| chr7:152799571
|
G | T | 155 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(152): Show | 155 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.101-960G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152799571 | ||||||
| chr7:152799581
|
T | A | 1 | a0001c0001t0001g0022 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.101-950T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152799581 | ||||||
| chr7:152799594
|
A | G | 3 | a0001c0001t0002g0040a0001c0001t0002g0088a0001c0001t0002g0093 | 3 | NA18956.hp2 NA19062.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.101-937A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152799594 | ||||||
| chr7:152799595
|
T | C | 235 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(232): Show | 236 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.101-936T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152799595 | ||||||
| chr7:152799630
|
A | G | 57 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(54): Show | 57 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.101-901A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152799630 | ||||||
| chr7:152799701
|
G | A | 118 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(115): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.101-830G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152799701 | ||||||
| chr7:152799773
|
A | G | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0242others(1): Show | 4 | HG00735.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-758A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152799773 | ||||||
| chr7:152799890
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.101-641A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152799890 | ||||||
| chr7:152800064
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.101-467T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152800064 | ||||||
| chr7:152800314
|
C | A | 1 | a0001c0001t0002g0155 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.101-217C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152800314 | ||||||
| chr7:152800323
|
A | T | 1 | a0001c0001t0001g0134 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.101-208A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152800323 | ||||||
| chr7:152800758
|
A | G | 1 | a0001c0001t0001g0304 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.225+103A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 3/11 | chr7 | 152800758 | ||||||
| chr7:152800816
|
T | TA | 9 | a0001c0001t0001g0003a0001c0001t0001g0288a0001c0001t0001g0289others(6): Show | 10 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.225+162dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 152800816 | |||||
| chr7:152800885
|
G | A | 118 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(115): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.225+230G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 3/11 | chr7 | 152800885 | ||||||
| chr7:152800891
|
C | T | 59 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(56): Show | 59 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.225+236C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 3/11 | chr7 | 152800891 | ||||||
| chr7:152801014
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.225+359T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 3/11 | chr7 | 152801014 | ||||||
| chr7:152801023
|
T | C | 6 | a0001c0001t0001g0302a0001c0001t0002g0157a0001c0001t0002g0158others(3): Show | 6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.225+368T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 3/11 | chr7 | 152801023 | ||||||
| chr7:152801121
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.225+466C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 3/11 | chr7 | 152801121 | ||||||
| chr7:152801143
|
C | T | 1 | a0001c0001t0001g0302 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.226-478C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 3/11 | chr7 | 152801143 | ||||||
| chr7:152801226
|
C | T | 118 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(115): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.226-395C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 3/11 | chr7 | 152801226 | ||||||
| chr7:152801278
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.226-343C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 3/11 | chr7 | 152801278 | ||||||
| chr7:152801297
|
T | C | 155 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(152): Show | 155 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.226-324T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 3/11 | chr7 | 152801297 | ||||||
| chr7:152801345
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.226-276G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 3/11 | chr7 | 152801345 | ||||||
| chr7:152801348
|
G | A | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.226-273G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 3/11 | chr7 | 152801348 | ||||||
| chr7:152801466
|
T | G | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.226-155T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 3/11 | chr7 | 152801466 | ||||||
| chr7:152801899
|
A | AG | 155 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(152): Show | 155 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.336+171dupG | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152801899 | |||||
| chr7:152801935
|
A | T | 1 | a0001c0001t0001g0182 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.336+204A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152801935 | ||||||
| chr7:152801993
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.336+262G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152801993 | ||||||
| chr7:152802279
|
A | G | 254 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.336+548A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152802279 | ||||||
| chr7:152802409
|
T | C | 1 | a0001c0001t0008g0307 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.336+678T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152802409 | ||||||
| chr7:152802463
|
G | A | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.336+732G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152802463 | ||||||
| chr7:152802737
|
G | A | 96 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0225others(93): Show | 96 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.336+1006G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152802737 | ||||||
| chr7:152802888
|
C | T | 6 | a0001c0001t0001g0123a0001c0001t0001g0129a0001c0001t0001g0131others(3): Show | 6 | HG00544.hp2 HG02074.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.336+1157C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152802888 | ||||||
| chr7:152802968
|
A | G | 118 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(115): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.336+1237A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152802968 | ||||||
| chr7:152803127
|
G | T | 2 | a0001c0001t0001g0299a0001c0001t0001g0304 | 2 | HG01952.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.336+1396G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152803127 | ||||||
| chr7:152803128
|
C | T | 2 | a0001c0001t0001g0299a0001c0001t0001g0304 | 2 | HG01952.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.336+1397C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152803128 | ||||||
| chr7:152803178
|
T | C | 5 | a0001c0001t0002g0007a0001c0001t0002g0155a0001c0001t0002g0156others(2): Show | 5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.336+1447T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152803178 | ||||||
| chr7:152803217
|
A | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.336+1486A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152803217 | ||||||
| chr7:152803218
|
A | G | 13 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0298others(10): Show | 13 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.336+1487A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152803218 | ||||||
| chr7:152803248
|
A | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.336+1517A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152803248 | ||||||
| chr7:152803299
|
T | C | 118 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(115): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.336+1568T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152803299 | ||||||
| chr7:152803602
|
G | A | 1 | a0001c0001t0002g0021 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.336+1871G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152803602 | ||||||
| chr7:152803854
|
A | G | 118 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(115): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.336+2123A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152803854 | ||||||
| chr7:152803928
|
G | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.336+2197G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152803928 | ||||||
| chr7:152804146
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.336+2415G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152804146 | ||||||
| chr7:152804229
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.336+2498C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152804229 | ||||||
| chr7:152804286
|
G | A | 156 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(153): Show | 156 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.336+2555G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152804286 | ||||||
| chr7:152804286
|
G | C | 2 | a0001c0001t0002g0156a0001c0001t0002g0165 | 2 | HG01074.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.336+2555G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152804286 | ||||||
| chr7:152804574
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.336+2843G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152804574 | ||||||
| chr7:152804592
|
G | A | 1 | a0001c0001t0002g0082 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.336+2861G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152804592 | ||||||
| chr7:152804740
|
G | A | 118 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(115): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.336+3009G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152804740 | ||||||
| chr7:152804791
|
G | T | 156 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(153): Show | 156 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.336+3060G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152804791 | ||||||
| chr7:152804835
|
C | T | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0242others(1): Show | 4 | HG00735.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.336+3104C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152804835 | ||||||
| chr7:152804882
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.336+3151C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152804882 | ||||||
| chr7:152804893
|
A | G | 118 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(115): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.336+3162A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152804893 | ||||||
| chr7:152804986
|
C | T | 118 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(115): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.336+3255C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152804986 | ||||||
| chr7:152805003
|
ACTCATGG others(8): Show |
A | 19 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(16): Show | 19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.336+3274_336+3288d others(17): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152805003 | |||||
| chr7:152805020
|
G | A | 1 | a0001c0001t0002g0101 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.336+3289G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152805020 | ||||||
| chr7:152805051
|
G | A | 19 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(16): Show | 19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.336+3320G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152805051 | ||||||
| chr7:152805109
|
TG | T | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0242others(1): Show | 4 | HG00735.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.336+3382delG | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152805109 | |||||
| chr7:152805112
|
G | T | 9 | a0001c0001t0001g0003a0001c0001t0001g0288a0001c0001t0001g0289others(6): Show | 10 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.336+3381G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152805112 | ||||||
| chr7:152805140
|
T | C | 2 | a0001c0001t0001g0241a0001c0001t0001g0282 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.336+3409T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152805140 | ||||||
| chr7:152805476
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.336+3745C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152805476 | ||||||
| chr7:152805480
|
C | T | 1 | a0001c0001t0001g0289 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.336+3749C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152805480 | ||||||
| chr7:152805514
|
A | T | 1 | a0001c0001t0002g0048 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.336+3783A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152805514 | ||||||
| chr7:152805622
|
A | C | 57 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(54): Show | 57 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.336+3891A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152805622 | ||||||
| chr7:152805803
|
C | T | 6 | a0001c0001t0001g0302a0001c0001t0002g0157a0001c0001t0002g0158others(3): Show | 6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.336+4072C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152805803 | ||||||
| chr7:152805937
|
GGGTT | G | 13 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0298others(10): Show | 13 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.336+4211_336+4214d others(6): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152805937 | |||||
| chr7:152806059
|
A | G | 1 | a0001c0001t0001g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.336+4328A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152806059 | ||||||
| chr7:152806091
|
T | C | 96 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0225others(93): Show | 96 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.336+4360T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152806091 | ||||||
| chr7:152806148
|
C | T | 5 | a0001c0001t0002g0007a0001c0001t0002g0155a0001c0001t0002g0156others(2): Show | 5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.336+4417C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152806148 | ||||||
| chr7:152806183
|
T | C | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.336+4452T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152806183 | ||||||
| chr7:152806408
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.336+4677C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152806408 | ||||||
| chr7:152806415
|
G | A | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.336+4684G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152806415 | ||||||
| chr7:152806545
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.336+4814C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152806545 | ||||||
| chr7:152806581
|
T | G | 58 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(55): Show | 58 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.336+4850T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152806581 | ||||||
| chr7:152806671
|
C | G | 1 | a0001c0001t0001g0269 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.336+4940C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152806671 | ||||||
| chr7:152806672
|
A | AAGTCTAC others(6): Show |
13 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0298others(10): Show | 13 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.336+4949_336+4961d others(15): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152806672 | |||||
| chr7:152806692
|
C | A | 1 | a0001c0001t0002g0069 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.336+4961C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152806692 | ||||||
| chr7:152806927
|
T | C | 1 | a0001c0001t0002g0075 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.336+5196T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152806927 | ||||||
| chr7:152807218
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.336+5487T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152807218 | ||||||
| chr7:152807326
|
A | G | 2 | a0001c0001t0002g0026a0001c0001t0002g0065 | 2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.336+5595A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152807326 | ||||||
| chr7:152807472
|
A | G | 1 | a0001c0005t0001g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.336+5741A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152807472 | ||||||
| chr7:152807619
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.336+5888C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152807619 | ||||||
| chr7:152807806
|
G | A | 1 | a0001c0001t0002g0087 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.336+6075G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152807806 | ||||||
| chr7:152808171
|
A | G | 1 | a0001c0001t0002g0028 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.337-6379A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152808171 | ||||||
| chr7:152808247
|
C | T | 74 | a0001c0001t0001g0003a0001c0001t0001g0201a0001c0001t0001g0202others(71): Show | 75 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.337-6303C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152808247 | ||||||
| chr7:152808311
|
T | C | 9 | a0001c0001t0001g0003a0001c0001t0001g0288a0001c0001t0001g0289others(6): Show | 10 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.337-6239T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152808311 | ||||||
| chr7:152808376
|
A | G | 1 | a0001c0001t0002g0155 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.337-6174A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152808376 | ||||||
| chr7:152808433
|
C | T | 230 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.337-6117C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152808433 | ||||||
| chr7:152808565
|
A | G | 1 | a0001c0001t0002g0088 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.337-5985A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152808565 | ||||||
| chr7:152808609
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.337-5941C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152808609 | ||||||
| chr7:152808986
|
T | C | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.337-5564T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152808986 | ||||||
| chr7:152809052
|
G | A | 1 | a0001c0001t0001g0182 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.337-5498G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152809052 | ||||||
| chr7:152809099
|
G | A | 4 | a0001c0001t0002g0040a0001c0001t0002g0088a0001c0001t0002g0093others(1): Show | 4 | NA18956.hp2 NA19062.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.337-5451G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152809099 | ||||||
| chr7:152809284
|
C | T | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0242others(1): Show | 4 | HG00735.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.337-5266C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152809284 | ||||||
| chr7:152809306
|
A | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0288a0001c0001t0001g0291others(3): Show | 7 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.337-5244A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152809306 | ||||||
| chr7:152809404
|
G | A | 2 | a0001c0001t0001g0238a0001c0001t0001g0268 | 2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.337-5146G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152809404 | ||||||
| chr7:152809547
|
T | G | 119 | a0001c0001t0001g0011a0001c0001t0001g0200a0001c0001t0001g0213others(116): Show | 119 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.337-5003T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152809547 | ||||||
| chr7:152809583
|
C | A | 1 | a0001c0001t0001g0251 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.337-4967C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152809583 | ||||||
| chr7:152809634
|
C | T | 4 | a0001c0001t0001g0296a0001c0001t0002g0002a0001c0001t0002g0179others(1): Show | 5 | HG01884.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.337-4916C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152809634 | ||||||
| chr7:152809646
|
A | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.337-4904A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152809646 | ||||||
| chr7:152809688
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.337-4862A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152809688 | ||||||
| chr7:152809774
|
C | A | 9 | a0001c0001t0001g0003a0001c0001t0001g0288a0001c0001t0001g0289others(6): Show | 10 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.337-4776C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152809774 | ||||||
| chr7:152809785
|
C | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.337-4765C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152809785 | ||||||
| chr7:152809812
|
A | T | 1 | a0001c0001t0001g0154 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.337-4738A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152809812 | ||||||
| chr7:152809915
|
CT | C | 156 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(153): Show | 156 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.337-4625delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152809915 | |||||
| chr7:152810014
|
A | C | 2 | a0001c0001t0002g0156a0001c0001t0002g0165 | 2 | HG01074.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.337-4536A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810014 | ||||||
| chr7:152810065
|
C | T | 12 | a0001c0001t0001g0201a0001c0001t0001g0239a0001c0001t0001g0240others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.337-4485C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810065 | ||||||
| chr7:152810066
|
G | A | 1 | a0001c0001t0009g0142 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.337-4484G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810066 | ||||||
| chr7:152810138
|
C | T | 1 | a0001c0002t0001g0209 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.337-4412C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810138 | ||||||
| chr7:152810263
|
C | T | 74 | a0001c0001t0001g0003a0001c0001t0001g0201a0001c0001t0001g0202others(71): Show | 75 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.337-4287C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810263 | ||||||
| chr7:152810271
|
T | C | 2 | a0001c0001t0002g0171a0001c0001t0002g0172 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.337-4279T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810271 | ||||||
| chr7:152810273
|
A | G | 2 | a0001c0001t0002g0171a0001c0001t0002g0172 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.337-4277A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810273 | ||||||
| chr7:152810364
|
C | T | 19 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(16): Show | 19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.337-4186C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810364 | ||||||
| chr7:152810408
|
G | GT | 28 | a0001c0001t0001g0011a0001c0001t0001g0111a0001c0001t0001g0113others(25): Show | 28 | HG00597.hp1 HG00642.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.337-4122dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152810408 | |||||
| chr7:152810420
|
T | TG | 7 | a0001c0001t0001g0003a0001c0001t0001g0288a0001c0001t0001g0291others(4): Show | 8 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.337-4130_337-4129i others(3): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810420 | ||||||
| chr7:152810423
|
T | G | 10 | a0001c0001t0001g0003a0001c0001t0001g0207a0001c0001t0001g0247others(7): Show | 11 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.337-4127T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810423 | ||||||
| chr7:152810423
|
T | TG | 13 | a0001c0001t0001g0293a0001c0001t0002g0052a0001c0001t0002g0061others(10): Show | 13 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.337-4127_337-4126i others(3): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810423 | ||||||
| chr7:152810426
|
T | G | 94 | a0001c0001t0001g0003a0001c0001t0001g0181a0001c0001t0001g0182others(91): Show | 95 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.337-4124T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810426 | ||||||
| chr7:152810426
|
T | TG | 108 | a0001c0001t0001g0202a0001c0001t0001g0205a0001c0001t0001g0206others(105): Show | 109 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.337-4124_337-4123i others(3): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810426 | ||||||
| chr7:152810426
|
T | TTG | 25 | a0001c0001t0001g0277a0001c0001t0001g0302a0001c0001t0002g0020others(22): Show | 25 | HG00423.hp1 HG00558.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.337-4123_337-4122i others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152810426 | |||||
| chr7:152810429
|
G | T | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(5): Show | 8 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.337-4121G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810429 | ||||||
| chr7:152810481
|
A | G | 156 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(153): Show | 156 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.337-4069A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810481 | ||||||
| chr7:152810524
|
C | T | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.337-4026C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810524 | ||||||
| chr7:152810588
|
G | C | 38 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(35): Show | 38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.337-3962G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810588 | ||||||
| chr7:152810683
|
C | T | 2 | a0001c0001t0001g0299a0001c0001t0001g0304 | 2 | HG01952.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.337-3867C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810683 | ||||||
| chr7:152810745
|
T | C | 118 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(115): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.337-3805T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810745 | ||||||
| chr7:152810903
|
C | CA | 15 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(12): Show | 15 | HG01099.hp2 HG01106.hp2 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.337-3629dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152810903 | |||||
| chr7:152810903
|
CA | C | 13 | a0001c0001t0001g0003a0001c0001t0001g0129a0001c0001t0001g0148others(10): Show | 14 | HG00544.hp2 HG01074.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.337-3629delA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152810903 | |||||
| chr7:152810969
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.337-3581C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810969 | ||||||
| chr7:152811372
|
G | A | 19 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(16): Show | 19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.337-3178G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152811372 | ||||||
| chr7:152811462
|
C | T | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.337-3088C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152811462 | ||||||
| chr7:152811580
|
C | A | 8 | a0001c0001t0001g0296a0001c0001t0002g0002a0001c0001t0002g0019others(5): Show | 9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.337-2970C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152811580 | ||||||
| chr7:152811586
|
A | G | 19 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(16): Show | 19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.337-2964A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152811586 | ||||||
| chr7:152811955
|
A | T | 118 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(115): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.337-2595A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152811955 | ||||||
| chr7:152812019
|
C | CTTTT | 6 | a0001c0001t0001g0003a0001c0001t0001g0268a0001c0001t0001g0291others(3): Show | 7 | HG01109.hp2 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.337-2505_337-2502d others(6): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | |||||
| chr7:152812019
|
C | CTTTTT | 8 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0292others(5): Show | 8 | HG01074.hp2 HG02055.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.337-2506_337-2502d others(7): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | |||||
| chr7:152812019
|
C | CTTTTTT | 5 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0242others(2): Show | 6 | HG00735.hp1 HG02451.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.337-2507_337-2502d others(8): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | |||||
| chr7:152812019
|
C | CTTTTTTT | 22 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0001t0001g0218others(19): Show | 22 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.337-2508_337-2502d others(9): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | |||||
| chr7:152812019
|
C | CTTTTTTT others(1): Show |
25 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0205others(22): Show | 25 | HG00423.hp2 HG01071.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.337-2509_337-2502d others(10): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | |||||
| chr7:152812019
|
C | CTTTTTTT others(2): Show |
8 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0220others(5): Show | 8 | HG00597.hp2 HG02027.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.337-2510_337-2502d others(11): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | |||||
| chr7:152812019
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0001g0201a0001c0001t0001g0254 | 2 | HG02258.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.337-2511_337-2502d others(12): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | |||||
| chr7:152812019
|
C | CTTTTTTT others(4): Show |
4 | a0001c0001t0001g0222a0001c0001t0001g0235a0001c0001t0001g0240others(1): Show | 4 | HG00642.hp1 HG03139.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.337-2512_337-2502d others(13): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | |||||
| chr7:152812019
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0003g0174a0001c0001t0003g0286 | 2 | HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.337-2513_337-2502d others(14): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | |||||
| chr7:152812019
|
C | CTTTTTTT others(6): Show |
3 | a0001c0001t0003g0166a0001c0001t0003g0279a0001c0001t0004g0169 | 3 | HG02486.hp2 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.337-2514_337-2502d others(15): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | |||||
| chr7:152812019
|
C | CTTTTTTT others(7): Show |
2 | a0001c0001t0004g0170a0001c0001t0004g0176 | 2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.337-2515_337-2502d others(16): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | |||||
| chr7:152812019
|
CT | C | 43 | a0001c0001t0001g0001a0001c0001t0001g0108a0001c0001t0001g0110others(40): Show | 44 | HG00438.hp2 HG00741.hp1 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.337-2502delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | |||||
| chr7:152812019
|
CTT | C | 6 | a0001c0001t0001g0139a0001c0001t0001g0152a0001c0001t0001g0217others(3): Show | 6 | HG01952.hp1 HG02145.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.337-2503_337-2502d others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | |||||
| chr7:152812019
|
CTTTTTTT others(1): Show |
C | 91 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0225others(88): Show | 91 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.337-2509_337-2502d others(10): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | |||||
| chr7:152812019
|
CTTTTTTT others(2): Show |
C | 27 | a0001c0001t0001g0200a0001c0001t0002g0023a0001c0001t0002g0024others(24): Show | 27 | HG00099.hp1 HG00738.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.337-2510_337-2502d others(11): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | |||||
| chr7:152812019
|
CTTTTTTT others(3): Show |
C | 16 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(13): Show | 16 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.337-2511_337-2502d others(12): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | |||||
| chr7:152812019
|
CTTTTTTT others(9): Show |
C | 4 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0177others(1): Show | 4 | HG01361.hp2 HG01934.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.337-2517_337-2502d others(18): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | |||||
| chr7:152812034
|
T | C | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.337-2516T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812034 | ||||||
| chr7:152812054
|
G | A | 1 | a0001c0001t0002g0060 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.337-2496G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812054 | ||||||
| chr7:152812061
|
T | C | 118 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(115): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.337-2489T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812061 | ||||||
| chr7:152812064
|
T | A | 3 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0176 | 3 | HG01891.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.337-2486T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812064 | ||||||
| chr7:152812093
|
C | T | 118 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(115): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.337-2457C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812093 | ||||||
| chr7:152812126
|
G | A | 5 | a0001c0001t0002g0007a0001c0001t0002g0155a0001c0001t0002g0156others(2): Show | 5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.337-2424G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812126 | ||||||
| chr7:152812149
|
G | A | 118 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(115): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.337-2401G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812149 | ||||||
| chr7:152812196
|
A | G | 17 | a0001c0001t0001g0200a0001c0001t0002g0023a0001c0001t0002g0024others(14): Show | 17 | HG00099.hp1 HG00738.hp2 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.337-2354A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812196 | ||||||
| chr7:152812228
|
A | C | 124 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(121): Show | 124 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.337-2322A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812228 | ||||||
| chr7:152812238
|
T | C | 124 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(121): Show | 124 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.337-2312T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812238 | ||||||
| chr7:152812273
|
C | T | 19 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(16): Show | 19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.337-2277C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812273 | ||||||
| chr7:152812320
|
C | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.337-2230C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812320 | ||||||
| chr7:152812349
|
C | A | 8 | a0001c0001t0001g0296a0001c0001t0002g0002a0001c0001t0002g0019others(5): Show | 9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.337-2201C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812349 | ||||||
| chr7:152812353
|
A | G | 129 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(126): Show | 129 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.337-2197A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812353 | ||||||
| chr7:152812377
|
T | C | 1 | a0001c0001t0001g0269 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.337-2173T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812377 | ||||||
| chr7:152812454
|
A | T | 1 | a0001c0001t0002g0034 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.337-2096A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812454 | ||||||
| chr7:152812537
|
G | GT | 28 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(25): Show | 28 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.337-2004dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812537 | |||||
| chr7:152812566
|
A | G | 17 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(14): Show | 17 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.337-1984A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812566 | ||||||
| chr7:152812602
|
T | C | 1 | a0001c0001t0002g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.337-1948T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812602 | ||||||
| chr7:152812611
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.337-1939G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812611 | ||||||
| chr7:152812843
|
G | A | 120 | a0001c0001t0001g0182a0001c0001t0001g0200a0001c0001t0001g0213others(117): Show | 120 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.337-1707G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812843 | ||||||
| chr7:152812874
|
G | T | 247 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.337-1676G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812874 | ||||||
| chr7:152812899
|
TC | T | 155 | a0001c0001t0001g0003a0001c0001t0001g0184a0001c0001t0001g0186others(152): Show | 156 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.337-1650delC | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812899 | ||||||
| chr7:152813406
|
G | A | 1 | a0001c0001t0002g0027 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.337-1144G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152813406 | ||||||
| chr7:152813420
|
T | C | 1 | a0001c0001t0002g0027 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.337-1130T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152813420 | ||||||
| chr7:152813421
|
G | C | 1 | a0001c0001t0002g0027 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.337-1129G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152813421 | ||||||
| chr7:152813435
|
C | T | 1 | a0001c0001t0002g0027 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.337-1115C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152813435 | ||||||
| chr7:152813438
|
T | C | 117 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(114): Show | 117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.337-1112T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152813438 | ||||||
| chr7:152813455
|
A | G | 38 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(35): Show | 38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.337-1095A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152813455 | ||||||
| chr7:152813493
|
C | G | 1 | a0001c0001t0002g0027 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.337-1057C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152813493 | ||||||
| chr7:152813516
|
A | G | 5 | a0001c0001t0002g0007a0001c0001t0002g0155a0001c0001t0002g0156others(2): Show | 5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.337-1034A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152813516 | ||||||
| chr7:152813529
|
TA | T | 117 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(114): Show | 117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.337-1020delA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152813529 | ||||||
| chr7:152813613
|
C | T | 1 | a0001c0001t0002g0027 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.337-937C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152813613 | ||||||
| chr7:152813667
|
A | G | 1 | a0001c0001t0002g0103 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.337-883A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152813667 | ||||||
| chr7:152813670
|
G | A | 1 | a0001c0001t0002g0089 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.337-880G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152813670 | ||||||
| chr7:152813831
|
G | A | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.337-719G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152813831 | ||||||
| chr7:152813865
|
CTTTTCTC others(2): Show |
C | 13 | a0001c0001t0001g0296a0001c0001t0002g0002a0001c0001t0002g0007others(10): Show | 14 | HG01074.hp2 HG01099.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.337-683_337-675del others(9): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152813865 | |||||
| chr7:152813939
|
C | T | 6 | a0001c0001t0001g0200a0001c0001t0002g0068a0001c0001t0002g0069others(3): Show | 6 | HG00099.hp1 HG00738.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.337-611C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152813939 | ||||||
| chr7:152814042
|
C | G | 2 | a0001c0001t0002g0057a0001c0001t0002g0091 | 2 | NA18957.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.337-508C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152814042 | ||||||
| chr7:152814111
|
C | T | 1 | a0001c0001t0002g0055 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.337-439C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152814111 | ||||||
| chr7:152814202
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.337-348G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152814202 | ||||||
| chr7:152814206
|
T | G | 24 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(21): Show | 24 | HG01074.hp2 HG01099.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.337-344T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152814206 | ||||||
| chr7:152814257
|
G | A | 119 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(116): Show | 119 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.337-293G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152814257 | ||||||
| chr7:152814274
|
C | T | 1 | a0001c0001t0002g0027 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.337-276C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152814274 | ||||||
| chr7:152814389
|
T | C | 292 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(289): Show | 295 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(292): Show |
intron_variant | MODIFIER | c.337-161T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152814389 | ||||||
| chr7:152814513
|
C | T | 254 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.337-37C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152814513 | ||||||
| chr7:152814531
|
A | G | 8 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0028others(5): Show | 8 | HG02055.hp1 HG02572.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.337-19A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152814531 | ||||||
| chr7:152814696
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.432+51C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152814696 | ||||||
| chr7:152814772
|
C | T | 11 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(8): Show | 11 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.432+127C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152814772 | ||||||
| chr7:152814976
|
C | T | 5 | a0001c0001t0002g0007a0001c0001t0002g0155a0001c0001t0002g0156others(2): Show | 5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.432+331C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152814976 | ||||||
| chr7:152815208
|
A | G | 1 | a0001c0001t0001g0277 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.432+563A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152815208 | ||||||
| chr7:152815295
|
C | T | 5 | a0001c0001t0002g0007a0001c0001t0002g0155a0001c0001t0002g0156others(2): Show | 5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.432+650C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152815295 | ||||||
| chr7:152815310
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.432+665C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152815310 | ||||||
| chr7:152815363
|
T | C | 57 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(54): Show | 57 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.432+718T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152815363 | ||||||
| chr7:152815373
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.432+728C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152815373 | ||||||
| chr7:152815468
|
G | A | 243 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(240): Show | 245 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.432+823G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152815468 | ||||||
| chr7:152815544
|
G | A | 118 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(115): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.432+899G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152815544 | ||||||
| chr7:152815571
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.433-910G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152815571 | ||||||
| chr7:152815621
|
G | A | 74 | a0001c0001t0001g0003a0001c0001t0001g0201a0001c0001t0001g0202others(71): Show | 75 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.433-860G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152815621 | ||||||
| chr7:152815666
|
G | A | 21 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(18): Show | 21 | HG01099.hp2 HG01106.hp2 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.433-815G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152815666 | ||||||
| chr7:152815951
|
C | T | 245 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(242): Show | 246 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(243): Show |
intron_variant | MODIFIER | c.433-530C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152815951 | ||||||
| chr7:152815979
|
C | T | 2 | a0001c0001t0001g0299a0001c0001t0001g0304 | 2 | HG01952.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.433-502C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152815979 | ||||||
| chr7:152816032
|
G | A | 13 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0298others(10): Show | 13 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.433-449G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152816032 | ||||||
| chr7:152816089
|
C | T | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.433-392C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152816089 | ||||||
| chr7:152816169
|
A | G | 2 | a0001c0001t0001g0207a0001c0001t0001g0247 | 2 | HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.433-312A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152816169 | ||||||
| chr7:152816284
|
A | C | 17 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(14): Show | 17 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.433-197A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152816284 | ||||||
| chr7:152816384
|
T | C | 1 | a0001c0001t0002g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.433-97T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152816384 | ||||||
| chr7:152816455
|
G | A | 5 | a0001c0001t0002g0007a0001c0001t0002g0155a0001c0001t0002g0156others(2): Show | 5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.433-26G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152816455 | ||||||
| chr7:152816477
|
C | G | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | splice_region_variant&intron_variant | LOW | c.433-4C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152816477 | ||||||
| chr7:152816638
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.540+50C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152816638 | ||||||
| chr7:152816655
|
T | TA | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(5): Show | 8 | HG00609.hp1 HG01099.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.540+81dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | 152816655 | |||||
| chr7:152816684
|
G | A | 156 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(153): Show | 156 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.540+96G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152816684 | ||||||
| chr7:152816754
|
A | G | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.540+166A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152816754 | ||||||
| chr7:152816769
|
G | T | 19 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(16): Show | 19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.540+181G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152816769 | ||||||
| chr7:152816780
|
A | C | 1 | a0001c0001t0001g0118 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.540+192A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152816780 | ||||||
| chr7:152816846
|
A | G | 2 | a0001c0001t0001g0298a0001c0001t0001g0300 | 2 | HG02145.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.540+258A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152816846 | ||||||
| chr7:152816874
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG01099.hp2 HG01106.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.540+286G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152816874 | ||||||
| chr7:152816907
|
C | T | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0242others(1): Show | 4 | HG00735.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+319C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152816907 | ||||||
| chr7:152816908
|
G | A | 95 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0225others(92): Show | 95 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.540+320G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152816908 | ||||||
| chr7:152816910
|
G | A | 15 | a0001c0001t0001g0003a0001c0001t0001g0236a0001c0001t0001g0237others(12): Show | 16 | HG00735.hp1 HG01109.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.540+322G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152816910 | ||||||
| chr7:152816937
|
T | C | 150 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(147): Show | 150 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.540+349T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152816937 | ||||||
| chr7:152816970
|
C | T | 1 | a0001c0001t0002g0082 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.540+382C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152816970 | ||||||
| chr7:152817074
|
T | C | 6 | a0001c0001t0001g0302a0001c0001t0002g0157a0001c0001t0002g0158others(3): Show | 6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+486T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152817074 | ||||||
| chr7:152817112
|
C | T | 11 | a0001c0001t0003g0166a0001c0001t0003g0168a0001c0001t0003g0173others(8): Show | 11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.540+524C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152817112 | ||||||
| chr7:152817122
|
C | T | 2 | a0001c0001t0001g0299a0001c0001t0001g0304 | 2 | HG01952.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.540+534C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152817122 | ||||||
| chr7:152817295
|
C | T | 1 | a0001c0001t0001g0182 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.540+707C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152817295 | ||||||
| chr7:152817575
|
G | A | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0242others(1): Show | 4 | HG00735.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+987G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152817575 | ||||||
| chr7:152817610
|
T | G | 160 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(157): Show | 160 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.540+1022T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152817610 | ||||||
| chr7:152817638
|
TCTC | T | 4 | a0001c0001t0001g0217a0001c0001t0001g0222a0001c0001t0001g0223others(1): Show | 4 | NA18951.hp1 NA19007.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+1057_540+1059d others(5): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | 152817638 | |||||
| chr7:152817714
|
G | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.540+1126G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152817714 | ||||||
| chr7:152817984
|
G | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.540+1396G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152817984 | ||||||
| chr7:152818172
|
G | A | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.540+1584G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152818172 | ||||||
| chr7:152818254
|
CA | C | 13 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0298others(10): Show | 13 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.540+1667delA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152818254 | ||||||
| chr7:152818330
|
G | A | 2 | a0001c0001t0001g0299a0001c0001t0001g0304 | 2 | HG01952.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.540+1742G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152818330 | ||||||
| chr7:152818341
|
A | G | 9 | a0001c0001t0001g0003a0001c0001t0001g0288a0001c0001t0001g0289others(6): Show | 10 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.540+1753A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152818341 | ||||||
| chr7:152818409
|
A | G | 1 | a0001c0001t0001g0269 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.540+1821A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152818409 | ||||||
| chr7:152818456
|
CT | C | 155 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(152): Show | 155 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.541-1833delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | 152818456 | |||||
| chr7:152818533
|
C | G | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.541-1766C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152818533 | ||||||
| chr7:152818547
|
T | G | 5 | a0001c0001t0001g0187a0001c0001t0001g0190a0001c0001t0001g0191others(2): Show | 5 | NA18942.hp1 NA18955.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.541-1752T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152818547 | ||||||
| chr7:152818568
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.541-1731G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152818568 | ||||||
| chr7:152818777
|
C | T | 9 | a0001c0001t0001g0003a0001c0001t0001g0288a0001c0001t0001g0289others(6): Show | 10 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.541-1522C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152818777 | ||||||
| chr7:152818876
|
G | A | 117 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(114): Show | 117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.541-1423G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152818876 | ||||||
| chr7:152819022
|
A | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.541-1277A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152819022 | ||||||
| chr7:152819279
|
G | A | 155 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(152): Show | 155 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.541-1020G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152819279 | ||||||
| chr7:152819320
|
C | T | 29 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204others(26): Show | 29 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.541-979C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152819320 | ||||||
| chr7:152819386
|
C | T | 1 | a0001c0001t0002g0032 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.541-913C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152819386 | ||||||
| chr7:152819474
|
A | G | 1 | a0001c0005t0001g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.541-825A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152819474 | ||||||
| chr7:152819523
|
C | T | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0242others(1): Show | 4 | HG00735.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.541-776C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152819523 | ||||||
| chr7:152819610
|
G | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.541-689G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152819610 | ||||||
| chr7:152819894
|
G | A | 2 | a0001c0001t0001g0233a0001c0001t0001g0274 | 2 | HG00609.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.541-405G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152819894 | ||||||
| chr7:152819987
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.541-312C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152819987 | ||||||
| chr7:152820132
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.541-167T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152820132 | ||||||
| chr7:152820170
|
G | T | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.541-129G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152820170 | ||||||
| chr7:152820256
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.541-43C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152820256 | ||||||
| chr7:152820639
|
T | C | 156 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(153): Show | 156 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.684+197T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152820639 | ||||||
| chr7:152820769
|
C | T | 5 | a0001c0001t0002g0007a0001c0001t0002g0155a0001c0001t0002g0156others(2): Show | 5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.684+327C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152820769 | ||||||
| chr7:152820792
|
A | G | 1 | a0001c0001t0001g0297 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.684+350A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152820792 | ||||||
| chr7:152820809
|
C | T | 74 | a0001c0001t0001g0003a0001c0001t0001g0201a0001c0001t0001g0202others(71): Show | 75 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.684+367C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152820809 | ||||||
| chr7:152820897
|
C | T | 11 | a0001c0001t0003g0166a0001c0001t0003g0168a0001c0001t0003g0173others(8): Show | 11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.684+455C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152820897 | ||||||
| chr7:152820978
|
C | T | 5 | a0001c0001t0002g0007a0001c0001t0002g0155a0001c0001t0002g0156others(2): Show | 5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.684+536C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152820978 | ||||||
| chr7:152821075
|
T | A | 19 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(16): Show | 19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.684+633T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152821075 | ||||||
| chr7:152821079
|
G | A | 9 | a0001c0001t0001g0003a0001c0001t0001g0288a0001c0001t0001g0289others(6): Show | 10 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.684+637G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152821079 | ||||||
| chr7:152821135
|
C | T | 74 | a0001c0001t0001g0003a0001c0001t0001g0201a0001c0001t0001g0202others(71): Show | 75 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.684+693C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152821135 | ||||||
| chr7:152821161
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(1): Show | 5 | HG01109.hp2 HG01243.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.684+719G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152821161 | ||||||
| chr7:152821199
|
T | A | 17 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(14): Show | 17 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.684+757T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152821199 | ||||||
| chr7:152821309
|
C | T | 1 | a0001c0001t0009g0142 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.684+867C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152821309 | ||||||
| chr7:152821332
|
A | T | 19 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(16): Show | 19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.684+890A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152821332 | ||||||
| chr7:152821472
|
G | GA | 24 | a0001c0001t0001g0113a0001c0001t0001g0184a0001c0001t0001g0186others(21): Show | 24 | HG00735.hp1 HG01109.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.684+1043dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr7 | 152821472 | |||||
| chr7:152821532
|
C | G | 1 | a0001c0001t0001g0236 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.684+1090C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152821532 | ||||||
| chr7:152821567
|
A | G | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.684+1125A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152821567 | ||||||
| chr7:152821641
|
A | G | 72 | a0001c0001t0001g0003a0001c0001t0001g0201a0001c0001t0001g0202others(69): Show | 73 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.684+1199A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152821641 | ||||||
| chr7:152821840
|
C | A | 1 | a0001c0001t0001g0115 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.684+1398C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152821840 | ||||||
| chr7:152821872
|
T | C | 254 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.684+1430T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152821872 | ||||||
| chr7:152821992
|
A | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.685-1350A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152821992 | ||||||
| chr7:152822083
|
G | A | 1 | a0001c0001t0001g0298 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.685-1259G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152822083 | ||||||
| chr7:152822171
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.685-1171C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152822171 | ||||||
| chr7:152822306
|
C | T | 136 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(133): Show | 136 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.685-1036C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152822306 | ||||||
| chr7:152822328
|
G | A | 19 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(16): Show | 19 | HG01099.hp2 HG01106.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.685-1014G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152822328 | ||||||
| chr7:152822363
|
C | T | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.685-979C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152822363 | ||||||
| chr7:152822460
|
C | T | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0242others(1): Show | 4 | HG00735.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.685-882C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152822460 | ||||||
| chr7:152822556
|
C | T | 19 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(16): Show | 19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.685-786C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152822556 | ||||||
| chr7:152822677
|
C | T | 19 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(16): Show | 19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.685-665C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152822677 | ||||||
| chr7:152822955
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.685-387C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152822955 | ||||||
| chr7:152822956
|
G | T | 2 | a0001c0001t0001g0186a0001c0001t0001g0193 | 2 | NA18939.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.685-386G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152822956 | ||||||
| chr7:152823001
|
C | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0269a0001c0001t0001g0288others(7): Show | 11 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.685-341C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152823001 | ||||||
| chr7:152823028
|
G | C | 19 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(16): Show | 19 | HG01099.hp2 HG01106.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.685-314G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152823028 | ||||||
| chr7:152823080
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.685-262C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152823080 | ||||||
| chr7:152823181
|
A | T | 6 | a0001c0001t0001g0302a0001c0001t0002g0157a0001c0001t0002g0158others(3): Show | 6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.685-161A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152823181 | ||||||
| chr7:152823190
|
T | C | 19 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(16): Show | 19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.685-152T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152823190 | ||||||
| chr7:152823221
|
T | TA | 21 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(18): Show | 21 | HG01074.hp2 HG01109.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.685-120dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr7 | 152823221 | |||||
| chr7:152823303
|
G | A | 6 | a0001c0001t0001g0224a0001c0001t0001g0232a0001c0001t0001g0233others(3): Show | 6 | HG00597.hp2 HG00609.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.685-39G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152823303 | ||||||
| chr7:152823621
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.858+106C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 8/11 | chr7 | 152823621 | ||||||
| chr7:152823646
|
T | C | 158 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(155): Show | 158 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.858+131T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 8/11 | chr7 | 152823646 | ||||||
| chr7:152823650
|
C | T | 6 | a0001c0001t0001g0302a0001c0001t0002g0157a0001c0001t0002g0158others(3): Show | 6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.858+135C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 8/11 | chr7 | 152823650 | ||||||
| chr7:152823757
|
A | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.858+242A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 8/11 | chr7 | 152823757 | ||||||
| chr7:152823803
|
GT | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.858+289delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 8/11 | chr7 | 152823803 | ||||||
| chr7:152823855
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.858+340C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 8/11 | chr7 | 152823855 | ||||||
| chr7:152823899
|
G | A | 3 | a0001c0001t0001g0289a0001c0001t0001g0293a0001c0001t0005g0290 | 3 | HG02809.hp2 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.858+384G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 8/11 | chr7 | 152823899 | ||||||
| chr7:152823950
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.858+435A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 8/11 | chr7 | 152823950 | ||||||
| chr7:152824412
|
A | G | 21 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(18): Show | 21 | HG01074.hp2 HG01109.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.859-618A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 8/11 | chr7 | 152824412 | ||||||
| chr7:152824418
|
A | G | 1 | a0001c0001t0001g0120 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.859-612A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 8/11 | chr7 | 152824418 | ||||||
| chr7:152824864
|
G | A | 6 | a0001c0001t0001g0302a0001c0001t0002g0157a0001c0001t0002g0158others(3): Show | 6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.859-166G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 8/11 | chr7 | 152824864 | ||||||
| chr7:152824868
|
T | A | 254 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.859-162T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 8/11 | chr7 | 152824868 | ||||||
| chr7:152825304
|
T | TTTTTA | 74 | a0001c0001t0001g0003a0001c0001t0001g0201a0001c0001t0001g0202others(71): Show | 75 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.951+202_951+206dup others(5): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152825304 | |||||
| chr7:152825335
|
G | A | 6 | a0001c0001t0001g0302a0001c0001t0002g0157a0001c0001t0002g0158others(3): Show | 6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.951+213G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152825335 | ||||||
| chr7:152825354
|
C | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.951+232C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152825354 | ||||||
| chr7:152825505
|
C | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.951+383C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152825505 | ||||||
| chr7:152825538
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.951+416A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152825538 | ||||||
| chr7:152825759
|
C | T | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(3): Show | 6 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.951+637C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152825759 | ||||||
| chr7:152825816
|
C | T | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.951+694C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152825816 | ||||||
| chr7:152825881
|
A | T | 1 | a0001c0001t0002g0101 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.951+759A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152825881 | ||||||
| chr7:152826026
|
A | T | 1 | a0001c0001t0001g0287 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.951+904A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152826026 | ||||||
| chr7:152826064
|
G | T | 8 | a0001c0001t0003g0166a0001c0001t0003g0168a0001c0001t0003g0173others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.951+942G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152826064 | ||||||
| chr7:152826149
|
G | A | 19 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(16): Show | 19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.951+1027G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152826149 | ||||||
| chr7:152826197
|
T | C | 3 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0018 | 3 | NA18989.hp2 NA19002.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.951+1075T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152826197 | ||||||
| chr7:152826360
|
CTT | C | 8 | a0001c0001t0001g0296a0001c0001t0002g0002a0001c0001t0002g0019others(5): Show | 9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.951+1241_951+1242d others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152826360 | |||||
| chr7:152826481
|
T | C | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.951+1359T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152826481 | ||||||
| chr7:152826555
|
T | C | 1 | a0001c0001t0002g0045 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.951+1433T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152826555 | ||||||
| chr7:152826928
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+1806C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152826928 | ||||||
| chr7:152827012
|
C | G | 96 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0225others(93): Show | 96 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.951+1890C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827012 | ||||||
| chr7:152827043
|
G | A | 7 | a0001c0001t0001g0131a0001c0001t0001g0302a0001c0001t0002g0157others(4): Show | 7 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.951+1921G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827043 | ||||||
| chr7:152827063
|
C | A | 6 | a0001c0001t0001g0302a0001c0001t0002g0157a0001c0001t0002g0158others(3): Show | 6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.951+1941C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827063 | ||||||
| chr7:152827063
|
C | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.951+1941C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827063 | ||||||
| chr7:152827107
|
A | G | 1 | a0001c0001t0002g0024 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.951+1985A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827107 | ||||||
| chr7:152827108
|
A | G | 19 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(16): Show | 19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.951+1986A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827108 | ||||||
| chr7:152827282
|
G | A | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+2160G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827282 | ||||||
| chr7:152827288
|
G | A | 11 | a0001c0001t0003g0166a0001c0001t0003g0168a0001c0001t0003g0173others(8): Show | 11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.951+2166G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827288 | ||||||
| chr7:152827307
|
C | T | 1 | a0001c0001t0002g0072 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.951+2185C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827307 | ||||||
| chr7:152827415
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.951+2293T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827415 | ||||||
| chr7:152827486
|
T | G | 1 | a0001c0001t0001g0293 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.951+2364T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827486 | ||||||
| chr7:152827503
|
T | C | 19 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(16): Show | 19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.951+2381T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827503 | ||||||
| chr7:152827533
|
C | T | 38 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(35): Show | 38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.951+2411C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827533 | ||||||
| chr7:152827544
|
G | T | 1 | a0001c0001t0001g0154 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.951+2422G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827544 | ||||||
| chr7:152827699
|
C | T | 19 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(16): Show | 19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.951+2577C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827699 | ||||||
| chr7:152827855
|
C | T | 1 | a0001c0001t0002g0156 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.951+2733C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827855 | ||||||
| chr7:152827896
|
GT | G | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+2782delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152827896 | |||||
| chr7:152827958
|
A | T | 5 | a0001c0001t0002g0157a0001c0001t0002g0158a0001c0001t0002g0163others(2): Show | 5 | HG03490.hp1 HG03491.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+2836A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827958 | ||||||
| chr7:152828160
|
T | C | 93 | a0001c0001t0001g0003a0001c0001t0001g0184a0001c0001t0001g0186others(90): Show | 94 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.951+3038T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828160 | ||||||
| chr7:152828184
|
T | C | 1 | a0001c0001t0008g0307 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.951+3062T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828184 | ||||||
| chr7:152828197
|
T | C | 1 | a0001c0001t0001g0229 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.951+3075T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828197 | ||||||
| chr7:152828206
|
G | A | 1 | a0001c0001t0002g0096 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.951+3084G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828206 | ||||||
| chr7:152828276
|
C | A | 19 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(16): Show | 19 | HG01099.hp2 HG01106.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.951+3154C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828276 | ||||||
| chr7:152828344
|
C | T | 117 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(114): Show | 117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.951+3222C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828344 | ||||||
| chr7:152828353
|
T | G | 59 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(56): Show | 59 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.951+3231T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828353 | ||||||
| chr7:152828360
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.951+3238T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828360 | ||||||
| chr7:152828367
|
T | C | 1 | a0001c0001t0002g0086 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.951+3245T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828367 | ||||||
| chr7:152828451
|
G | T | 13 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0298others(10): Show | 13 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.951+3329G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828451 | ||||||
| chr7:152828518
|
G | A | 1 | a0001c0001t0009g0142 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.951+3396G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828518 | ||||||
| chr7:152828580
|
C | T | 1 | a0001c0001t0001g0219 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.951+3458C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828580 | ||||||
| chr7:152828643
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.951+3521C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828643 | ||||||
| chr7:152828644
|
G | A | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+3522G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828644 | ||||||
| chr7:152828674
|
C | A | 1 | a0001c0001t0001g0146 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.951+3552C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828674 | ||||||
| chr7:152828688
|
T | A | 1 | a0001c0001t0001g0305 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.951+3566T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828688 | ||||||
| chr7:152828737
|
G | C | 1 | a0001c0001t0001g0300 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.951+3615G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828737 | ||||||
| chr7:152828772
|
C | A | 2 | a0001c0001t0002g0045a0001c0001t0002g0092 | 2 | HG02165.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.951+3650C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828772 | ||||||
| chr7:152828811
|
A | G | 118 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(115): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.951+3689A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828811 | ||||||
| chr7:152828975
|
T | G | 1 | a0001c0001t0002g0178 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.951+3853T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828975 | ||||||
| chr7:152829032
|
T | A | 13 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0298others(10): Show | 13 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.951+3910T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152829032 | ||||||
| chr7:152829034
|
G | T | 13 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0298others(10): Show | 13 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.951+3912G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152829034 | ||||||
| chr7:152829035
|
T | G | 13 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0298others(10): Show | 13 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.951+3913T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152829035 | ||||||
| chr7:152829036
|
G | A | 13 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0298others(10): Show | 13 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.951+3914G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152829036 | ||||||
| chr7:152829040
|
GTGTGTAT others(19): Show |
G | 13 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0298others(10): Show | 13 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.951+3919_951+3944d others(28): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152829040 | ||||||
| chr7:152829044
|
G | GTGTA | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+3923_951+3924i others(6): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152829044 | |||||
| chr7:152829055
|
T | C | 1 | a0001c0001t0001g0220 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.951+3933T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152829055 | ||||||
| chr7:152829057
|
T | C | 79 | a0001c0001t0001g0003a0001c0001t0001g0201a0001c0001t0001g0202others(76): Show | 80 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.951+3935T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152829057 | ||||||
| chr7:152829057
|
T | TATATATA others(3): Show |
1 | a0001c0001t0001g0192 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.951+3936_951+3937i others(12): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152829057 | |||||
| chr7:152829057
|
T | TATATATA others(3): Show |
14 | a0001c0001t0001g0184a0001c0001t0001g0187a0001c0001t0001g0188others(11): Show | 14 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.951+3936_951+3937i others(12): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152829057 | |||||
| chr7:152829057
|
T | TATATATA others(5): Show |
1 | a0001c0001t0001g0199 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.951+3936_951+3937i others(14): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152829057 | |||||
| chr7:152829059
|
C | T | 2 | a0001c0001t0005g0183a0001c0001t0008g0307 | 2 | HG02723.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.951+3937C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152829059 | ||||||
| chr7:152829061
|
C | T | 1 | a0001c0001t0008g0307 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.951+3939C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152829061 | ||||||
| chr7:152829546
|
A | G | 1 | a0001c0001t0008g0307 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.951+4424A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152829546 | ||||||
| chr7:152829839
|
G | A | 38 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(35): Show | 38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.951+4717G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152829839 | ||||||
| chr7:152829873
|
C | G | 74 | a0001c0001t0001g0003a0001c0001t0001g0201a0001c0001t0001g0202others(71): Show | 75 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.951+4751C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152829873 | ||||||
| chr7:152830041
|
A | C | 1 | a0001c0001t0001g0118 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.951+4919A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152830041 | ||||||
| chr7:152830462
|
G | T | 8 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(5): Show | 8 | HG02486.hp1 HG02717.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.951+5340G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152830462 | ||||||
| chr7:152830583
|
CTG | C | 11 | a0001c0001t0003g0166a0001c0001t0003g0168a0001c0001t0003g0173others(8): Show | 11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.951+5463_951+5464d others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152830583 | |||||
| chr7:152830675
|
A | G | 2 | a0001c0001t0001g0207a0001c0001t0001g0247 | 2 | HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.951+5553A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152830675 | ||||||
| chr7:152830758
|
T | C | 254 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.951+5636T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152830758 | ||||||
| chr7:152830893
|
T | C | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+5771T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152830893 | ||||||
| chr7:152831022
|
G | T | 1 | a0001c0001t0002g0051 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.951+5900G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152831022 | ||||||
| chr7:152831144
|
A | T | 1 | a0001c0001t0001g0265 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.951+6022A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152831144 | ||||||
| chr7:152831175
|
T | C | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+6053T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152831175 | ||||||
| chr7:152831257
|
G | A | 8 | a0001c0001t0001g0296a0001c0001t0002g0002a0001c0001t0002g0019others(5): Show | 9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.951+6135G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152831257 | ||||||
| chr7:152831288
|
A | G | 11 | a0001c0001t0003g0166a0001c0001t0003g0168a0001c0001t0003g0173others(8): Show | 11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.951+6166A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152831288 | ||||||
| chr7:152831313
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.951+6191C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152831313 | ||||||
| chr7:152831336
|
G | C | 1 | a0001c0001t0002g0051 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.951+6214G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152831336 | ||||||
| chr7:152831359
|
AGGGCTGT others(3): Show |
A | 9 | a0001c0001t0001g0201a0001c0001t0001g0272a0001c0001t0001g0273others(6): Show | 9 | HG02258.hp2 HG02486.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.951+6241_951+6250d others(12): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152831359 | |||||
| chr7:152831451
|
G | A | 2 | a0001c0001t0001g0229a0001c0001t0001g0234 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.951+6329G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152831451 | ||||||
| chr7:152831466
|
G | A | 2 | a0001c0001t0002g0104a0001c0001t0002g0105 | 2 | HG02055.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.951+6344G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152831466 | ||||||
| chr7:152831605
|
G | A | 19 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(16): Show | 19 | HG01099.hp2 HG01106.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.951+6483G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152831605 | ||||||
| chr7:152831618
|
C | T | 11 | a0001c0001t0003g0166a0001c0001t0003g0168a0001c0001t0003g0173others(8): Show | 11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.951+6496C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152831618 | ||||||
| chr7:152831810
|
C | T | 38 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(35): Show | 38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.951+6688C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152831810 | ||||||
| chr7:152831890
|
G | A | 117 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(114): Show | 117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.951+6768G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152831890 | ||||||
| chr7:152832056
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.951+6934A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832056 | ||||||
| chr7:152832094
|
A | G | 38 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(35): Show | 38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.951+6972A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832094 | ||||||
| chr7:152832140
|
C | G | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.951+7018C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832140 | ||||||
| chr7:152832147
|
A | C | 1 | a0001c0001t0002g0051 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.951+7025A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832147 | ||||||
| chr7:152832403
|
A | G | 1 | a0001c0001t0002g0042 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.951+7281A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832403 | ||||||
| chr7:152832429
|
C | T | 3 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0176 | 3 | HG01891.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.951+7307C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832429 | ||||||
| chr7:152832479
|
G | A | 6 | a0001c0001t0001g0302a0001c0001t0002g0157a0001c0001t0002g0158others(3): Show | 6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.951+7357G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832479 | ||||||
| chr7:152832530
|
T | C | 1 | a0001c0001t0002g0031 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.951+7408T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832530 | ||||||
| chr7:152832612
|
C | T | 2 | a0001c0001t0002g0045a0001c0001t0002g0092 | 2 | HG02165.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.951+7490C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832612 | ||||||
| chr7:152832778
|
C | G | 1 | a0001c0001t0002g0051 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.951+7656C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832778 | ||||||
| chr7:152832778
|
C | T | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+7656C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832778 | ||||||
| chr7:152832779
|
G | C | 1 | a0001c0001t0002g0051 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.951+7657G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832779 | ||||||
| chr7:152832793
|
C | T | 118 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(115): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.951+7671C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832793 | ||||||
| chr7:152832901
|
A | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+7779A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832901 | ||||||
| chr7:152832921
|
T | C | 43 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(40): Show | 43 | HG00735.hp1 HG01099.hp2 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.951+7799T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832921 | ||||||
| chr7:152832987
|
C | T | 1 | a0001c0001t0002g0042 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.951+7865C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832987 | ||||||
| chr7:152833053
|
A | G | 1 | a0001c0001t0002g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.951+7931A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833053 | ||||||
| chr7:152833173
|
G | A | 8 | a0001c0001t0001g0296a0001c0001t0002g0002a0001c0001t0002g0019others(5): Show | 9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.951+8051G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833173 | ||||||
| chr7:152833231
|
A | G | 8 | a0001c0001t0001g0296a0001c0001t0002g0002a0001c0001t0002g0019others(5): Show | 9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.951+8109A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833231 | ||||||
| chr7:152833261
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.951+8139G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833261 | ||||||
| chr7:152833262
|
C | A | 1 | a0001c0001t0002g0071 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.951+8140C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833262 | ||||||
| chr7:152833264
|
G | A | 1 | a0001c0001t0002g0010 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.951+8142G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833264 | ||||||
| chr7:152833268
|
A | T | 1 | a0001c0001t0002g0071 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.951+8146A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833268 | ||||||
| chr7:152833406
|
A | G | 118 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(115): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.951+8284A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833406 | ||||||
| chr7:152833496
|
T | A | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+8374T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833496 | ||||||
| chr7:152833527
|
G | A | 12 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0242others(9): Show | 12 | HG00735.hp1 HG02451.hp1 HG02976.hp1 others(9): Show |
intron_variant | MODIFIER | c.951+8405G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833527 | ||||||
| chr7:152833533
|
G | A | 6 | a0001c0001t0002g0051a0001c0001t0002g0157a0001c0001t0002g0158others(3): Show | 6 | HG03490.hp1 HG03491.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.951+8411G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833533 | ||||||
| chr7:152833572
|
T | C | 3 | a0001c0001t0001g0289a0001c0001t0001g0293a0001c0001t0005g0290 | 3 | HG02809.hp2 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.951+8450T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833572 | ||||||
| chr7:152833610
|
TAAG | T | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+8493_951+8495d others(5): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152833610 | |||||
| chr7:152833737
|
T | C | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+8615T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833737 | ||||||
| chr7:152833789
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+8667C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833789 | ||||||
| chr7:152833800
|
C | G | 1 | a0001c0001t0002g0055 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.951+8678C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833800 | ||||||
| chr7:152833930
|
T | C | 2 | a0001c0001t0002g0171a0001c0001t0002g0172 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.951+8808T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833930 | ||||||
| chr7:152833936
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.951+8814G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833936 | ||||||
| chr7:152834092
|
T | G | 19 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(16): Show | 19 | HG01099.hp2 HG01106.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.951+8970T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152834092 | ||||||
| chr7:152834093
|
TTCTAAAT others(4): Show |
T | 19 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(16): Show | 19 | HG01099.hp2 HG01106.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.951+8972_951+8982d others(13): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152834093 | ||||||
| chr7:152834146
|
G | A | 3 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0076 | 3 | HG00544.hp1 HG00741.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.951+9024G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152834146 | ||||||
| chr7:152834155
|
G | GT | 16 | a0001c0001t0001g0122a0001c0001t0001g0147a0001c0001t0001g0181others(13): Show | 16 | HG00438.hp1 HG00609.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.951+9047dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152834155 | |||||
| chr7:152834155
|
G | T | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.951+9033G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152834155 | ||||||
| chr7:152834302
|
C | T | 5 | a0001c0001t0002g0007a0001c0001t0002g0155a0001c0001t0002g0156others(2): Show | 5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+9180C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152834302 | ||||||
| chr7:152834406
|
G | A | 3 | a0001c0001t0002g0056a0001c0001t0002g0090a0001c0001t0002g0098 | 3 | HG00438.hp1 HG02071.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.951+9284G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152834406 | ||||||
| chr7:152834443
|
C | G | 118 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(115): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.951+9321C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152834443 | ||||||
| chr7:152834446
|
G | T | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0242others(1): Show | 4 | HG00735.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.951+9324G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152834446 | ||||||
| chr7:152834563
|
C | T | 3 | a0001c0001t0001g0230a0001c0001t0001g0243a0001c0001t0001g0244 | 3 | HG02630.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.951+9441C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152834563 | ||||||
| chr7:152834627
|
C | T | 1 | a0001c0001t0002g0051 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.951+9505C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152834627 | ||||||
| chr7:152834628
|
T | C | 1 | a0001c0001t0002g0051 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.951+9506T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152834628 | ||||||
| chr7:152834680
|
G | A | 6 | a0001c0001t0001g0302a0001c0001t0002g0157a0001c0001t0002g0158others(3): Show | 6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.951+9558G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152834680 | ||||||
| chr7:152834880
|
T | G | 1 | a0001c0001t0002g0070 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.951+9758T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152834880 | ||||||
| chr7:152834946
|
A | G | 5 | a0001c0001t0002g0007a0001c0001t0002g0155a0001c0001t0002g0156others(2): Show | 5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+9824A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152834946 | ||||||
| chr7:152835055
|
G | GT | 9 | a0001c0001t0001g0296a0001c0001t0002g0002a0001c0001t0002g0019others(6): Show | 10 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.951+9944dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152835055 | |||||
| chr7:152835055
|
GT | G | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(3): Show | 6 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.951+9944delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152835055 | |||||
| chr7:152835084
|
A | C | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+9962A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152835084 | ||||||
| chr7:152835201
|
C | G | 1 | a0001c0001t0001g0221 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.951+10079C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152835201 | ||||||
| chr7:152835311
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.951+10189G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152835311 | ||||||
| chr7:152835398
|
A | C | 1 | a0001c0001t0002g0046 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.951+10276A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152835398 | ||||||
| chr7:152835531
|
T | G | 2 | a0001c0001t0001g0126a0001c0001t0001g0128 | 2 | HG00597.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.951+10409T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152835531 | ||||||
| chr7:152835671
|
G | A | 1 | a0001c0001t0002g0163 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.951+10549G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152835671 | ||||||
| chr7:152835709
|
T | G | 1 | a0001c0001t0001g0265 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.951+10587T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152835709 | ||||||
| chr7:152835834
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.951+10712C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152835834 | ||||||
| chr7:152835956
|
G | T | 254 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.951+10834G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152835956 | ||||||
| chr7:152835995
|
AC | A | 5 | a0001c0001t0002g0007a0001c0001t0002g0155a0001c0001t0002g0156others(2): Show | 5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+10874delC | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152835995 | ||||||
| chr7:152836043
|
T | C | 6 | a0001c0001t0002g0051a0001c0001t0002g0052a0001c0001t0002g0053others(3): Show | 6 | NA18942.hp2 NA18971.hp1 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.951+10921T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152836043 | ||||||
| chr7:152836126
|
G | A | 5 | a0001c0001t0002g0157a0001c0001t0002g0158a0001c0001t0002g0163others(2): Show | 5 | HG03490.hp1 HG03491.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+11004G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152836126 | ||||||
| chr7:152836417
|
A | T | 1 | a0001c0001t0001g0198 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.951+11295A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152836417 | ||||||
| chr7:152836429
|
T | C | 1 | a0001c0001t0001g0292 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.951+11307T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152836429 | ||||||
| chr7:152836566
|
G | A | 1 | a0001c0001t0002g0067 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.951+11444G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152836566 | ||||||
| chr7:152836609
|
G | A | 1 | a0001c0001t0002g0067 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.951+11487G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152836609 | ||||||
| chr7:152836615
|
T | C | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.951+11493T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152836615 | ||||||
| chr7:152836747
|
T | C | 2 | a0001c0001t0002g0027a0001c0001t0002g0097 | 2 | NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.951+11625T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152836747 | ||||||
| chr7:152836893
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.951+11771G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152836893 | ||||||
| chr7:152836900
|
A | T | 59 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(56): Show | 59 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.951+11778A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152836900 | ||||||
| chr7:152836927
|
T | A | 13 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0298others(10): Show | 13 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.951+11805T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152836927 | ||||||
| chr7:152837175
|
C | CA | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+12062dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152837175 | |||||
| chr7:152837181
|
A | C | 2 | a0001c0001t0001g0238a0001c0001t0001g0268 | 2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.951+12059A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152837181 | ||||||
| chr7:152837184
|
A | C | 1 | a0001c0001t0001g0184 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.951+12062A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152837184 | ||||||
| chr7:152837287
|
G | A | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+12165G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152837287 | ||||||
| chr7:152837297
|
G | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.951+12175G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152837297 | ||||||
| chr7:152837567
|
A | G | 1 | a0001c0001t0002g0101 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.951+12445A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152837567 | ||||||
| chr7:152837603
|
C | A | 1 | a0001c0001t0002g0090 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.951+12481C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152837603 | ||||||
| chr7:152837720
|
G | T | 1 | a0001c0001t0002g0046 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.951+12598G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152837720 | ||||||
| chr7:152837765
|
C | T | 8 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0302others(5): Show | 8 | HG02615.hp1 HG02630.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.951+12643C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152837765 | ||||||
| chr7:152837789
|
A | G | 19 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(16): Show | 19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.951+12667A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152837789 | ||||||
| chr7:152837837
|
A | C | 38 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(35): Show | 38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.951+12715A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152837837 | ||||||
| chr7:152837854
|
G | A | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.951+12732G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152837854 | ||||||
| chr7:152837912
|
C | G | 38 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0113others(35): Show | 39 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.951+12790C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152837912 | ||||||
| chr7:152838085
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.951+12963C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152838085 | ||||||
| chr7:152838342
|
A | G | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.951+13220A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152838342 | ||||||
| chr7:152838374
|
T | C | 2 | a0001c0001t0001g0238a0001c0001t0001g0268 | 2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.951+13252T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152838374 | ||||||
| chr7:152838384
|
A | G | 74 | a0001c0001t0001g0003a0001c0001t0001g0201a0001c0001t0001g0202others(71): Show | 75 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.951+13262A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152838384 | ||||||
| chr7:152838435
|
A | T | 1 | a0001c0003t0003g0167 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.951+13313A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152838435 | ||||||
| chr7:152838448
|
C | A | 1 | a0001c0001t0007g0059 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.951+13326C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152838448 | ||||||
| chr7:152838449
|
A | C | 1 | a0001c0001t0007g0059 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.951+13327A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152838449 | ||||||
| chr7:152838808
|
A | G | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(3): Show | 6 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.952-13318A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152838808 | ||||||
| chr7:152838811
|
C | G | 38 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(35): Show | 38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.952-13315C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152838811 | ||||||
| chr7:152838823
|
T | C | 230 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.952-13303T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152838823 | ||||||
| chr7:152838990
|
G | T | 38 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(35): Show | 38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.952-13136G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152838990 | ||||||
| chr7:152839014
|
G | T | 4 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0165others(1): Show | 4 | HG01074.hp2 HG01099.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.952-13112G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839014 | ||||||
| chr7:152839015
|
C | T | 4 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0165others(1): Show | 4 | HG01074.hp2 HG01099.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.952-13111C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839015 | ||||||
| chr7:152839029
|
C | T | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(3): Show | 6 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.952-13097C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839029 | ||||||
| chr7:152839129
|
A | T | 1 | a0001c0001t0007g0059 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.952-12997A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839129 | ||||||
| chr7:152839146
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.952-12980A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839146 | ||||||
| chr7:152839147
|
G | T | 1 | a0001c0001t0001g0108 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.952-12979G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839147 | ||||||
| chr7:152839188
|
C | T | 8 | a0001c0001t0001g0296a0001c0001t0002g0002a0001c0001t0002g0019others(5): Show | 9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.952-12938C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839188 | ||||||
| chr7:152839196
|
G | A | 1 | a0001c0001t0002g0060 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.952-12930G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839196 | ||||||
| chr7:152839236
|
C | T | 254 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.952-12890C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839236 | ||||||
| chr7:152839264
|
C | CG | 74 | a0001c0001t0001g0003a0001c0001t0001g0120a0001c0001t0001g0201others(71): Show | 75 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.952-12856dupG | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152839264 | |||||
| chr7:152839438
|
C | A | 1 | a0001c0005t0001g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.952-12688C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839438 | ||||||
| chr7:152839453
|
C | T | 19 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(16): Show | 19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.952-12673C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839453 | ||||||
| chr7:152839454
|
G | C | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.952-12672G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839454 | ||||||
| chr7:152839494
|
T | A | 38 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(35): Show | 38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.952-12632T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839494 | ||||||
| chr7:152839531
|
T | C | 59 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(56): Show | 59 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.952-12595T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839531 | ||||||
| chr7:152839648
|
C | T | 13 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0298others(10): Show | 13 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.952-12478C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839648 | ||||||
| chr7:152839659
|
C | T | 1 | a0001c0001t0002g0002 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.952-12467C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839659 | ||||||
| chr7:152839780
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.952-12346C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839780 | ||||||
| chr7:152839781
|
A | G | 19 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(16): Show | 19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.952-12345A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839781 | ||||||
| chr7:152839875
|
G | A | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.952-12251G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839875 | ||||||
| chr7:152839887
|
A | T | 1 | a0001c0001t0002g0102 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.952-12239A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839887 | ||||||
| chr7:152839923
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.952-12203C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839923 | ||||||
| chr7:152839947
|
C | A | 1 | a0001c0001t0007g0059 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.952-12179C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839947 | ||||||
| chr7:152840165
|
G | GGGTAGCT others(11): Show |
1 | a0001c0001t0007g0059 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.952-11956_952-1195 others(22): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152840165 | |||||
| chr7:152840175
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.952-11951A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840175 | ||||||
| chr7:152840183
|
G | A | 2 | a0001c0001t0001g0238a0001c0001t0001g0268 | 2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.952-11943G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840183 | ||||||
| chr7:152840315
|
C | T | 6 | a0001c0001t0001g0302a0001c0001t0002g0157a0001c0001t0002g0158others(3): Show | 6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.952-11811C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840315 | ||||||
| chr7:152840354
|
C | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.952-11772C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840354 | ||||||
| chr7:152840385
|
C | T | 18 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(15): Show | 18 | HG01099.hp2 HG01106.hp2 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.952-11741C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840385 | ||||||
| chr7:152840464
|
G | A | 58 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(55): Show | 58 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.952-11662G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840464 | ||||||
| chr7:152840480
|
C | G | 1 | a0001c0001t0001g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.952-11646C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840480 | ||||||
| chr7:152840481
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.952-11645T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840481 | ||||||
| chr7:152840485
|
A | G | 1 | a0001c0001t0001g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.952-11641A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840485 | ||||||
| chr7:152840494
|
C | T | 1 | a0001c0001t0002g0035 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.952-11632C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840494 | ||||||
| chr7:152840654
|
C | T | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.952-11472C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840654 | ||||||
| chr7:152840747
|
C | G | 1 | a0001c0001t0003g0168 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.952-11379C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840747 | ||||||
| chr7:152840766
|
G | A | 36 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(33): Show | 36 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.952-11360G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840766 | ||||||
| chr7:152840768
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.952-11358C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840768 | ||||||
| chr7:152840825
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.952-11301C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840825 | ||||||
| chr7:152840899
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.952-11227G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840899 | ||||||
| chr7:152840963
|
C | T | 5 | a0001c0001t0002g0007a0001c0001t0002g0155a0001c0001t0002g0156others(2): Show | 5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.952-11163C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840963 | ||||||
| chr7:152841057
|
A | G | 3 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0176 | 3 | HG01891.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.952-11069A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152841057 | ||||||
| chr7:152841153
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.952-10973C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152841153 | ||||||
| chr7:152841542
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.952-10584G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152841542 | ||||||
| chr7:152841733
|
C | T | 1 | a0001c0001t0002g0010 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.952-10393C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152841733 | ||||||
| chr7:152841777
|
T | G | 5 | a0001c0001t0002g0037a0001c0001t0002g0039a0001c0001t0002g0074others(2): Show | 5 | HG00423.hp1 HG00558.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.952-10349T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152841777 | ||||||
| chr7:152841794
|
G | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.952-10332G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152841794 | ||||||
| chr7:152841884
|
G | A | 2 | a0001c0001t0001g0216a0001c0001t0001g0250 | 2 | NA18948.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.952-10242G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152841884 | ||||||
| chr7:152842073
|
G | A | 2 | a0001c0001t0001g0257a0001c0001t0001g0267 | 2 | HG01243.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.952-10053G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152842073 | ||||||
| chr7:152842090
|
C | T | 38 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0113others(35): Show | 39 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.952-10036C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152842090 | ||||||
| chr7:152842239
|
A | G | 1 | a0001c0001t0002g0035 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.952-9887A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152842239 | ||||||
| chr7:152842286
|
G | A | 11 | a0001c0001t0003g0166a0001c0001t0003g0168a0001c0001t0003g0173others(8): Show | 11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.952-9840G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152842286 | ||||||
| chr7:152842521
|
G | T | 12 | a0001c0001t0001g0182a0001c0001t0003g0166a0001c0001t0003g0168others(9): Show | 12 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.952-9605G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152842521 | ||||||
| chr7:152842564
|
C | T | 16 | a0001c0001t0002g0007a0001c0001t0002g0155a0001c0001t0002g0156others(13): Show | 16 | HG01074.hp2 HG01099.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.952-9562C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152842564 | ||||||
| chr7:152842572
|
C | CT | 118 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(115): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.952-9553dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152842572 | |||||
| chr7:152842579
|
C | T | 16 | a0001c0001t0002g0007a0001c0001t0002g0155a0001c0001t0002g0156others(13): Show | 16 | HG01074.hp2 HG01099.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.952-9547C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152842579 | ||||||
| chr7:152842755
|
G | C | 38 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(35): Show | 38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.952-9371G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152842755 | ||||||
| chr7:152842856
|
T | C | 19 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(16): Show | 19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.952-9270T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152842856 | ||||||
| chr7:152842863
|
A | G | 2 | a0001c0001t0002g0171a0001c0001t0002g0172 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.952-9263A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152842863 | ||||||
| chr7:152842869
|
G | C | 1 | a0001c0001t0002g0178 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.952-9257G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152842869 | ||||||
| chr7:152843034
|
C | T | 253 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(250): Show | 255 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.952-9092C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152843034 | ||||||
| chr7:152843154
|
A | T | 38 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(35): Show | 38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.952-8972A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152843154 | ||||||
| chr7:152843229
|
T | C | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.952-8897T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152843229 | ||||||
| chr7:152843290
|
T | G | 118 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0214others(115): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.952-8836T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152843290 | ||||||
| chr7:152843392
|
C | T | 1 | a0001c0001t0002g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.952-8734C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152843392 | ||||||
| chr7:152843485
|
C | T | 1 | a0001c0001t0002g0064 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.952-8641C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152843485 | ||||||
| chr7:152843534
|
G | T | 22 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(19): Show | 22 | HG00423.hp2 HG00558.hp2 HG02132.hp1 others(19): Show |
intron_variant | MODIFIER | c.952-8592G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152843534 | ||||||
| chr7:152843827
|
C | T | 1 | a0001c0001t0002g0067 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.952-8299C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152843827 | ||||||
| chr7:152843914
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.952-8212C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152843914 | ||||||
| chr7:152843933
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.952-8193A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152843933 | ||||||
| chr7:152844045
|
A | G | 38 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0113others(35): Show | 39 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.952-8081A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844045 | ||||||
| chr7:152844160
|
C | A | 2 | a0001c0001t0005g0183a0001c0001t0008g0307 | 2 | HG02723.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.952-7966C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844160 | ||||||
| chr7:152844171
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.952-7955C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844171 | ||||||
| chr7:152844205
|
A | G | 254 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.952-7921A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844205 | ||||||
| chr7:152844340
|
G | A | 1 | a0001c0001t0002g0103 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.952-7786G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844340 | ||||||
| chr7:152844344
|
C | T | 3 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0018 | 3 | NA18989.hp2 NA19002.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.952-7782C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844344 | ||||||
| chr7:152844345
|
G | A | 1 | a0001c0001t0002g0103 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.952-7781G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844345 | ||||||
| chr7:152844349
|
C | T | 1 | a0001c0001t0002g0103 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.952-7777C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844349 | ||||||
| chr7:152844465
|
A | T | 2 | a0001c0001t0001g0300a0001c0001t0002g0103 | 2 | HG01070.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.952-7661A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844465 | ||||||
| chr7:152844569
|
T | C | 5 | a0001c0001t0001g0012a0001c0001t0001g0110a0001c0001t0001g0159others(2): Show | 5 | HG01070.hp2 HG03209.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.952-7557T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844569 | ||||||
| chr7:152844586
|
C | A | 6 | a0001c0001t0001g0012a0001c0001t0001g0110a0001c0001t0001g0159others(3): Show | 6 | HG01070.hp2 HG03209.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.952-7540C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844586 | ||||||
| chr7:152844606
|
G | T | 8 | a0001c0001t0001g0012a0001c0001t0001g0110a0001c0001t0001g0159others(5): Show | 8 | HG01070.hp2 HG03209.hp2 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.952-7520G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844606 | ||||||
| chr7:152844644
|
T | G | 15 | a0001c0001t0001g0200a0001c0001t0002g0023a0001c0001t0002g0024others(12): Show | 15 | HG00099.hp1 HG00738.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.952-7482T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844644 | ||||||
| chr7:152844668
|
C | A | 19 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(16): Show | 19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.952-7458C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844668 | ||||||
| chr7:152844690
|
T | C | 7 | a0001c0001t0002g0044a0001c0001t0002g0049a0001c0001t0002g0056others(4): Show | 7 | HG00438.hp1 HG02071.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.952-7436T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844690 | ||||||
| chr7:152844710
|
C | G | 3 | a0001c0001t0001g0302a0001c0001t0002g0026a0001c0004t0001g0303 | 3 | HG02257.hp1 HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.952-7416C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844710 | ||||||
| chr7:152844752
|
C | T | 116 | a0001c0001t0001g0003a0001c0001t0001g0184a0001c0001t0001g0186others(113): Show | 118 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.952-7374C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844752 | ||||||
| chr7:152844789
|
G | A | 187 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0113others(184): Show | 189 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(186): Show |
intron_variant | MODIFIER | c.952-7337G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844789 | ||||||
| chr7:152844811
|
T | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0015others(167): Show | 171 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.952-7315T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844811 | ||||||
| chr7:152844892
|
A | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0022others(127): Show | 132 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.952-7234A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844892 | ||||||
| chr7:152844984
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0159 | 2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.952-7142G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844984 | ||||||
| chr7:152844997
|
G | T | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.952-7129G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844997 | ||||||
| chr7:152845013
|
C | T | 29 | a0001c0001t0001g0014a0001c0001t0001g0110a0001c0001t0001g0117others(26): Show | 29 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.952-7113C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152845013 | ||||||
| chr7:152845102
|
T | C | 2 | a0001c0001t0001g0239a0001c0001t0001g0280 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.952-7024T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152845102 | ||||||
| chr7:152845113
|
G | A | 1 | a0001c0001t0002g0158 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.952-7013G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152845113 | ||||||
| chr7:152845190
|
GTAATA | G | 26 | a0001c0001t0001g0134a0001c0001t0001g0147a0001c0001t0001g0203others(23): Show | 26 | HG01070.hp1 HG01071.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.952-6928_952-6924d others(7): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152845190 | |||||
| chr7:152845204
|
G | A | 17 | a0001c0001t0001g0147a0001c0001t0001g0203a0001c0001t0001g0205others(14): Show | 17 | HG01070.hp1 HG01071.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.952-6922G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152845204 | ||||||
| chr7:152845239
|
G | T | 7 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0029others(4): Show | 7 | HG02055.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.952-6887G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152845239 | ||||||
| chr7:152845271
|
T | C | 3 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0176 | 3 | HG01891.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.952-6855T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152845271 | ||||||
| chr7:152845276
|
C | T | 1 | a0001c0002t0001g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.952-6850C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152845276 | ||||||
| chr7:152845296
|
A | C | 15 | a0001c0001t0001g0147a0001c0001t0001g0230a0001c0001t0001g0243others(12): Show | 15 | HG00423.hp1 HG01884.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.952-6830A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152845296 | ||||||
| chr7:152845374
|
G | A | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(3): Show | 6 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.952-6752G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152845374 | ||||||
| chr7:152845426
|
GT | G | 3 | a0001c0001t0001g0117a0001c0001t0001g0139a0001c0001t0002g0019 | 3 | HG02818.hp1 HG06807.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.952-6695delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152845426 | |||||
| chr7:152845482
|
C | T | 1 | a0001c0001t0002g0090 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.952-6644C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152845482 | ||||||
| chr7:152845531
|
C | T | 19 | a0001c0001t0001g0117a0001c0001t0001g0184a0001c0001t0001g0186others(16): Show | 19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.952-6595C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152845531 | ||||||
| chr7:152845588
|
C | A | 1 | a0001c0001t0001g0238 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.952-6538C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152845588 | ||||||
| chr7:152845598
|
T | C | 2 | a0001c0001t0002g0062a0001c0001t0002g0067 | 2 | NA20129.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.952-6528T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152845598 | ||||||
| chr7:152845603
|
C | G | 1 | a0001c0005t0001g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.952-6523C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152845603 | ||||||
| chr7:152845717
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.952-6409G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152845717 | ||||||
| chr7:152846124
|
CAGTCTGC others(24): Show |
C | 1 | a0001c0001t0001g0300 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.952-5964_952-5934d others(33): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152846124 | |||||
| chr7:152846207
|
G | A | 1 | a0001c0001t0001g0014 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.952-5919G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846207 | ||||||
| chr7:152846210
|
C | T | 1 | a0001c0001t0002g0101 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.952-5916C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846210 | ||||||
| chr7:152846245
|
G | A | 2 | a0001c0001t0002g0158a0001c0001t0002g0163 | 2 | HG03491.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.952-5881G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846245 | ||||||
| chr7:152846269
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.952-5857C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846269 | ||||||
| chr7:152846274
|
G | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.952-5852G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846274 | ||||||
| chr7:152846304
|
T | C | 3 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG01099.hp2 HG01106.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.952-5822T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846304 | ||||||
| chr7:152846335
|
C | T | 8 | a0001c0001t0003g0166a0001c0001t0003g0168a0001c0001t0003g0173others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.952-5791C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846335 | ||||||
| chr7:152846460
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.952-5666C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846460 | ||||||
| chr7:152846555
|
G | A | 1 | a0001c0001t0002g0067 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.952-5571G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846555 | ||||||
| chr7:152846597
|
C | CAGTGAGC others(55): Show |
20 | a0001c0001t0001g0117a0001c0001t0001g0184a0001c0001t0001g0186others(17): Show | 20 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.952-5521_952-5460d others(64): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152846597 | |||||
| chr7:152846597
|
CAGTGAGC others(24): Show |
C | 2 | a0001c0001t0002g0068a0001c0001t0002g0099 | 2 | HG01515.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.952-5490_952-5460d others(33): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152846597 | |||||
| chr7:152846620
|
GCA | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0288a0001c0001t0001g0291others(3): Show | 7 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.952-5505_952-5504d others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846620 | ||||||
| chr7:152846641
|
C | T | 3 | a0001c0001t0001g0182a0001c0001t0002g0007a0001c0001t0002g0055 | 3 | HG00735.hp2 HG02896.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.952-5485C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846641 | ||||||
| chr7:152846770
|
C | T | 1 | a0001c0001t0004g0169 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.952-5356C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846770 | ||||||
| chr7:152846785
|
T | TAGTGAGC others(55): Show |
1 | a0001c0001t0001g0181 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.952-5317_952-5256d others(64): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152846785 | |||||
| chr7:152846796
|
A | T | 1 | a0001c0001t0001g0267 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.952-5330A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846796 | ||||||
| chr7:152846895
|
C | T | 7 | a0001c0001t0001g0263a0001c0001t0001g0302a0001c0001t0002g0157others(4): Show | 7 | HG02630.hp2 HG03239.hp1 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.952-5231C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846895 | ||||||
| chr7:152846927
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.952-5199G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846927 | ||||||
| chr7:152846971
|
C | T | 123 | a0001c0001t0001g0003a0001c0001t0001g0129a0001c0001t0001g0200others(120): Show | 124 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.952-5155C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846971 | ||||||
| chr7:152846975
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.952-5151G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846975 | ||||||
| chr7:152846988
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.952-5138C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846988 | ||||||
| chr7:152846999
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.952-5127C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846999 | ||||||
| chr7:152847001
|
G | A | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.952-5125G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847001 | ||||||
| chr7:152847062
|
T | A | 123 | a0001c0001t0001g0003a0001c0001t0001g0129a0001c0001t0001g0200others(120): Show | 124 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.952-5064T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847062 | ||||||
| chr7:152847083
|
G | A | 2 | a0001c0001t0002g0026a0001c0001t0002g0065 | 2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.952-5043G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847083 | ||||||
| chr7:152847113
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.952-5013G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847113 | ||||||
| chr7:152847200
|
A | C | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.952-4926A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847200 | ||||||
| chr7:152847203
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.952-4923G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847203 | ||||||
| chr7:152847256
|
G | T | 5 | a0001c0001t0001g0182a0001c0001t0002g0007a0001c0001t0002g0156others(2): Show | 5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.952-4870G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847256 | ||||||
| chr7:152847436
|
A | G | 2 | a0001c0001t0002g0156a0001c0001t0002g0165 | 2 | HG01074.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.952-4690A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847436 | ||||||
| chr7:152847552
|
T | C | 244 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(241): Show | 246 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(243): Show |
intron_variant | MODIFIER | c.952-4574T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847552 | ||||||
| chr7:152847610
|
G | A | 1 | a0001c0001t0002g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.952-4516G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847610 | ||||||
| chr7:152847654
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.952-4472G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847654 | ||||||
| chr7:152847696
|
G | A | 3 | a0001c0001t0001g0289a0001c0001t0001g0293a0001c0001t0005g0290 | 3 | HG02809.hp2 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.952-4430G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847696 | ||||||
| chr7:152847873
|
C | A | 2 | a0001c0001t0001g0241a0001c0001t0002g0089 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.952-4253C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847873 | ||||||
| chr7:152847898
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.952-4228G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847898 | ||||||
| chr7:152847913
|
G | A | 1 | a0001c0001t0001g0257 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.952-4213G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847913 | ||||||
| chr7:152847939
|
G | A | 1 | a0001c0001t0002g0055 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.952-4187G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847939 | ||||||
| chr7:152847952
|
A | T | 1 | a0001c0001t0002g0027 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.952-4174A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847952 | ||||||
| chr7:152847992
|
A | G | 4 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0065others(1): Show | 4 | HG02280.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.952-4134A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847992 | ||||||
| chr7:152848085
|
G | GAAT | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0242others(1): Show | 4 | HG00735.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.952-4038_952-4036d others(5): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152848085 | |||||
| chr7:152848105
|
G | A | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.952-4021G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152848105 | ||||||
| chr7:152848266
|
G | A | 126 | a0001c0001t0001g0003a0001c0001t0001g0129a0001c0001t0001g0200others(123): Show | 127 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.952-3860G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152848266 | ||||||
| chr7:152848511
|
A | T | 1 | a0001c0001t0001g0267 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.952-3615A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152848511 | ||||||
| chr7:152848521
|
A | G | 21 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(18): Show | 21 | HG01099.hp2 HG01106.hp2 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.952-3605A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152848521 | ||||||
| chr7:152848614
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.952-3512G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152848614 | ||||||
| chr7:152848838
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.952-3288C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152848838 | ||||||
| chr7:152848957
|
G | C | 20 | a0001c0001t0001g0117a0001c0001t0001g0184a0001c0001t0001g0186others(17): Show | 20 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.952-3169G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152848957 | ||||||
| chr7:152849049
|
G | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.952-3077G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152849049 | ||||||
| chr7:152849140
|
A | C | 2 | a0001c0001t0002g0026a0001c0001t0002g0065 | 2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.952-2986A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152849140 | ||||||
| chr7:152849202
|
A | G | 20 | a0001c0001t0001g0117a0001c0001t0001g0184a0001c0001t0001g0186others(17): Show | 20 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.952-2924A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152849202 | ||||||
| chr7:152849237
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.952-2889C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152849237 | ||||||
| chr7:152849329
|
T | C | 41 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(38): Show | 41 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.952-2797T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152849329 | ||||||
| chr7:152849555
|
G | T | 5 | a0001c0001t0001g0182a0001c0001t0002g0007a0001c0001t0002g0156others(2): Show | 5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.952-2571G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152849555 | ||||||
| chr7:152849565
|
G | A | 2 | a0001c0001t0002g0027a0001c0001t0002g0097 | 2 | NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.952-2561G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152849565 | ||||||
| chr7:152849670
|
A | T | 6 | a0001c0001t0001g0302a0001c0001t0002g0157a0001c0001t0002g0158others(3): Show | 6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.952-2456A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152849670 | ||||||
| chr7:152849674
|
G | A | 1 | a0001c0005t0001g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.952-2452G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152849674 | ||||||
| chr7:152849717
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.952-2409A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152849717 | ||||||
| chr7:152849723
|
T | A | 1 | a0001c0001t0001g0110 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.952-2403T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152849723 | ||||||
| chr7:152849799
|
A | C | 9 | a0001c0001t0001g0296a0001c0001t0002g0002a0001c0001t0002g0019others(6): Show | 10 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.952-2327A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152849799 | ||||||
| chr7:152849920
|
T | C | 128 | a0001c0001t0001g0003a0001c0001t0001g0129a0001c0001t0001g0200others(125): Show | 129 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.952-2206T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152849920 | ||||||
| chr7:152850023
|
G | A | 3 | a0001c0001t0001g0289a0001c0001t0001g0293a0001c0001t0005g0290 | 3 | HG02809.hp2 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.952-2103G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152850023 | ||||||
| chr7:152850190
|
C | T | 5 | a0001c0001t0001g0207a0001c0001t0001g0239a0001c0001t0001g0240others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.952-1936C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152850190 | ||||||
| chr7:152850260
|
G | C | 1 | a0001c0001t0002g0055 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.952-1866G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152850260 | ||||||
| chr7:152850354
|
G | A | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.952-1772G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152850354 | ||||||
| chr7:152850490
|
G | A | 127 | a0001c0001t0001g0003a0001c0001t0001g0129a0001c0001t0001g0200others(124): Show | 128 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.952-1636G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152850490 | ||||||
| chr7:152850513
|
A | G | 3 | a0001c0001t0001g0289a0001c0001t0001g0293a0001c0001t0005g0290 | 3 | HG02809.hp2 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.952-1613A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152850513 | ||||||
| chr7:152850557
|
G | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.952-1569G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152850557 | ||||||
| chr7:152850713
|
C | T | 1 | a0001c0001t0002g0081 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.952-1413C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152850713 | ||||||
| chr7:152850763
|
AT | A | 21 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(18): Show | 21 | HG01099.hp2 HG01106.hp2 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.952-1354delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152850763 | |||||
| chr7:152850795
|
C | T | 1 | a0001c0001t0004g0170 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.952-1331C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152850795 | ||||||
| chr7:152850835
|
C | T | 20 | a0001c0001t0001g0117a0001c0001t0001g0184a0001c0001t0001g0186others(17): Show | 20 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.952-1291C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152850835 | ||||||
| chr7:152851285
|
A | G | 41 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(38): Show | 41 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.952-841A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152851285 | ||||||
| chr7:152851314
|
G | A | 3 | a0001c0001t0001g0289a0001c0001t0001g0293a0001c0001t0005g0290 | 3 | HG02809.hp2 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.952-812G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152851314 | ||||||
| chr7:152851332
|
C | T | 36 | a0001c0001t0001g0117a0001c0001t0001g0181a0001c0001t0001g0184others(33): Show | 36 | HG01109.hp1 HG01192.hp1 HG01952.hp1 others(33): Show |
intron_variant | MODIFIER | c.952-794C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152851332 | ||||||
| chr7:152851362
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.952-764T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152851362 | ||||||
| chr7:152851406
|
A | G | 41 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(38): Show | 41 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.952-720A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152851406 | ||||||
| chr7:152851428
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.952-698G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152851428 | ||||||
| chr7:152851506
|
C | T | 20 | a0001c0001t0001g0117a0001c0001t0001g0184a0001c0001t0001g0186others(17): Show | 20 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.952-620C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152851506 | ||||||
| chr7:152851545
|
C | T | 3 | a0001c0001t0001g0289a0001c0001t0001g0293a0001c0001t0005g0290 | 3 | HG02809.hp2 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.952-581C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152851545 | ||||||
| chr7:152851555
|
G | A | 16 | a0001c0001t0001g0181a0001c0001t0001g0289a0001c0001t0001g0293others(13): Show | 16 | HG01952.hp1 HG02145.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.952-571G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152851555 | ||||||
| chr7:152851647
|
G | C | 1 | a0001c0002t0001g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.952-479G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152851647 | ||||||
| chr7:152851766
|
C | G | 236 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(233): Show | 238 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(235): Show |
intron_variant | MODIFIER | c.952-360C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152851766 | ||||||
| chr7:152851839
|
T | C | 41 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(38): Show | 41 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.952-287T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152851839 | ||||||
| chr7:152851923
|
C | T | 5 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0242others(2): Show | 5 | HG00735.hp1 HG01891.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.952-203C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152851923 | ||||||
| chr7:152852022
|
C | T | 124 | a0001c0001t0001g0003a0001c0001t0001g0129a0001c0001t0001g0200others(121): Show | 125 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.952-104C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152852022 | ||||||
| chr7:152852084
|
G | A | 2 | a0001c0001t0005g0183a0001c0001t0008g0307 | 2 | HG02723.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.952-42G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152852084 | ||||||
| chr7:152852088
|
G | T | 18 | a0001c0001t0001g0117a0001c0001t0001g0184a0001c0001t0001g0186others(15): Show | 18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.952-38G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152852088 | ||||||
| chr7:152852273
|
G | A | 2 | a0001c0001t0001g0299a0001c0001t0001g0304 | 2 | HG01952.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1077+22G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152852273 | ||||||
| chr7:152852305
|
C | T | 4 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0304others(1): Show | 4 | HG01952.hp1 HG02622.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077+54C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152852305 | ||||||
| chr7:152852328
|
G | A | 16 | a0001c0001t0001g0181a0001c0001t0001g0289a0001c0001t0001g0293others(13): Show | 16 | HG01952.hp1 HG02145.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1077+77G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152852328 | ||||||
| chr7:152852347
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1077+96G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152852347 | ||||||
| chr7:152852407
|
G | A | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1077+156G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152852407 | ||||||
| chr7:152852464
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1077+213A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152852464 | ||||||
| chr7:152852813
|
A | T | 2 | a0001c0001t0002g0004a0001c0001t0002g0005 | 2 | NA18939.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1077+562A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152852813 | ||||||
| chr7:152852831
|
G | A | 1 | a0001c0001t0002g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1077+580G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152852831 | ||||||
| chr7:152852948
|
A | C | 1 | a0001c0001t0001g0128 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1078-546A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152852948 | ||||||
| chr7:152853054
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1078-440G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152853054 | ||||||
| chr7:152853059
|
G | A | 1 | a0001c0001t0002g0156 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1078-435G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152853059 | ||||||
| chr7:152853077
|
T | C | 42 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(39): Show | 42 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.1078-417T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152853077 | ||||||
| chr7:152853134
|
T | TA | 33 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204others(30): Show | 33 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1078-359dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr7 | 152853134 | |||||
| chr7:152853146
|
T | A | 4 | a0001c0001t0001g0296a0001c0001t0002g0002a0001c0001t0002g0179others(1): Show | 5 | HG01884.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1078-348T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152853146 | ||||||
| chr7:152853237
|
G | A | 6 | a0001c0001t0001g0302a0001c0001t0002g0157a0001c0001t0002g0158others(3): Show | 6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.1078-257G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152853237 | ||||||
| chr7:152853262
|
G | A | 1 | a0001c0001t0002g0086 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1078-232G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152853262 | ||||||
| chr7:152853295
|
G | C | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1078-199G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152853295 | ||||||
| chr7:152853359
|
T | C | 42 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(39): Show | 42 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.1078-135T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152853359 | ||||||
| chr7:152853413
|
C | T | 8 | a0001c0001t0003g0166a0001c0001t0003g0168a0001c0001t0003g0173others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1078-81C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152853413 | ||||||
| chr7:152853414
|
T | C | 235 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(232): Show | 237 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.1078-80T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152853414 | ||||||
| chr7:152853458
|
G | T | 1 | a0001c0001t0002g0072 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1078-36G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152853458 | ||||||
| chr7:152853464
|
G | T | 4 | a0001c0001t0001g0225a0001c0001t0001g0259a0001c0001t0001g0287others(1): Show | 4 | HG00099.hp1 HG01256.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1078-30G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152853464 | ||||||
| chr7:152853608
|
C | T | 1 | a0001c0001t0002g0054 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1161+31C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 11/11 | chr7 | 152853608 | ||||||
| chr7:152853780
|
G | A | 3 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0177 | 3 | HG01361.hp2 HG01934.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1161+203G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 11/11 | chr7 | 152853780 | ||||||
| chr7:152853780
|
G | T | 1 | a0001c0001t0001g0269 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1161+203G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 11/11 | chr7 | 152853780 | ||||||
| chr7:152853834
|
A | T | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1161+257A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 11/11 | chr7 | 152853834 | ||||||
| chr7:152853862
|
G | A | 1 | a0002c0006t0001g0189 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1161+285G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 11/11 | chr7 | 152853862 | ||||||
| chr7:152854231
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.1162-227C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 11/11 | chr7 | 152854231 |