Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 7220 |
|---|---|
| ensemblid | ENSG00000144935.17 |
| hgncid | 12333 |
| symbol | TRPC1 |
| name | transient receptor potential cation channel subfamily C member 1 |
| refseq_nuc | NM_001251845.2 |
| refseq_prot | NP_001238774.1 |
| ensembl_nuc | ENST00000476941.6 |
| ensembl_prot | ENSP00000419313.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 142724034 |
| end | 142807888 |
| strand | + |
| ver | v1.2 |
| region | chr3:142724034-142807888 |
| region5000 | chr3:142719034-142812888 |
| regionname0 | TRPC1_chr3_142724034_142807888 |
| regionname5000 | TRPC1_chr3_142719034_142812888 |
| 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 | 793 | 324 | 79 | 50 | 159 | 8 | 26 | 122 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0002 | 0/0 | 793 | 12 | 11 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0003 | 0/0 | 793 | 3 | 0 | 1 | 0 | 2 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0004 | 0/0 | 793 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| 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 | 2382 | 154 | 25 | 33 | 71 | 6 | 17 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| c0002 | 0/0 | 2382 | 71 | 5 | 10 | 49 | 2 | 5 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| c0003 | 0/0 | 2382 | 63 | 35 | 4 | 20 | 0 | 4 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| c0004 | 0/0 | 2382 | 22 | 2 | 2 | 18 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| c0005 | 0/0 | 2382 | 11 | 10 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| c0006 | 0/0 | 2382 | 11 | 11 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| c0007 | 0/0 | 2382 | 3 | 0 | 1 | 0 | 2 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| c0008 | 0/0 | 2382 | 2 | 1 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| c0009 | 0/0 | 2382 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| c0010 | 0/0 | 2382 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| c0011 | 0/0 | 2382 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| 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 | 2180 | 173 | 33 | 28 | 93 | 7 | 10 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| t0002 | 0/0 | 2180 | 50 | 10 | 6 | 27 | 0 | 7 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| t0003 | 0/0 | 2180 | 26 | 8 | 10 | 0 | 3 | 5 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| t0004 | 0/0 | 2180 | 22 | 0 | 0 | 20 | 0 | 2 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| t0005 | 0/0 | 2180 | 21 | 2 | 1 | 18 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| t0006 | 0/0 | 2180 | 20 | 15 | 2 | 1 | 0 | 2 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| t0007 | 0/0 | 2174 | 13 | 12 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| t0008 | 0/0 | 2180 | 7 | 7 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| t0009 | 0/0 | 2180 | 2 | 1 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| t0010 | 0/0 | 2180 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| t0011 | 0/0 | 2180 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| t0012 | 0/0 | 2180 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| t0013 | 0/0 | 2180 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| t0014 | 0/0 | 2180 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| t0015 | 0/0 | 2180 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| 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 | 7 | 0 | 0 | 7 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0011 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0159 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| 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 | 2382 | 154 | 25 | 33 | 71 | 6 | 17 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0001c0002 | 0/0 | 2382 | 71 | 5 | 10 | 49 | 2 | 5 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0001c0003 | 0/0 | 2382 | 63 | 35 | 4 | 20 | 0 | 4 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0001c0004 | 0/0 | 2382 | 22 | 2 | 2 | 18 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0001c0006 | 0/0 | 2382 | 11 | 11 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0001c0008 | 0/0 | 2382 | 2 | 1 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0001c0011 | 0/0 | 2382 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0002c0005 | 0/0 | 2382 | 11 | 10 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0002c0009 | 0/0 | 2382 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0003c0007 | 0/0 | 2382 | 3 | 0 | 1 | 0 | 2 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0004c0010 | 0/0 | 2382 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4561 | 73 | 4 | 15 | 44 | 3 | 5 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0001c0001t0002 | 0/0 | 4561 | 49 | 10 | 6 | 26 | 0 | 7 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0001c0001t0003 | 0/0 | 4561 | 21 | 3 | 10 | 0 | 3 | 5 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0001c0001t0007 | 0/0 | 4555 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0001c0001t0008 | 0/0 | 4561 | 7 | 7 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0001c0001t0012 | 0/0 | 4561 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0001c0001t0013 | 0/0 | 4561 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0001c0001t0015 | 0/0 | 4561 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0001c0002t0001 | 0/0 | 4561 | 71 | 5 | 10 | 49 | 2 | 5 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0001c0003t0001 | 0/0 | 4561 | 16 | 14 | 2 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0001c0003t0003 | 0/0 | 4561 | 5 | 5 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0001c0003t0004 | 0/0 | 4561 | 21 | 0 | 0 | 19 | 0 | 2 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0001c0003t0006 | 0/0 | 4561 | 19 | 14 | 2 | 1 | 0 | 2 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0001c0003t0010 | 0/0 | 4561 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0001c0003t0011 | 0/0 | 4561 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0001c0004t0005 | 0/0 | 4561 | 21 | 2 | 1 | 18 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0001c0004t0014 | 0/0 | 4561 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0001c0006t0001 | 0/0 | 4561 | 10 | 10 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0001c0006t0006 | 0/0 | 4561 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0001c0008t0009 | 0/0 | 4561 | 2 | 1 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0001c0011t0002 | 0/0 | 4561 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0002c0005t0007 | 0/0 | 4555 | 11 | 10 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0002c0009t0007 | 0/0 | 4555 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0003c0007t0001 | 0/0 | 4561 | 3 | 0 | 1 | 0 | 2 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| a0004c0010t0004 | 0/0 | 4561 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | copy fasta | chr3 | 142719034 | 142812888 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0011 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0159 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0003g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0007g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0008g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0008g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0008g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0008g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0008g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0008g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0008g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0012g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0013g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0001t0015g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0003g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0004g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0004g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0004g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0004g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0006g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0006g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0006g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0006g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0006g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0006g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0006g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0006g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0006g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0006g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0006g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0006g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0006g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0010g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0003t0011g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0004t0005g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0004t0005g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0004t0005g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0004t0005g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0004t0005g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0004t0005g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0004t0005g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0004t0005g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0004t0005g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0004t0005g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0004t0005g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0004t0005g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0004t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0004t0005g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0004t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0004t0005g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0004t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0004t0005g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0004t0014g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0006t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0006t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0006t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0006t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0006t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0006t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0006t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0006t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0006t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0006t0006g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0008t0009g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0008t0009g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0001c0011t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0002c0005t0007g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0002c0005t0007g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0002c0005t0007g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0002c0005t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0002c0005t0007g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0002c0005t0007g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0002c0005t0007g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0002c0005t0007g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0002c0005t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0002c0005t0007g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0002c0005t0007g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0002c0009t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0003c0007t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0003c0007t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0003c0007t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| a0004c0010t0004g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0186 | EUR | GBR | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0045 | EUR | GBR | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0289 | EUR | FIN | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0223 | EUR | FIN | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG00408 | hp2 | a0001 | c0001 | t0013 | g0087 | EAS | CHS | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0216 | EAS | CHS | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | CHS | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | CHS | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0218 | EAS | CHS | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0311 | EAS | CHS | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG00621 | hp1 | a0001 | c0003 | t0004 | g0060 | EAS | CHS | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG00642 | hp1 | a0001 | c0003 | t0006 | g0248 | AMR | PUR | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG00673 | hp2 | a0001 | c0004 | t0005 | g0266 | EAS | CHS | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0135 | AMR | PUR | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG00735 | hp2 | a0001 | c0003 | t0001 | g0254 | AMR | PUR | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0296 | AMR | PUR | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG00738 | hp2 | a0001 | c0004 | t0005 | g0265 | AMR | PUR | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0047 | AMR | PUR | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0292 | AMR | PUR | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01081 | hp1 | a0001 | c0001 | t0015 | g0155 | AMR | PUR | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0217 | AMR | PUR | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0294 | AMR | PUR | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0136 | AMR | PUR | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01109 | hp1 | a0001 | c0003 | t0001 | g0257 | AMR | PUR | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0110 | AMR | PUR | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0293 | AMR | PUR | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01175 | hp1 | a0001 | c0003 | t0006 | g0253 | AMR | PUR | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0222 | AMR | PUR | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01243 | hp2 | a0001 | c0001 | t0012 | g0151 | AMR | PUR | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01255 | hp1 | a0001 | c0008 | t0009 | g0025 | AMR | CLM | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0119 | AMR | CLM | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0046 | AMR | CLM | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | CLM | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0051 | AMR | CLM | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | CLM | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | CLM | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01346 | hp2 | a0001 | c0004 | t0014 | g0269 | AMR | CLM | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01358 | hp1 | a0003 | c0007 | t0001 | g0205 | AMR | CLM | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0298 | AMR | CLM | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0041 | AMR | CLM | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0286 | AMR | CLM | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0185 | EUR | IBS | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | IBS | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01884 | hp1 | a0001 | c0003 | t0003 | g0073 | AFR | ACB | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0287 | AFR | ACB | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0252 | AFR | ACB | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01891 | hp2 | a0001 | c0004 | t0005 | g0276 | AFR | ACB | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0221 | AMR | PEL | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0207 | AMR | PEL | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02027 | hp1 | a0001 | c0003 | t0004 | g0069 | EAS | KHV | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | KHV | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02040 | hp2 | a0004 | c0010 | t0004 | g0005 | EAS | KHV | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02055 | hp1 | a0001 | c0004 | t0005 | g0272 | AFR | ACB | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02055 | hp2 | a0002 | c0005 | t0007 | g0029 | AFR | ACB | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0312 | EAS | KHV | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | KHV | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | KHV | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0208 | EAS | KHV | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0142 | AFR | ACB | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02145 | hp2 | a0001 | c0001 | t0008 | g0138 | AFR | ACB | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CDX | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CDX | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | CDX | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | CDX | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02257 | hp1 | a0001 | c0003 | t0006 | g0238 | AFR | ACB | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | ACB | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02258 | hp1 | a0002 | c0005 | t0007 | g0026 | AFR | ACB | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02258 | hp2 | a0001 | c0003 | t0010 | g0022 | AFR | ACB | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0040 | AMR | PEL | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0211 | AMR | PEL | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02280 | hp1 | a0001 | c0003 | t0006 | g0015 | AFR | ACB | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02280 | hp2 | a0001 | c0006 | t0001 | g0303 | AFR | ACB | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | ACB | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02451 | hp2 | a0001 | c0006 | t0001 | g0305 | AFR | ACB | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | KHV | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02572 | hp1 | a0002 | c0005 | t0007 | g0027 | AFR | GWD | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | GWD | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02615 | hp1 | a0001 | c0003 | t0003 | g0074 | AFR | GWD | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | GWD | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02622 | hp2 | a0001 | c0003 | t0003 | g0006 | AFR | GWD | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0031 | AFR | GWD | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02630 | hp2 | a0001 | c0003 | t0006 | g0014 | AFR | GWD | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02647 | hp1 | a0001 | c0008 | t0009 | g0024 | AFR | GWD | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0209 | SAS | PJL | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0233 | SAS | PJL | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02717 | hp1 | a0002 | c0005 | t0007 | g0035 | AFR | GWD | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02717 | hp2 | a0001 | c0003 | t0006 | g0014 | AFR | GWD | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | GWD | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02723 | hp2 | a0001 | c0001 | t0008 | g0139 | AFR | GWD | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0290 | SAS | PJL | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0299 | AFR | GWD | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0033 | AFR | GWD | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0023 | AFR | GWD | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02886 | hp2 | a0001 | c0003 | t0006 | g0256 | AFR | GWD | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0016 | AFR | GWD | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02895 | hp2 | a0001 | c0001 | t0008 | g0143 | AFR | GWD | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02896 | hp1 | a0001 | c0001 | t0008 | g0156 | AFR | GWD | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0016 | AFR | GWD | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | GWD | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0262 | AFR | ESN | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02922 | hp2 | a0001 | c0006 | t0001 | g0308 | AFR | ESN | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0259 | AFR | ESN | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02965 | hp2 | a0001 | c0003 | t0006 | g0241 | AFR | ESN | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02970 | hp1 | a0001 | c0003 | t0003 | g0075 | AFR | ESN | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0032 | AFR | ESN | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02976 | hp1 | a0002 | c0005 | t0007 | g0055 | AFR | ESN | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0107 | AFR | ESN | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03017 | hp1 | a0001 | c0003 | t0006 | g0249 | SAS | PJL | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0131 | SAS | PJL | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03041 | hp1 | a0001 | c0003 | t0006 | g0250 | AFR | GWD | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0258 | AFR | GWD | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03098 | hp1 | a0001 | c0001 | t0008 | g0150 | AFR | MSL | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03098 | hp2 | a0002 | c0005 | t0007 | g0030 | AFR | MSL | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03130 | hp1 | a0001 | c0006 | t0001 | g0300 | AFR | ESN | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03130 | hp2 | a0001 | c0003 | t0006 | g0015 | AFR | ESN | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03225 | hp1 | a0002 | c0009 | t0007 | g0038 | AFR | MSL | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03225 | hp2 | a0001 | c0006 | t0001 | g0301 | AFR | MSL | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0224 | SAS | PJL | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03239 | hp2 | a0001 | c0003 | t0004 | g0064 | SAS | PJL | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0261 | AFR | MSL | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03453 | hp2 | a0001 | c0006 | t0001 | g0304 | AFR | MSL | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03486 | hp1 | a0001 | c0006 | t0001 | g0021 | AFR | MSL | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03486 | hp2 | a0001 | c0003 | t0006 | g0237 | AFR | MSL | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03516 | hp1 | a0002 | c0005 | t0007 | g0037 | AFR | ESN | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0263 | AFR | ESN | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03540 | hp1 | a0001 | c0003 | t0006 | g0239 | AFR | GWD | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0206 | AFR | GWD | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0234 | AFR | MSL | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03579 | hp2 | a0001 | c0003 | t0011 | g0251 | AFR | MSL | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0284 | SAS | PJL | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03688 | hp1 | a0001 | c0003 | t0006 | g0246 | SAS | STU | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0147 | SAS | STU | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03927 | hp1 | a0001 | c0003 | t0004 | g0067 | SAS | BEB | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0285 | SAS | BEB | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0123 | SAS | BEB | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0236 | SAS | STU | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0297 | SAS | STU | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0115 | SAS | STU | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0225 | SAS | STU | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0134 | SAS | STU | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | STU | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0140 | AFR | YRI | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | YRI | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18612 | hp1 | a0001 | c0004 | t0005 | g0018 | EAS | CHB | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | CHB | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0201 | EAS | CHB | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHB | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0240 | AFR | YRI | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18906 | hp2 | a0001 | c0003 | t0006 | g0244 | AFR | YRI | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18939 | hp1 | a0001 | c0004 | t0005 | g0271 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18945 | hp1 | a0001 | c0003 | t0004 | g0005 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18950 | hp2 | a0001 | c0003 | t0004 | g0065 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18952 | hp1 | a0001 | c0011 | t0002 | g0093 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18961 | hp2 | a0001 | c0003 | t0004 | g0004 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18963 | hp1 | a0001 | c0003 | t0004 | g0058 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18964 | hp2 | a0001 | c0003 | t0004 | g0061 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18969 | hp2 | a0001 | c0004 | t0005 | g0275 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18971 | hp2 | a0001 | c0003 | t0004 | g0002 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18972 | hp2 | a0001 | c0003 | t0004 | g0068 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18973 | hp1 | a0001 | c0003 | t0004 | g0002 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18982 | hp2 | a0001 | c0003 | t0004 | g0062 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18985 | hp1 | a0001 | c0004 | t0005 | g0277 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18986 | hp2 | a0001 | c0003 | t0004 | g0002 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18994 | hp2 | a0001 | c0004 | t0005 | g0017 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18998 | hp2 | a0001 | c0003 | t0004 | g0004 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA18999 | hp2 | a0001 | c0004 | t0005 | g0278 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19001 | hp1 | a0001 | c0003 | t0004 | g0056 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19001 | hp2 | a0001 | c0004 | t0005 | g0019 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19003 | hp2 | a0001 | c0004 | t0005 | g0017 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19005 | hp2 | a0001 | c0004 | t0005 | g0019 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19006 | hp2 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19007 | hp2 | a0001 | c0004 | t0005 | g0310 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19009 | hp2 | a0001 | c0003 | t0006 | g0245 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19010 | hp2 | a0001 | c0003 | t0004 | g0059 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19012 | hp2 | a0001 | c0004 | t0005 | g0274 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19043 | hp1 | a0001 | c0003 | t0006 | g0243 | AFR | LWK | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19043 | hp2 | a0002 | c0005 | t0007 | g0070 | AFR | LWK | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19058 | hp1 | a0001 | c0004 | t0005 | g0264 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19059 | hp1 | a0001 | c0003 | t0004 | g0057 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19062 | hp2 | a0001 | c0004 | t0005 | g0018 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19063 | hp1 | a0001 | c0004 | t0005 | g0270 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19065 | hp2 | a0001 | c0003 | t0004 | g0002 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19075 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19080 | hp1 | a0001 | c0003 | t0004 | g0063 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19083 | hp2 | a0001 | c0004 | t0005 | g0273 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19086 | hp1 | a0001 | c0004 | t0005 | g0267 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19086 | hp2 | a0001 | c0003 | t0004 | g0066 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19087 | hp2 | a0001 | c0004 | t0005 | g0268 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19240 | hp1 | a0001 | c0003 | t0001 | g0280 | AFR | YRI | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA19240 | hp2 | a0001 | c0006 | t0001 | g0302 | AFR | YRI | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA20129 | hp1 | a0001 | c0006 | t0001 | g0307 | AFR | ASW | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA20129 | hp2 | a0001 | c0003 | t0003 | g0006 | AFR | ASW | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0295 | EUR | TSI | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA20752 | hp2 | a0003 | c0007 | t0001 | g0235 | EUR | TSI | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0291 | EUR | TSI | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA20805 | hp2 | a0003 | c0007 | t0001 | g0204 | EUR | TSI | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0288 | SAS | GIH | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0114 | SAS | GIH | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01123 | hp1 | a0002 | c0005 | t0007 | g0036 | AMR | CLM | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02109 | hp2 | a0002 | c0005 | t0007 | g0034 | AFR | ACB | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02486 | hp1 | a0001 | c0006 | t0006 | g0306 | AFR | ACB | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02486 | hp2 | a0001 | c0003 | t0001 | g0260 | AFR | ACB | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02559 | hp1 | a0001 | c0003 | t0006 | g0255 | AFR | ACB | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | ACB | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03471 | hp1 | a0001 | c0006 | t0001 | g0021 | AFR | MSL | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG03471 | hp2 | a0001 | c0001 | t0008 | g0144 | AFR | MSL | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG06807 | hp1 | a0001 | c0003 | t0001 | g0242 | AFR | USA | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0279 | AFR | USA | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA20300 | hp1 | a0002 | c0005 | t0007 | g0028 | AFR | USA | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | USA | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA21309 | hp1 | a0001 | c0003 | t0006 | g0247 | AFR | LWK | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | LWK | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0011 | REF | REF | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0159 | REF | REF | TRPC1_chr3_142719034_142812888 | TRPC1 | chr3 | 142719034 | 142812888 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:142724599
|
G | A | 1 | a0003 | 3 | HG01358.hp1 NA20752.hp2 NA20805.hp2 |
missense_variant | MODERATE | c.40G>A | p.Ala14Thr | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/13 | 566/4561 | 40/2382 | 14/793 | chr3 | 142724599 | ||
| chr3:142724608
|
T | A | 1 | a0002 | 12 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
missense_variant | MODERATE | c.49T>A | p.Ser17Thr | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/13 | 575/4561 | 49/2382 | 17/793 | chr3 | 142724608 | ||
| chr3:142791123
|
G | T | 1 | a0004 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.1402G>T | p.Ala468Ser | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 8/13 | 1928/4561 | 1402/2382 | 468/793 | chr3 | 142791123 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:142748428
|
A | C | 1 | a0001c0008 | 2 | HG01255.hp1 HG02647.hp1 |
synonymous_variant | LOW | c.600A>C | p.Ala200Ala | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/13 | 1126/4561 | 600/2382 | 200/793 | chr3 | 142748428 | ||
| chr3:142784763
|
G | A | 9 | a0001c0002a0001c0003a0001c0004others(6): Show | 185 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(182): Show |
synonymous_variant | LOW | c.1020G>A | p.Ser340Ser | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/13 | 1546/4561 | 1020/2382 | 340/793 | chr3 | 142784763 | ||
| chr3:142804013
|
T | A | 1 | a0001c0006 | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
synonymous_variant | LOW | c.1794T>A | p.Ile598Ile | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 11/13 | 2320/4561 | 1794/2382 | 598/793 | chr3 | 142804013 | ||
| chr3:142804507
|
G | A | 4 | a0001c0002a0001c0006a0002c0009others(1): Show | 86 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(83): Show |
synonymous_variant | LOW | c.2031G>A | p.Thr677Thr | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/13 | 2557/4561 | 2031/2382 | 677/793 | chr3 | 142804507 | ||
| chr3:142806016
|
G | A | 9 | a0001c0002a0001c0003a0001c0006others(6): Show | 164 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(161): Show |
synonymous_variant | LOW | c.2163G>A | p.Arg721Arg | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 13/13 | 2689/4561 | 2163/2382 | 721/793 | chr3 | 142806016 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:142724053
|
G | A | 1 | a0001c0003t0010 | 1 | HG02258.hp2 | 5_prime_UTR_variant | MODIFIER | c.-507G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/13 | 507 | chr3 | 142724053 | |||||
| chr3:142724101
|
G | C | 2 | a0001c0001t0003a0001c0003t0003 | 26 | HG00323.hp1 HG00735.hp1 HG00738.hp1 others(23): Show |
5_prime_UTR_variant | MODIFIER | c.-459G>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/13 | 459 | chr3 | 142724101 | |||||
| chr3:142724233
|
C | A | 1 | a0001c0003t0011 | 1 | HG03579.hp2 | 5_prime_UTR_variant | MODIFIER | c.-327C>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/13 | 327 | chr3 | 142724233 | |||||
| chr3:142724241
|
G | C | 2 | a0001c0001t0008a0001c0001t0012 | 8 | HG01243.hp2 HG02145.hp2 HG02723.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-319G>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/13 | 319 | chr3 | 142724241 | |||||
| chr3:142724343
|
C | T | 1 | a0001c0008t0009 | 2 | HG01255.hp1 HG02647.hp1 |
5_prime_UTR_variant | MODIFIER | c.-217C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/13 | 217 | chr3 | 142724343 | |||||
| chr3:142724400
|
G | A | 2 | a0001c0003t0006a0001c0006t0006 | 20 | HG00642.hp1 HG01175.hp1 HG02257.hp1 others(17): Show |
5_prime_UTR_variant | MODIFIER | c.-160G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/13 | 160 | chr3 | 142724400 | |||||
| chr3:142724486
|
TGGGGTC | T | 3 | a0001c0001t0007a0002c0005t0007a0002c0009t0007 | 13 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-57_-52delTCGGGG | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/13 | 52 | INFO_REALIGN_3_PRIME | chr3 | 142724486 | ||||
| chr3:142806325
|
A | G | 1 | a0001c0001t0015 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*90A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 13/13 | 90 | chr3 | 142806325 | |||||
| chr3:142806465
|
T | C | 1 | a0001c0001t0013 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*230T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 13/13 | 230 | chr3 | 142806465 | |||||
| chr3:142806713
|
C | T | 1 | a0001c0004t0014 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*478C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 13/13 | 478 | chr3 | 142806713 | |||||
| chr3:142806788
|
A | G | 2 | a0001c0003t0004a0004c0010t0004 | 22 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*553A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 13/13 | 553 | chr3 | 142806788 | |||||
| chr3:142807385
|
G | A | 2 | a0001c0004t0005a0001c0004t0014 | 22 | HG00673.hp2 HG00738.hp2 HG01346.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1150G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 13/13 | 1150 | chr3 | 142807385 | |||||
| chr3:142807752
|
T | C | 4 | a0001c0001t0002a0001c0001t0012a0001c0001t0013others(1): Show | 52 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1517T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 13/13 | 1517 | chr3 | 142807752 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:142724875
|
TCTC | T | 4 | a0001c0003t0001g0023a0001c0003t0010g0022a0001c0008t0009g0024others(1): Show | 4 | HG01255.hp1 HG02258.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.172+148_172+150del others(3): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr3 | 142724875 | |||||
| chr3:142724878
|
C | T | 2 | a0001c0002t0001g0311a0001c0002t0001g0312 | 2 | HG00609.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.172+147C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142724878 | ||||||
| chr3:142724889
|
C | T | 1 | a0001c0004t0005g0310 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.172+158C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142724889 | ||||||
| chr3:142725221
|
A | C | 1 | a0001c0001t0002g0309 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.172+490A>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142725221 | ||||||
| chr3:142725291
|
G | A | 53 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0031others(50): Show | 64 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.172+560G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142725291 | ||||||
| chr3:142725372
|
G | T | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.172+641G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142725372 | ||||||
| chr3:142725581
|
A | G | 1 | a0002c0005t0007g0070 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.172+850A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142725581 | ||||||
| chr3:142725672
|
G | A | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.172+941G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142725672 | ||||||
| chr3:142725750
|
GACTA | G | 18 | a0001c0003t0004g0002a0001c0003t0004g0004a0001c0003t0004g0005others(15): Show | 22 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.172+1024_172+1027d others(6): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr3 | 142725750 | |||||
| chr3:142725783
|
G | T | 17 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(14): Show | 18 | HG00323.hp1 HG00738.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.172+1052G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142725783 | ||||||
| chr3:142725862
|
G | A | 2 | a0001c0003t0001g0023a0001c0003t0010g0022 | 2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.172+1131G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142725862 | ||||||
| chr3:142725890
|
C | T | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283 | 3 | HG01496.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.172+1159C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142725890 | ||||||
| chr3:142726173
|
G | A | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG00438.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.172+1442G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142726173 | ||||||
| chr3:142726231
|
CAG | C | 20 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(17): Show | 24 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.172+1502_172+1503d others(4): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr3 | 142726231 | |||||
| chr3:142726291
|
C | T | 1 | a0002c0005t0007g0055 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.172+1560C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142726291 | ||||||
| chr3:142726641
|
T | C | 18 | a0001c0003t0004g0002a0001c0003t0004g0004a0001c0003t0004g0005others(15): Show | 22 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.172+1910T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142726641 | ||||||
| chr3:142726846
|
T | C | 21 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(18): Show | 23 | HG00323.hp1 HG00738.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.172+2115T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142726846 | ||||||
| chr3:142726898
|
C | A | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283 | 3 | HG01496.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.172+2167C>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142726898 | ||||||
| chr3:142726933
|
T | C | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283 | 3 | HG01496.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.172+2202T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142726933 | ||||||
| chr3:142727268
|
G | A | 21 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(18): Show | 23 | HG00323.hp1 HG00738.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.172+2537G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142727268 | ||||||
| chr3:142727305
|
TA | T | 35 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0031others(32): Show | 42 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.172+2575delA | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142727305 | ||||||
| chr3:142727363
|
A | C | 149 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(146): Show | 166 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.172+2632A>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142727363 | ||||||
| chr3:142727451
|
A | G | 1 | a0001c0002t0001g0054 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.172+2720A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142727451 | ||||||
| chr3:142727801
|
A | G | 20 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0039others(17): Show | 27 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.172+3070A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142727801 | ||||||
| chr3:142727900
|
T | C | 40 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0199others(37): Show | 42 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.172+3169T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142727900 | ||||||
| chr3:142727982
|
TA | T | 11 | a0001c0003t0001g0280a0001c0006t0001g0021a0001c0006t0001g0300others(8): Show | 12 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.172+3263delA | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr3 | 142727982 | |||||
| chr3:142727996
|
T | C | 271 | a0001c0001t0001g0007a0001c0001t0001g0071a0001c0001t0001g0072others(268): Show | 297 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(294): Show |
intron_variant | MODIFIER | c.172+3265T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142727996 | ||||||
| chr3:142728001
|
G | T | 1 | a0001c0002t0001g0279 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.172+3270G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142728001 | ||||||
| chr3:142728335
|
CT | C | 165 | a0001c0001t0001g0077a0001c0001t0001g0158a0001c0001t0001g0281others(162): Show | 183 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.172+3619delT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr3 | 142728335 | |||||
| chr3:142728398
|
C | T | 2 | a0001c0003t0001g0023a0001c0003t0010g0022 | 2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.172+3667C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142728398 | ||||||
| chr3:142728406
|
G | A | 17 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(14): Show | 18 | HG00323.hp1 HG00738.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.172+3675G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142728406 | ||||||
| chr3:142728423
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.172+3692C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142728423 | ||||||
| chr3:142728424
|
G | T | 182 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(179): Show | 204 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.172+3693G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142728424 | ||||||
| chr3:142728444
|
G | C | 40 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0199others(37): Show | 42 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.172+3713G>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142728444 | ||||||
| chr3:142728548
|
C | A | 5 | a0002c0005t0007g0026a0002c0005t0007g0027a0002c0005t0007g0028others(2): Show | 5 | HG02055.hp2 HG02258.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.172+3817C>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142728548 | ||||||
| chr3:142728638
|
C | T | 19 | a0001c0004t0005g0017a0001c0004t0005g0018a0001c0004t0005g0019others(16): Show | 22 | HG00673.hp2 HG00738.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.172+3907C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142728638 | ||||||
| chr3:142728639
|
A | G | 2 | a0001c0003t0001g0023a0001c0003t0010g0022 | 2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.172+3908A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142728639 | ||||||
| chr3:142728702
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.172+3971C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142728702 | ||||||
| chr3:142728778
|
T | C | 31 | a0001c0001t0001g0007a0001c0001t0001g0071a0001c0001t0001g0072others(28): Show | 32 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.172+4047T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142728778 | ||||||
| chr3:142728842
|
G | C | 2 | a0001c0003t0006g0237a0001c0003t0006g0238 | 2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.172+4111G>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142728842 | ||||||
| chr3:142729036
|
G | A | 1 | a0001c0002t0001g0199 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.172+4305G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142729036 | ||||||
| chr3:142729155
|
C | T | 2 | a0001c0003t0001g0262a0001c0003t0001g0263 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.172+4424C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142729155 | ||||||
| chr3:142729236
|
T | G | 1 | a0001c0002t0001g0200 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.172+4505T>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142729236 | ||||||
| chr3:142729253
|
G | A | 4 | a0001c0002t0001g0199a0001c0002t0001g0201a0001c0002t0001g0202others(1): Show | 4 | NA18747.hp1 NA18989.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.172+4522G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142729253 | ||||||
| chr3:142729386
|
T | C | 1 | a0001c0001t0003g0284 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.172+4655T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142729386 | ||||||
| chr3:142729439
|
ATGTT | A | 40 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0199others(37): Show | 42 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.172+4712_172+4715d others(6): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr3 | 142729439 | |||||
| chr3:142729488
|
T | G | 33 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(30): Show | 36 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.172+4757T>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142729488 | ||||||
| chr3:142729500
|
G | T | 1 | a0001c0001t0008g0156 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.172+4769G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142729500 | ||||||
| chr3:142729600
|
C | T | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0015g0155 | 3 | HG01081.hp1 HG01358.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.172+4869C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142729600 | ||||||
| chr3:142729692
|
G | A | 1 | a0001c0003t0006g0239 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.172+4961G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142729692 | ||||||
| chr3:142729737
|
A | G | 97 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(94): Show | 109 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.172+5006A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142729737 | ||||||
| chr3:142729768
|
A | C | 1 | a0002c0009t0007g0038 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.172+5037A>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142729768 | ||||||
| chr3:142730033
|
G | A | 1 | a0001c0002t0001g0039 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.172+5302G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142730033 | ||||||
| chr3:142730142
|
A | T | 55 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0031others(52): Show | 65 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.172+5411A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142730142 | ||||||
| chr3:142730527
|
A | G | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.172+5796A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142730527 | ||||||
| chr3:142730606
|
G | GT | 137 | a0001c0001t0001g0103a0001c0001t0001g0197a0001c0001t0002g0152others(134): Show | 154 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.173-5759dupT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr3 | 142730606 | |||||
| chr3:142730606
|
G | GTT | 7 | a0001c0001t0003g0299a0001c0002t0001g0053a0001c0003t0001g0257others(4): Show | 7 | HG01109.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.173-5760_173-5759d others(4): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr3 | 142730606 | |||||
| chr3:142730606
|
GT | G | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.173-5759delT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr3 | 142730606 | |||||
| chr3:142730621
|
C | T | 11 | a0002c0005t0007g0026a0002c0005t0007g0027a0002c0005t0007g0028others(8): Show | 11 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.173-5758C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142730621 | ||||||
| chr3:142730629
|
A | G | 312 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0071others(309): Show | 339 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.173-5750A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142730629 | ||||||
| chr3:142730717
|
T | TTAA | 5 | a0001c0003t0001g0257a0001c0003t0001g0258a0001c0003t0001g0259others(2): Show | 5 | HG01109.hp1 HG02486.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.173-5661_173-5660i others(5): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr3 | 142730717 | |||||
| chr3:142730719
|
G | C | 5 | a0001c0003t0001g0257a0001c0003t0001g0258a0001c0003t0001g0259others(2): Show | 5 | HG01109.hp1 HG02486.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.173-5660G>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142730719 | ||||||
| chr3:142730719
|
G | GATC | 146 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(143): Show | 163 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.173-5657_173-5655d others(5): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr3 | 142730719 | |||||
| chr3:142730905
|
A | T | 1 | a0001c0004t0005g0278 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.173-5474A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142730905 | ||||||
| chr3:142731088
|
A | T | 2 | a0001c0003t0001g0023a0001c0003t0010g0022 | 2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.173-5291A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142731088 | ||||||
| chr3:142731146
|
A | C | 2 | a0001c0006t0001g0021a0001c0006t0001g0308 | 3 | HG02922.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.173-5233A>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142731146 | ||||||
| chr3:142731374
|
A | AT | 33 | a0001c0001t0001g0072a0001c0001t0001g0101a0001c0001t0001g0146others(30): Show | 34 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.173-4977dupT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr3 | 142731374 | |||||
| chr3:142731374
|
AT | A | 25 | a0001c0001t0001g0158a0001c0001t0002g0160a0001c0001t0003g0020others(22): Show | 30 | HG00323.hp1 HG00621.hp1 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.173-4977delT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr3 | 142731374 | |||||
| chr3:142731374
|
ATT | A | 9 | a0001c0003t0001g0254a0001c0003t0001g0261a0001c0003t0001g0263others(6): Show | 9 | HG00735.hp2 HG01175.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.173-4978_173-4977d others(4): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr3 | 142731374 | |||||
| chr3:142731374
|
ATTT | A | 23 | a0001c0003t0001g0016a0001c0003t0001g0252a0001c0003t0001g0257others(20): Show | 25 | HG00642.hp1 HG01109.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.173-4979_173-4977d others(5): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr3 | 142731374 | |||||
| chr3:142731374
|
ATTTT | A | 10 | a0001c0002t0001g0050a0001c0002t0001g0051a0001c0002t0001g0052others(7): Show | 11 | HG01258.hp1 HG01891.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.173-4980_173-4977d others(6): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr3 | 142731374 | |||||
| chr3:142731374
|
ATTTTT | A | 72 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(69): Show | 84 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.173-4981_173-4977d others(7): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr3 | 142731374 | |||||
| chr3:142731374
|
ATTTTTT | A | 6 | a0001c0002t0001g0031a0001c0002t0001g0032a0001c0002t0001g0201others(3): Show | 6 | HG02630.hp1 HG02818.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.173-4982_173-4977d others(8): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr3 | 142731374 | |||||
| chr3:142731374
|
ATTTTTTT | A | 12 | a0001c0001t0001g0078a0002c0005t0007g0026a0002c0005t0007g0027others(9): Show | 12 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.173-4983_173-4977d others(9): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr3 | 142731374 | |||||
| chr3:142731499
|
C | T | 18 | a0001c0003t0004g0002a0001c0003t0004g0004a0001c0003t0004g0005others(15): Show | 22 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.173-4880C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142731499 | ||||||
| chr3:142731545
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.173-4834C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142731545 | ||||||
| chr3:142731572
|
G | T | 149 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(146): Show | 166 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.173-4807G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142731572 | ||||||
| chr3:142731863
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | NA19002.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.173-4516G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142731863 | ||||||
| chr3:142731869
|
C | A | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.173-4510C>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142731869 | ||||||
| chr3:142731957
|
G | A | 169 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(166): Show | 190 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.173-4422G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142731957 | ||||||
| chr3:142732063
|
G | T | 95 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(92): Show | 107 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.173-4316G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142732063 | ||||||
| chr3:142732390
|
G | A | 5 | a0001c0003t0001g0257a0001c0003t0001g0258a0001c0003t0001g0259others(2): Show | 5 | HG01109.hp1 HG02486.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.173-3989G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142732390 | ||||||
| chr3:142732445
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.173-3934G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142732445 | ||||||
| chr3:142732687
|
A | G | 151 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(148): Show | 168 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.173-3692A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142732687 | ||||||
| chr3:142732723
|
C | T | 8 | a0001c0006t0001g0300a0001c0006t0001g0301a0001c0006t0001g0302others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.173-3656C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142732723 | ||||||
| chr3:142732782
|
A | G | 1 | a0001c0001t0001g0187 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.173-3597A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142732782 | ||||||
| chr3:142732815
|
A | G | 33 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(30): Show | 36 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.173-3564A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142732815 | ||||||
| chr3:142732917
|
G | A | 304 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0071others(301): Show | 331 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(328): Show |
intron_variant | MODIFIER | c.173-3462G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142732917 | ||||||
| chr3:142732917
|
G | T | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283 | 3 | HG01496.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.173-3462G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142732917 | ||||||
| chr3:142732966
|
C | CT | 124 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0001t0008g0138others(121): Show | 140 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.173-3400dupT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr3 | 142732966 | |||||
| chr3:142732966
|
CT | C | 43 | a0001c0001t0001g0197a0001c0003t0001g0016a0001c0003t0001g0240others(40): Show | 47 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.173-3400delT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr3 | 142732966 | |||||
| chr3:142733005
|
T | C | 2 | a0001c0002t0001g0031a0001c0002t0001g0032 | 2 | HG02630.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.173-3374T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142733005 | ||||||
| chr3:142733044
|
C | G | 20 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(17): Show | 24 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.173-3335C>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142733044 | ||||||
| chr3:142733117
|
G | T | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.173-3262G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142733117 | ||||||
| chr3:142733121
|
CTTTTAT | C | 95 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(92): Show | 107 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.173-3252_173-3247d others(8): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr3 | 142733121 | |||||
| chr3:142733449
|
T | A | 1 | a0001c0001t0001g0106 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.173-2930T>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142733449 | ||||||
| chr3:142733692
|
G | A | 20 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(17): Show | 24 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.173-2687G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142733692 | ||||||
| chr3:142733693
|
C | A | 20 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(17): Show | 24 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.173-2686C>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142733693 | ||||||
| chr3:142733751
|
A | C | 20 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(17): Show | 24 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.173-2628A>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142733751 | ||||||
| chr3:142733959
|
G | C | 17 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(14): Show | 18 | HG00323.hp1 HG00738.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.173-2420G>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142733959 | ||||||
| chr3:142734126
|
A | T | 1 | a0001c0001t0002g0100 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.173-2253A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142734126 | ||||||
| chr3:142734203
|
A | C | 184 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(181): Show | 206 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.173-2176A>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142734203 | ||||||
| chr3:142734552
|
CAA | C | 3 | a0001c0001t0002g0010a0001c0001t0002g0137a0001c0001t0002g0149 | 4 | NA18973.hp2 NA19006.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.173-1826_173-1825d others(4): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142734552 | ||||||
| chr3:142734759
|
G | C | 2 | a0001c0006t0001g0021a0001c0006t0001g0308 | 3 | HG02922.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.173-1620G>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142734759 | ||||||
| chr3:142734787
|
T | TA | 9 | a0001c0001t0003g0291a0001c0001t0003g0292a0001c0001t0003g0293others(6): Show | 9 | HG00738.hp1 HG01074.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.173-1581dupA | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr3 | 142734787 | |||||
| chr3:142734787
|
TA | T | 11 | a0001c0003t0001g0242a0001c0006t0001g0021a0001c0006t0001g0300others(8): Show | 12 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.173-1581delA | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr3 | 142734787 | |||||
| chr3:142734788
|
A | T | 20 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(17): Show | 24 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.173-1591A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142734788 | ||||||
| chr3:142734848
|
C | T | 2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG01496.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.173-1531C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142734848 | ||||||
| chr3:142735002
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.173-1377G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142735002 | ||||||
| chr3:142735036
|
GTGTC | G | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.173-1336_173-1333d others(6): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr3 | 142735036 | |||||
| chr3:142735043
|
T | G | 19 | a0001c0004t0005g0017a0001c0004t0005g0018a0001c0004t0005g0019others(16): Show | 22 | HG00673.hp2 HG00738.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.173-1336T>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142735043 | ||||||
| chr3:142735447
|
A | G | 20 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(17): Show | 24 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.173-932A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142735447 | ||||||
| chr3:142735506
|
A | G | 1 | a0001c0003t0006g0255 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.173-873A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142735506 | ||||||
| chr3:142735572
|
A | G | 181 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(178): Show | 203 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.173-807A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142735572 | ||||||
| chr3:142735651
|
C | T | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.173-728C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142735651 | ||||||
| chr3:142735780
|
G | A | 19 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0039others(16): Show | 26 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.173-599G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142735780 | ||||||
| chr3:142735836
|
C | T | 1 | a0001c0002t0001g0279 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.173-543C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142735836 | ||||||
| chr3:142735991
|
A | G | 11 | a0002c0005t0007g0026a0002c0005t0007g0027a0002c0005t0007g0028others(8): Show | 11 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.173-388A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142735991 | ||||||
| chr3:142736195
|
C | T | 2 | a0001c0001t0003g0135a0001c0001t0003g0136 | 2 | HG00735.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.173-184C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142736195 | ||||||
| chr3:142736196
|
G | A | 1 | a0001c0004t0005g0265 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.173-183G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | chr3 | 142736196 | ||||||
| chr3:142736196
|
G | GT | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.173-182dupT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr3 | 142736196 | |||||
| chr3:142736643
|
T | A | 1 | a0001c0002t0001g0207 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.327+110T>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142736643 | ||||||
| chr3:142736649
|
T | G | 1 | a0001c0001t0001g0165 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.327+116T>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142736649 | ||||||
| chr3:142736761
|
T | A | 2 | a0001c0003t0006g0243a0001c0003t0006g0253 | 2 | HG01175.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.327+228T>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142736761 | ||||||
| chr3:142736916
|
A | G | 2 | a0003c0007t0001g0204a0003c0007t0001g0235 | 2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.327+383A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142736916 | ||||||
| chr3:142737103
|
G | A | 1 | a0002c0005t0007g0070 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.327+570G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142737103 | ||||||
| chr3:142737217
|
C | CT | 42 | a0001c0001t0001g0103a0001c0002t0001g0012a0001c0002t0001g0013others(39): Show | 44 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.327+697dupT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr3 | 142737217 | |||||
| chr3:142737217
|
CT | C | 11 | a0001c0004t0005g0264a0001c0006t0001g0021a0001c0006t0001g0300others(8): Show | 12 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.327+697delT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr3 | 142737217 | |||||
| chr3:142737324
|
T | TTA | 89 | a0001c0001t0001g0007a0001c0001t0001g0071a0001c0001t0001g0072others(86): Show | 93 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.327+803_327+804dup others(2): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr3 | 142737324 | |||||
| chr3:142737330
|
A | ATATG | 56 | a0001c0001t0003g0291a0001c0001t0003g0292a0001c0001t0003g0293others(53): Show | 64 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.327+800_327+801ins others(4): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr3 | 142737330 | |||||
| chr3:142737330
|
A | ATATGTAT others(1): Show |
43 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(40): Show | 45 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.327+800_327+801ins others(8): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr3 | 142737330 | |||||
| chr3:142737330
|
A | ATATGTAT others(5): Show |
6 | a0001c0002t0001g0013a0001c0002t0001g0229a0001c0002t0001g0230others(3): Show | 7 | HG02523.hp2 HG02698.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.327+800_327+801ins others(12): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr3 | 142737330 | |||||
| chr3:142737330
|
A | ATATGTAT others(9): Show |
1 | a0001c0002t0001g0234 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.327+800_327+801ins others(16): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr3 | 142737330 | |||||
| chr3:142737334
|
A | ATATATG | 4 | a0001c0001t0001g0077a0001c0001t0001g0281a0001c0001t0001g0282others(1): Show | 4 | HG01433.hp2 HG01496.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+804_327+805ins others(6): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr3 | 142737334 | |||||
| chr3:142737334
|
A | ATATG | 11 | a0001c0003t0003g0073a0001c0006t0001g0021a0001c0006t0001g0300others(8): Show | 12 | HG01884.hp1 HG02280.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.327+825_327+828dup others(4): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr3 | 142737334 | |||||
| chr3:142737334
|
A | ATATGTAT others(1): Show |
19 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(16): Show | 23 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.327+821_327+828dup others(8): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr3 | 142737334 | |||||
| chr3:142737334
|
A | ATATGTAT others(5): Show |
1 | a0001c0003t0004g0067 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.327+817_327+828dup others(12): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr3 | 142737334 | |||||
| chr3:142737334
|
A | G | 148 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(145): Show | 165 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.327+801A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142737334 | ||||||
| chr3:142737354
|
G | GTATC | 20 | a0001c0002t0001g0279a0001c0004t0005g0017a0001c0004t0005g0018others(17): Show | 23 | HG00673.hp2 HG00738.hp2 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.327+824_327+825ins others(4): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr3 | 142737354 | |||||
| chr3:142737402
|
T | TA | 23 | a0001c0001t0001g0103a0001c0001t0003g0020a0001c0001t0003g0284others(20): Show | 25 | HG00323.hp1 HG00738.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.327+879dupA | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr3 | 142737402 | |||||
| chr3:142737584
|
T | G | 19 | a0001c0004t0005g0017a0001c0004t0005g0018a0001c0004t0005g0019others(16): Show | 22 | HG00673.hp2 HG00738.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.327+1051T>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142737584 | ||||||
| chr3:142737833
|
G | A | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.327+1300G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142737833 | ||||||
| chr3:142737858
|
C | G | 1 | a0001c0001t0001g0182 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.327+1325C>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142737858 | ||||||
| chr3:142737874
|
A | G | 1 | a0002c0005t0007g0070 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.327+1341A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142737874 | ||||||
| chr3:142737964
|
G | C | 1 | a0001c0004t0005g0266 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.327+1431G>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142737964 | ||||||
| chr3:142738372
|
G | C | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283 | 3 | HG01496.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.327+1839G>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142738372 | ||||||
| chr3:142738487
|
C | T | 24 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0031others(21): Show | 31 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.327+1954C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142738487 | ||||||
| chr3:142738809
|
AAGTATC | A | 5 | a0001c0003t0001g0257a0001c0003t0001g0258a0001c0003t0001g0259others(2): Show | 5 | HG01109.hp1 HG02486.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+2280_327+2285d others(8): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr3 | 142738809 | |||||
| chr3:142738915
|
T | C | 181 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(178): Show | 203 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.327+2382T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142738915 | ||||||
| chr3:142739032
|
C | G | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283 | 3 | HG01496.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.327+2499C>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142739032 | ||||||
| chr3:142739075
|
G | A | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283 | 3 | HG01496.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.327+2542G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142739075 | ||||||
| chr3:142739104
|
T | A | 2 | a0001c0008t0009g0024a0001c0008t0009g0025 | 2 | HG01255.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.327+2571T>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142739104 | ||||||
| chr3:142739132
|
G | A | 1 | a0001c0002t0001g0208 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.327+2599G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142739132 | ||||||
| chr3:142739135
|
C | T | 18 | a0001c0003t0004g0002a0001c0003t0004g0004a0001c0003t0004g0005others(15): Show | 22 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.327+2602C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142739135 | ||||||
| chr3:142739418
|
T | A | 1 | a0002c0009t0007g0038 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.327+2885T>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142739418 | ||||||
| chr3:142739669
|
G | A | 2 | a0001c0003t0001g0023a0001c0003t0010g0022 | 2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.327+3136G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142739669 | ||||||
| chr3:142739864
|
G | A | 181 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(178): Show | 203 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.327+3331G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142739864 | ||||||
| chr3:142739877
|
T | G | 21 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(18): Show | 23 | HG00323.hp1 HG00738.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.327+3344T>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142739877 | ||||||
| chr3:142739963
|
C | T | 1 | a0002c0005t0007g0037 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.327+3430C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142739963 | ||||||
| chr3:142740141
|
T | C | 1 | a0001c0002t0001g0236 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.328-3344T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142740141 | ||||||
| chr3:142740155
|
G | T | 1 | a0001c0001t0002g0160 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.328-3330G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142740155 | ||||||
| chr3:142740289
|
A | G | 1 | a0001c0001t0001g0195 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.328-3196A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142740289 | ||||||
| chr3:142740311
|
C | G | 18 | a0001c0003t0004g0002a0001c0003t0004g0004a0001c0003t0004g0005others(15): Show | 22 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.328-3174C>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142740311 | ||||||
| chr3:142740312
|
T | C | 1 | a0001c0004t0005g0267 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.328-3173T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142740312 | ||||||
| chr3:142740728
|
T | C | 19 | a0001c0004t0005g0017a0001c0004t0005g0018a0001c0004t0005g0019others(16): Show | 22 | HG00673.hp2 HG00738.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.328-2757T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142740728 | ||||||
| chr3:142740973
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.328-2512G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142740973 | ||||||
| chr3:142741064
|
G | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG03669.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.328-2421G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142741064 | ||||||
| chr3:142741121
|
T | C | 1 | a0001c0001t0001g0080 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.328-2364T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142741121 | ||||||
| chr3:142741181
|
T | TATAACTA others(307): Show |
1 | a0002c0005t0007g0055 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.328-2288_328-2287i others(316): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr3 | 142741181 | |||||
| chr3:142741181
|
T | TATAACTA others(307): Show |
1 | a0001c0002t0001g0236 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.328-2288_328-2287i others(316): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr3 | 142741181 | |||||
| chr3:142741181
|
T | TATAACTA others(308): Show |
85 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(82): Show | 97 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.328-2288_328-2287i others(317): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr3 | 142741181 | |||||
| chr3:142741181
|
T | TATAACTA others(309): Show |
9 | a0001c0002t0001g0039a0001c0002t0001g0279a0001c0002t0001g0312others(6): Show | 9 | HG01123.hp1 HG02055.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.328-2288_328-2287i others(318): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr3 | 142741181 | |||||
| chr3:142741181
|
T | TATAACTA others(311): Show |
1 | a0003c0007t0001g0205 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.328-2288_328-2287i others(320): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr3 | 142741181 | |||||
| chr3:142741235
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.328-2250A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142741235 | ||||||
| chr3:142741325
|
A | G | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.328-2160A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142741325 | ||||||
| chr3:142741417
|
C | T | 2 | a0001c0003t0001g0023a0001c0003t0010g0022 | 2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.328-2068C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142741417 | ||||||
| chr3:142741625
|
ATTCTT | A | 20 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(17): Show | 24 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.328-1857_328-1853d others(7): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr3 | 142741625 | |||||
| chr3:142741956
|
A | C | 1 | a0001c0003t0006g0237 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.328-1529A>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142741956 | ||||||
| chr3:142742118
|
G | A | 2 | a0001c0003t0001g0023a0001c0003t0010g0022 | 2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.328-1367G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142742118 | ||||||
| chr3:142742162
|
C | CA | 143 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(140): Show | 159 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.328-1309dupA | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr3 | 142742162 | |||||
| chr3:142742162
|
C | CAA | 6 | a0001c0003t0003g0006a0001c0003t0003g0073a0001c0003t0003g0074others(3): Show | 7 | HG01884.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.328-1310_328-1309d others(4): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr3 | 142742162 | |||||
| chr3:142742233
|
T | A | 6 | a0001c0001t0008g0138a0001c0001t0008g0139a0001c0001t0008g0140others(3): Show | 6 | HG01243.hp2 HG02145.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.328-1252T>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142742233 | ||||||
| chr3:142742428
|
G | A | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.328-1057G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142742428 | ||||||
| chr3:142742530
|
A | G | 181 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(178): Show | 203 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.328-955A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142742530 | ||||||
| chr3:142742538
|
C | T | 1 | a0001c0002t0001g0234 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.328-947C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142742538 | ||||||
| chr3:142742574
|
G | A | 3 | a0001c0003t0001g0016a0001c0003t0001g0252a0001c0003t0011g0251 | 4 | HG01891.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-911G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142742574 | ||||||
| chr3:142742838
|
C | G | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.328-647C>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142742838 | ||||||
| chr3:142742960
|
A | C | 31 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(28): Show | 34 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.328-525A>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142742960 | ||||||
| chr3:142743133
|
G | T | 1 | a0001c0002t0001g0234 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.328-352G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142743133 | ||||||
| chr3:142743174
|
GA | G | 21 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(18): Show | 23 | HG00323.hp1 HG00738.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.328-303delA | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr3 | 142743174 | |||||
| chr3:142743229
|
T | C | 20 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(17): Show | 24 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.328-256T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142743229 | ||||||
| chr3:142743294
|
ATT | A | 42 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0104others(39): Show | 44 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.328-190_328-189del others(2): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 2/12 | chr3 | 142743294 | ||||||
| chr3:142744316
|
G | T | 18 | a0001c0003t0004g0002a0001c0003t0004g0004a0001c0003t0004g0005others(15): Show | 22 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.429+730G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142744316 | ||||||
| chr3:142744357
|
G | C | 2 | a0001c0006t0001g0021a0001c0006t0001g0308 | 3 | HG02922.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.429+771G>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142744357 | ||||||
| chr3:142744500
|
A | C | 33 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(30): Show | 36 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.429+914A>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142744500 | ||||||
| chr3:142744531
|
T | C | 1 | a0001c0002t0001g0209 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.429+945T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142744531 | ||||||
| chr3:142744565
|
T | C | 2 | a0001c0008t0009g0024a0001c0008t0009g0025 | 2 | HG01255.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.429+979T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142744565 | ||||||
| chr3:142744642
|
C | G | 11 | a0002c0005t0007g0026a0002c0005t0007g0027a0002c0005t0007g0028others(8): Show | 11 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.429+1056C>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142744642 | ||||||
| chr3:142744660
|
G | A | 2 | a0001c0001t0003g0291a0001c0001t0003g0292 | 2 | HG01074.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.429+1074G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142744660 | ||||||
| chr3:142744884
|
G | C | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.429+1298G>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142744884 | ||||||
| chr3:142744913
|
G | C | 33 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(30): Show | 36 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.429+1327G>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142744913 | ||||||
| chr3:142744974
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.429+1388G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142744974 | ||||||
| chr3:142745138
|
A | G | 181 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(178): Show | 203 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.429+1552A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142745138 | ||||||
| chr3:142745185
|
A | AC | 21 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(18): Show | 23 | HG00323.hp1 HG00738.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.429+1601dupC | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr3 | 142745185 | |||||
| chr3:142745219
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.429+1633T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142745219 | ||||||
| chr3:142745236
|
A | C | 151 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(148): Show | 168 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.429+1650A>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142745236 | ||||||
| chr3:142745238
|
C | A | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.429+1652C>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142745238 | ||||||
| chr3:142745378
|
C | T | 1 | a0001c0002t0001g0048 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.429+1792C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142745378 | ||||||
| chr3:142745410
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.429+1824G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142745410 | ||||||
| chr3:142745557
|
T | C | 18 | a0001c0003t0004g0002a0001c0003t0004g0004a0001c0003t0004g0005others(15): Show | 22 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.429+1971T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142745557 | ||||||
| chr3:142745604
|
G | A | 1 | a0001c0001t0001g0281 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.429+2018G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142745604 | ||||||
| chr3:142745817
|
G | A | 2 | a0001c0003t0003g0006a0001c0003t0003g0074 | 3 | HG02615.hp1 HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.429+2231G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142745817 | ||||||
| chr3:142745819
|
G | A | 1 | a0001c0002t0001g0279 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.429+2233G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142745819 | ||||||
| chr3:142745882
|
G | C | 181 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(178): Show | 203 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.429+2296G>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142745882 | ||||||
| chr3:142746000
|
A | G | 18 | a0001c0004t0005g0017a0001c0004t0005g0018a0001c0004t0005g0019others(15): Show | 21 | HG00673.hp2 HG00738.hp2 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.430-2258A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142746000 | ||||||
| chr3:142746056
|
G | A | 1 | a0001c0001t0007g0107 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.430-2202G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142746056 | ||||||
| chr3:142746087
|
T | G | 1 | a0001c0001t0001g0196 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.430-2171T>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142746087 | ||||||
| chr3:142746282
|
T | C | 1 | a0001c0001t0002g0108 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.430-1976T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142746282 | ||||||
| chr3:142746631
|
A | C | 1 | a0001c0001t0002g0134 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.430-1627A>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142746631 | ||||||
| chr3:142746749
|
A | G | 2 | a0001c0006t0001g0021a0001c0006t0001g0308 | 3 | HG02922.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.430-1509A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142746749 | ||||||
| chr3:142746782
|
C | T | 20 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(17): Show | 24 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.430-1476C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142746782 | ||||||
| chr3:142746806
|
C | G | 1 | a0001c0001t0001g0181 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.430-1452C>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142746806 | ||||||
| chr3:142746893
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.430-1365A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142746893 | ||||||
| chr3:142746938
|
C | G | 181 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(178): Show | 203 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.430-1320C>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142746938 | ||||||
| chr3:142747108
|
C | T | 5 | a0001c0003t0001g0257a0001c0003t0001g0258a0001c0003t0001g0259others(2): Show | 5 | HG01109.hp1 HG02486.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.430-1150C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142747108 | ||||||
| chr3:142747342
|
CA | C | 116 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(113): Show | 127 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.430-907delA | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr3 | 142747342 | |||||
| chr3:142747346
|
A | G | 8 | a0001c0006t0001g0300a0001c0006t0001g0301a0001c0006t0001g0302others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.430-912A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142747346 | ||||||
| chr3:142747452
|
C | T | 2 | a0001c0004t0005g0019a0001c0004t0005g0278 | 3 | NA18999.hp2 NA19001.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.430-806C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142747452 | ||||||
| chr3:142747494
|
A | C | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.430-764A>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142747494 | ||||||
| chr3:142747542
|
G | A | 1 | a0001c0002t0001g0206 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.430-716G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142747542 | ||||||
| chr3:142747717
|
T | C | 20 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(17): Show | 24 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.430-541T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142747717 | ||||||
| chr3:142747973
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.430-285T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 3/12 | chr3 | 142747973 | ||||||
| chr3:142748468
|
C | T | 42 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0104others(39): Show | 44 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(41): Show |
splice_region_variant&intron_variant | LOW | c.632+8C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142748468 | ||||||
| chr3:142748581
|
G | A | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283 | 3 | HG01496.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.632+121G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142748581 | ||||||
| chr3:142748764
|
G | A | 24 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0031others(21): Show | 31 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.632+304G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142748764 | ||||||
| chr3:142748925
|
T | C | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.632+465T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142748925 | ||||||
| chr3:142749128
|
G | A | 20 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(17): Show | 24 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.632+668G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142749128 | ||||||
| chr3:142749167
|
G | A | 14 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(11): Show | 15 | HG00735.hp2 HG01109.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.632+707G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142749167 | ||||||
| chr3:142749206
|
C | T | 14 | a0001c0003t0001g0023a0001c0003t0001g0261a0001c0003t0010g0022others(11): Show | 14 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.632+746C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142749206 | ||||||
| chr3:142749218
|
G | A | 33 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(30): Show | 36 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.632+758G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142749218 | ||||||
| chr3:142749504
|
T | G | 181 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(178): Show | 203 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.632+1044T>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142749504 | ||||||
| chr3:142749553
|
T | C | 181 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(178): Show | 203 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.632+1093T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142749553 | ||||||
| chr3:142749563
|
G | C | 97 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(94): Show | 109 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.632+1103G>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142749563 | ||||||
| chr3:142749645
|
A | T | 1 | a0001c0001t0002g0148 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.632+1185A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142749645 | ||||||
| chr3:142749653
|
C | T | 97 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(94): Show | 109 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.632+1193C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142749653 | ||||||
| chr3:142749960
|
G | A | 4 | a0001c0003t0003g0006a0001c0003t0003g0073a0001c0003t0003g0074others(1): Show | 5 | HG01884.hp1 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.632+1500G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142749960 | ||||||
| chr3:142749975
|
G | A | 1 | a0001c0001t0002g0081 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.632+1515G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142749975 | ||||||
| chr3:142750060
|
A | C | 1 | a0002c0009t0007g0038 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.632+1600A>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142750060 | ||||||
| chr3:142750254
|
G | A | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.632+1794G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142750254 | ||||||
| chr3:142750299
|
C | A | 1 | a0001c0004t0005g0265 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.632+1839C>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142750299 | ||||||
| chr3:142750304
|
A | T | 1 | a0002c0005t0007g0070 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.632+1844A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142750304 | ||||||
| chr3:142750433
|
G | T | 20 | a0001c0002t0001g0279a0001c0004t0005g0017a0001c0004t0005g0018others(17): Show | 23 | HG00673.hp2 HG00738.hp2 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.632+1973G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142750433 | ||||||
| chr3:142750507
|
T | C | 1 | a0001c0002t0001g0040 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.632+2047T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142750507 | ||||||
| chr3:142750632
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.632+2172G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142750632 | ||||||
| chr3:142750764
|
A | G | 20 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(17): Show | 24 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.632+2304A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142750764 | ||||||
| chr3:142750788
|
C | T | 3 | a0001c0003t0001g0023a0001c0003t0010g0022a0002c0005t0007g0070 | 3 | HG02258.hp2 HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.632+2328C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142750788 | ||||||
| chr3:142750957
|
T | C | 1 | a0001c0002t0001g0041 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.632+2497T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142750957 | ||||||
| chr3:142750991
|
T | C | 1 | a0002c0009t0007g0038 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.632+2531T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142750991 | ||||||
| chr3:142751332
|
C | A | 1 | a0001c0003t0001g0033 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.632+2872C>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142751332 | ||||||
| chr3:142751435
|
G | T | 1 | a0001c0002t0001g0227 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.632+2975G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142751435 | ||||||
| chr3:142751459
|
T | C | 1 | a0001c0002t0001g0041 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.632+2999T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142751459 | ||||||
| chr3:142751529
|
C | A | 42 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0104others(39): Show | 44 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.632+3069C>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142751529 | ||||||
| chr3:142751666
|
C | G | 1 | a0001c0002t0001g0227 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.632+3206C>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142751666 | ||||||
| chr3:142751805
|
A | C | 1 | a0001c0001t0001g0180 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.632+3345A>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142751805 | ||||||
| chr3:142751873
|
A | G | 1 | a0001c0003t0001g0240 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.632+3413A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142751873 | ||||||
| chr3:142751885
|
A | G | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.632+3425A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142751885 | ||||||
| chr3:142751922
|
C | A | 1 | a0001c0001t0001g0187 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.632+3462C>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142751922 | ||||||
| chr3:142751933
|
C | T | 9 | a0001c0001t0001g0157a0001c0001t0008g0138a0001c0001t0008g0139others(6): Show | 9 | HG01243.hp2 HG02145.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.632+3473C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142751933 | ||||||
| chr3:142751967
|
A | T | 1 | a0001c0001t0007g0107 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.632+3507A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142751967 | ||||||
| chr3:142752365
|
G | A | 1 | a0001c0002t0001g0042 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.632+3905G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142752365 | ||||||
| chr3:142752370
|
C | T | 1 | a0001c0001t0002g0133 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.632+3910C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142752370 | ||||||
| chr3:142752374
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.632+3914G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142752374 | ||||||
| chr3:142752493
|
T | C | 1 | a0001c0002t0001g0279 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.632+4033T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142752493 | ||||||
| chr3:142752600
|
T | G | 1 | a0002c0009t0007g0038 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.632+4140T>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142752600 | ||||||
| chr3:142752810
|
C | T | 181 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(178): Show | 203 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.632+4350C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142752810 | ||||||
| chr3:142752844
|
A | C | 181 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(178): Show | 203 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.632+4384A>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142752844 | ||||||
| chr3:142752914
|
C | A | 3 | a0001c0003t0004g0002a0001c0003t0004g0058a0001c0003t0004g0068 | 6 | NA18963.hp1 NA18971.hp2 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.632+4454C>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142752914 | ||||||
| chr3:142752921
|
G | T | 1 | a0001c0001t0001g0079 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.632+4461G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142752921 | ||||||
| chr3:142753094
|
C | T | 42 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0104others(39): Show | 44 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.632+4634C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142753094 | ||||||
| chr3:142753100
|
A | G | 3 | a0001c0003t0006g0237a0001c0003t0006g0238a0001c0003t0006g0250 | 3 | HG02257.hp1 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.632+4640A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142753100 | ||||||
| chr3:142753227
|
T | C | 33 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(30): Show | 36 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.632+4767T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142753227 | ||||||
| chr3:142753360
|
G | C | 17 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(14): Show | 18 | HG00323.hp1 HG00738.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.632+4900G>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142753360 | ||||||
| chr3:142753518
|
C | A | 1 | a0001c0001t0001g0187 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.632+5058C>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142753518 | ||||||
| chr3:142753562
|
C | T | 21 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(18): Show | 23 | HG00323.hp1 HG00738.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.632+5102C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142753562 | ||||||
| chr3:142753625
|
C | T | 20 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(17): Show | 24 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.632+5165C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142753625 | ||||||
| chr3:142753726
|
C | CA | 119 | a0001c0001t0001g0077a0001c0001t0001g0082a0001c0001t0001g0153others(116): Show | 133 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.632+5286dupA | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142753726 | |||||
| chr3:142753726
|
C | CAA | 23 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(20): Show | 24 | HG01361.hp2 HG01496.hp1 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.632+5285_632+5286d others(4): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142753726 | |||||
| chr3:142753726
|
CA | C | 20 | a0001c0001t0008g0156a0001c0003t0001g0023a0001c0003t0004g0002others(17): Show | 24 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.632+5286delA | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142753726 | |||||
| chr3:142753965
|
G | A | 3 | a0001c0004t0005g0017a0001c0004t0005g0019a0001c0004t0005g0278 | 5 | NA18994.hp2 NA18999.hp2 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.632+5505G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142753965 | ||||||
| chr3:142754089
|
C | CA | 9 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0157others(6): Show | 9 | HG00438.hp1 HG01074.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.632+5653dupA | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142754089 | |||||
| chr3:142754089
|
CA | C | 19 | a0001c0001t0001g0099a0001c0001t0001g0179a0001c0001t0001g0186others(16): Show | 20 | HG00099.hp1 HG00621.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.632+5653delA | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142754089 | |||||
| chr3:142754089
|
CAA | C | 56 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0002t0001g0044others(53): Show | 63 | HG00673.hp2 HG00738.hp2 HG01123.hp1 others(60): Show |
intron_variant | MODIFIER | c.632+5652_632+5653d others(4): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142754089 | |||||
| chr3:142754089
|
CAAA | C | 107 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(104): Show | 121 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.632+5651_632+5653d others(5): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142754089 | |||||
| chr3:142754089
|
CAAAA | C | 12 | a0001c0002t0001g0047a0001c0002t0001g0052a0001c0002t0001g0105others(9): Show | 12 | HG00323.hp2 HG01070.hp1 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.632+5650_632+5653d others(6): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142754089 | |||||
| chr3:142754112
|
A | G | 1 | a0001c0002t0001g0225 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.632+5652A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142754112 | ||||||
| chr3:142754265
|
A | G | 1 | a0001c0001t0002g0098 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.632+5805A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142754265 | ||||||
| chr3:142754275
|
A | G | 1 | a0001c0002t0001g0209 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.632+5815A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142754275 | ||||||
| chr3:142754379
|
A | G | 1 | a0001c0001t0003g0286 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.632+5919A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142754379 | ||||||
| chr3:142754740
|
G | A | 2 | a0001c0001t0003g0284a0001c0001t0003g0286 | 2 | HG01496.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.632+6280G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142754740 | ||||||
| chr3:142754809
|
G | A | 4 | a0001c0003t0003g0006a0001c0003t0003g0073a0001c0003t0003g0074others(1): Show | 5 | HG01884.hp1 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.632+6349G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142754809 | ||||||
| chr3:142754928
|
A | G | 151 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(148): Show | 168 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.632+6468A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142754928 | ||||||
| chr3:142755062
|
C | A | 21 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(18): Show | 23 | HG00323.hp1 HG00738.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.632+6602C>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142755062 | ||||||
| chr3:142755072
|
T | C | 1 | a0002c0009t0007g0038 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.632+6612T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142755072 | ||||||
| chr3:142755087
|
T | C | 20 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(17): Show | 24 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.632+6627T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142755087 | ||||||
| chr3:142755282
|
G | A | 3 | a0001c0002t0001g0013a0001c0002t0001g0228a0001c0002t0001g0229 | 4 | NA18995.hp1 NA19056.hp2 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.632+6822G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142755282 | ||||||
| chr3:142755557
|
T | G | 24 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0031others(21): Show | 31 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.632+7097T>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142755557 | ||||||
| chr3:142755608
|
G | A | 1 | a0002c0005t0007g0070 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.632+7148G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142755608 | ||||||
| chr3:142755722
|
A | T | 1 | a0001c0001t0007g0107 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.632+7262A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142755722 | ||||||
| chr3:142755939
|
A | T | 1 | a0001c0001t0002g0108 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.632+7479A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142755939 | ||||||
| chr3:142755961
|
G | T | 20 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(17): Show | 24 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.632+7501G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142755961 | ||||||
| chr3:142756044
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.632+7584A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142756044 | ||||||
| chr3:142756138
|
C | A | 33 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(30): Show | 36 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.632+7678C>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142756138 | ||||||
| chr3:142756156
|
A | G | 1 | a0001c0006t0006g0306 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.632+7696A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142756156 | ||||||
| chr3:142756326
|
C | T | 18 | a0001c0003t0004g0002a0001c0003t0004g0004a0001c0003t0004g0005others(15): Show | 22 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.632+7866C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142756326 | ||||||
| chr3:142756361
|
C | CT | 38 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0031others(35): Show | 46 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.632+7917dupT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142756361 | |||||
| chr3:142756361
|
C | CTT | 18 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(15): Show | 22 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.632+7916_632+7917d others(4): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142756361 | |||||
| chr3:142756383
|
A | G | 151 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(148): Show | 168 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.632+7923A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142756383 | ||||||
| chr3:142756403
|
A | G | 21 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(18): Show | 23 | HG00323.hp1 HG00738.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.632+7943A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142756403 | ||||||
| chr3:142756436
|
T | C | 1 | a0001c0002t0001g0206 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.632+7976T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142756436 | ||||||
| chr3:142756504
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.632+8044C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142756504 | ||||||
| chr3:142756522
|
G | C | 1 | a0001c0001t0001g0097 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.632+8062G>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142756522 | ||||||
| chr3:142756602
|
G | A | 8 | a0001c0001t0008g0138a0001c0001t0008g0139a0001c0001t0008g0140others(5): Show | 8 | HG01243.hp2 HG02145.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.632+8142G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142756602 | ||||||
| chr3:142757152
|
T | A | 1 | a0001c0001t0003g0285 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.632+8692T>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142757152 | ||||||
| chr3:142757206
|
G | T | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.632+8746G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142757206 | ||||||
| chr3:142757230
|
GAT | G | 182 | a0001c0001t0001g0178a0001c0001t0003g0020a0001c0001t0003g0284others(179): Show | 204 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.632+8783_632+8784d others(4): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142757230 | |||||
| chr3:142757291
|
A | T | 14 | a0001c0001t0001g0163a0001c0001t0002g0109a0001c0003t0010g0022others(11): Show | 14 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.632+8831A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142757291 | ||||||
| chr3:142757319
|
A | G | 1 | a0001c0006t0001g0300 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.632+8859A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142757319 | ||||||
| chr3:142757330
|
A | G | 10 | a0002c0005t0007g0026a0002c0005t0007g0027a0002c0005t0007g0028others(7): Show | 10 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.632+8870A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142757330 | ||||||
| chr3:142757335
|
T | C | 1 | a0002c0009t0007g0038 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.632+8875T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142757335 | ||||||
| chr3:142757339
|
A | T | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.632+8879A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142757339 | ||||||
| chr3:142757356
|
C | CAT | 181 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(178): Show | 203 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.632+8897_632+8898d others(4): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142757356 | |||||
| chr3:142757546
|
G | A | 1 | a0001c0008t0009g0024 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.632+9086G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142757546 | ||||||
| chr3:142757590
|
T | C | 1 | a0001c0001t0001g0084 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.632+9130T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142757590 | ||||||
| chr3:142757703
|
T | C | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283 | 3 | HG01496.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.632+9243T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142757703 | ||||||
| chr3:142757824
|
A | T | 1 | a0001c0001t0001g0187 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.632+9364A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142757824 | ||||||
| chr3:142757941
|
G | C | 1 | a0001c0001t0002g0085 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.632+9481G>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142757941 | ||||||
| chr3:142757976
|
ACT | A | 4 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0166others(1): Show | 4 | NA18948.hp1 NA19002.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.632+9519_632+9520d others(4): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142757976 | |||||
| chr3:142758039
|
G | A | 2 | a0001c0008t0009g0024a0001c0008t0009g0025 | 2 | HG01255.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.632+9579G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142758039 | ||||||
| chr3:142758155
|
G | C | 1 | a0001c0001t0003g0284 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.632+9695G>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142758155 | ||||||
| chr3:142758300
|
A | T | 42 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0104others(39): Show | 44 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.632+9840A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142758300 | ||||||
| chr3:142758325
|
A | G | 18 | a0001c0004t0005g0017a0001c0004t0005g0018a0001c0004t0005g0019others(15): Show | 21 | HG00673.hp2 HG00738.hp2 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.632+9865A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142758325 | ||||||
| chr3:142758556
|
G | A | 2 | a0001c0008t0009g0024a0001c0008t0009g0025 | 2 | HG01255.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.632+10096G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142758556 | ||||||
| chr3:142758668
|
T | C | 1 | a0001c0002t0001g0045 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.632+10208T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142758668 | ||||||
| chr3:142758896
|
A | G | 3 | a0001c0002t0001g0104a0001c0002t0001g0105a0001c0002t0001g0232 | 3 | NA18953.hp1 NA18998.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.632+10436A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142758896 | ||||||
| chr3:142759023
|
G | A | 1 | a0001c0001t0002g0111 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.632+10563G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142759023 | ||||||
| chr3:142759058
|
T | C | 154 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(151): Show | 174 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.632+10598T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142759058 | ||||||
| chr3:142759071
|
A | G | 1 | a0001c0001t0003g0285 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.632+10611A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142759071 | ||||||
| chr3:142759072
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.632+10612T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142759072 | ||||||
| chr3:142759098
|
C | T | 2 | a0001c0008t0009g0024a0001c0008t0009g0025 | 2 | HG01255.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.632+10638C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142759098 | ||||||
| chr3:142759270
|
G | A | 134 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(131): Show | 150 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.632+10810G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142759270 | ||||||
| chr3:142759666
|
T | C | 31 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(28): Show | 34 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.632+11206T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142759666 | ||||||
| chr3:142759667
|
G | A | 14 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(11): Show | 15 | HG00735.hp2 HG01109.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.632+11207G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142759667 | ||||||
| chr3:142759667
|
G | C | 1 | a0001c0001t0008g0143 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.632+11207G>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142759667 | ||||||
| chr3:142759724
|
G | A | 1 | a0001c0003t0006g0255 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.632+11264G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142759724 | ||||||
| chr3:142759836
|
TA | T | 8 | a0001c0001t0002g0009a0001c0001t0002g0109a0001c0001t0002g0125others(5): Show | 9 | NA18939.hp2 NA18948.hp2 NA18957.hp1 others(6): Show |
intron_variant | MODIFIER | c.632+11379delA | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142759836 | |||||
| chr3:142759867
|
G | A | 20 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(17): Show | 24 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.632+11407G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142759867 | ||||||
| chr3:142759916
|
G | A | 2 | a0001c0001t0003g0293a0001c0001t0003g0298 | 2 | HG01169.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.632+11456G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142759916 | ||||||
| chr3:142759918
|
G | A | 2 | a0001c0002t0001g0211a0001c0002t0001g0212 | 2 | HG02273.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.632+11458G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142759918 | ||||||
| chr3:142759941
|
G | A | 1 | a0001c0004t0005g0265 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.632+11481G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142759941 | ||||||
| chr3:142760077
|
C | T | 20 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(17): Show | 24 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.632+11617C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142760077 | ||||||
| chr3:142760165
|
G | T | 164 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(161): Show | 185 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.632+11705G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142760165 | ||||||
| chr3:142760240
|
G | T | 134 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(131): Show | 150 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.632+11780G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142760240 | ||||||
| chr3:142760280
|
T | A | 42 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0104others(39): Show | 44 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.632+11820T>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142760280 | ||||||
| chr3:142760332
|
A | G | 5 | a0001c0004t0005g0267a0001c0004t0005g0268a0001c0004t0005g0273others(2): Show | 5 | NA18985.hp1 NA19012.hp2 NA19083.hp2 others(2): Show |
intron_variant | MODIFIER | c.632+11872A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142760332 | ||||||
| chr3:142761202
|
G | C | 1 | a0001c0002t0001g0209 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.632+12742G>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142761202 | ||||||
| chr3:142761374
|
A | G | 1 | a0001c0002t0001g0199 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.632+12914A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142761374 | ||||||
| chr3:142761424
|
T | C | 18 | a0001c0003t0004g0002a0001c0003t0004g0004a0001c0003t0004g0005others(15): Show | 22 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.632+12964T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142761424 | ||||||
| chr3:142761549
|
C | CGGGGGGT others(10): Show |
1 | a0001c0003t0004g0057 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.632+13089_632+1309 others(21): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142761549 | ||||||
| chr3:142761703
|
G | T | 134 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(131): Show | 150 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.632+13243G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142761703 | ||||||
| chr3:142761707
|
AC | A | 33 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(30): Show | 36 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.632+13248delC | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142761707 | ||||||
| chr3:142761741
|
G | A | 4 | a0001c0003t0003g0006a0001c0003t0003g0073a0001c0003t0003g0074others(1): Show | 5 | HG01884.hp1 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.632+13281G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142761741 | ||||||
| chr3:142761934
|
T | A | 144 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(141): Show | 161 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.632+13474T>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142761934 | ||||||
| chr3:142762023
|
G | A | 33 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(30): Show | 36 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.632+13563G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142762023 | ||||||
| chr3:142762113
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.632+13653G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142762113 | ||||||
| chr3:142762143
|
C | G | 1 | a0001c0001t0001g0165 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.632+13683C>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142762143 | ||||||
| chr3:142762317
|
T | C | 22 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0031others(19): Show | 29 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.632+13857T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142762317 | ||||||
| chr3:142762341
|
T | C | 1 | a0001c0003t0001g0261 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.632+13881T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142762341 | ||||||
| chr3:142762410
|
C | G | 144 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(141): Show | 161 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.632+13950C>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142762410 | ||||||
| chr3:142762428
|
A | AT | 17 | a0001c0001t0001g0072a0001c0001t0001g0096a0001c0001t0001g0166others(14): Show | 18 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.632+13989dupT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142762428 | |||||
| chr3:142762428
|
A | ATT | 18 | a0001c0002t0001g0201a0001c0002t0001g0223a0001c0004t0005g0017others(15): Show | 21 | HG00323.hp2 HG00738.hp2 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.632+13988_632+1398 others(6): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142762428 | |||||
| chr3:142762428
|
A | ATTT | 40 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0104others(37): Show | 42 | HG00423.hp1 HG00597.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.632+13987_632+1398 others(7): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142762428 | |||||
| chr3:142762428
|
A | ATTTT | 9 | a0001c0002t0001g0207a0001c0002t0001g0210a0001c0002t0001g0212others(6): Show | 10 | HG01884.hp1 HG01934.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.632+13986_632+1398 others(8): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142762428 | |||||
| chr3:142762428
|
AT | A | 24 | a0001c0001t0001g0170a0001c0001t0001g0187a0001c0001t0002g0131others(21): Show | 28 | HG00621.hp1 HG01074.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.632+13989delT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142762428 | |||||
| chr3:142762453
|
G | A | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.632+13993G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142762453 | ||||||
| chr3:142762511
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.632+14051C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142762511 | ||||||
| chr3:142762521
|
C | T | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283 | 3 | HG01496.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.632+14061C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142762521 | ||||||
| chr3:142762620
|
G | T | 1 | a0001c0003t0004g0057 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.632+14160G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142762620 | ||||||
| chr3:142762662
|
C | A | 1 | a0001c0002t0001g0045 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.632+14202C>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142762662 | ||||||
| chr3:142762679
|
G | A | 1 | a0001c0003t0001g0023 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.632+14219G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142762679 | ||||||
| chr3:142762718
|
C | T | 3 | a0001c0002t0001g0042a0001c0002t0001g0049a0001c0002t0001g0052 | 3 | HG00544.hp1 NA18950.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.632+14258C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142762718 | ||||||
| chr3:142762752
|
A | C | 130 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(127): Show | 145 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.632+14292A>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142762752 | ||||||
| chr3:142762801
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.632+14341A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142762801 | ||||||
| chr3:142763196
|
G | A | 3 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0051 | 3 | HG01070.hp1 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.633-14436G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142763196 | ||||||
| chr3:142763235
|
A | G | 1 | a0001c0001t0001g0166 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.633-14397A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142763235 | ||||||
| chr3:142763255
|
G | C | 1 | a0001c0003t0011g0251 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.633-14377G>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142763255 | ||||||
| chr3:142763409
|
G | T | 134 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(131): Show | 150 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.633-14223G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142763409 | ||||||
| chr3:142763451
|
C | T | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283 | 3 | HG01496.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.633-14181C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142763451 | ||||||
| chr3:142763495
|
A | T | 144 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(141): Show | 161 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.633-14137A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142763495 | ||||||
| chr3:142763631
|
C | T | 33 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(30): Show | 36 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.633-14001C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142763631 | ||||||
| chr3:142763753
|
C | T | 1 | a0001c0002t0001g0220 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.633-13879C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142763753 | ||||||
| chr3:142763904
|
A | T | 4 | a0001c0004t0005g0018a0001c0004t0005g0264a0001c0004t0005g0266others(1): Show | 5 | HG00673.hp2 NA18612.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.633-13728A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142763904 | ||||||
| chr3:142763935
|
C | G | 1 | a0001c0001t0001g0164 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.633-13697C>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142763935 | ||||||
| chr3:142763959
|
A | AAT | 13 | a0001c0001t0001g0165a0001c0001t0001g0169a0001c0001t0001g0176others(10): Show | 14 | HG00408.hp2 HG00544.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.633-13649_633-1364 others(6): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763959 | |||||
| chr3:142763959
|
A | AATATATA others(3): Show |
6 | a0001c0001t0008g0138a0001c0001t0008g0140a0001c0001t0008g0143others(3): Show | 6 | HG02145.hp2 HG02895.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.633-13657_633-1364 others(14): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763959 | |||||
| chr3:142763959
|
A | AATATATA others(7): Show |
3 | a0001c0001t0001g0082a0001c0001t0001g0106a0001c0001t0007g0107 | 3 | HG02976.hp2 NA19066.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.633-13661_633-1364 others(18): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763959 | |||||
| chr3:142763959
|
A | AATATATA others(9): Show |
7 | a0001c0001t0001g0007a0001c0001t0001g0071a0001c0001t0001g0072others(4): Show | 8 | HG00438.hp2 HG00642.hp2 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.633-13663_633-1364 others(20): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763959 | |||||
| chr3:142763959
|
A | AATATATA others(11): Show |
15 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0095others(12): Show | 16 | HG00735.hp1 HG01081.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.633-13665_633-1364 others(22): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763959 | |||||
| chr3:142763959
|
A | AATATATA others(13): Show |
29 | a0001c0001t0001g0079a0001c0001t0001g0091a0001c0001t0001g0092others(26): Show | 30 | HG00597.hp1 HG00609.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.633-13667_633-1364 others(24): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763959 | |||||
| chr3:142763959
|
A | AATATATA others(15): Show |
11 | a0001c0001t0001g0120a0001c0001t0002g0010a0001c0001t0002g0076others(8): Show | 12 | HG01070.hp2 HG01255.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.633-13669_633-1364 others(26): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763959 | |||||
| chr3:142763959
|
A | AATATATA others(17): Show |
6 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0002g0127others(3): Show | 6 | HG00738.hp1 HG03017.hp2 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.633-13671_633-1364 others(28): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763959 | |||||
| chr3:142763959
|
A | AATATATA others(19): Show |
1 | a0001c0001t0002g0129 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.633-13648_633-1364 others(30): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763959 | |||||
| chr3:142763959
|
A | AATATATA others(21): Show |
2 | a0001c0001t0002g0134a0001c0001t0002g0137 | 2 | HG04204.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.633-13648_633-1364 others(32): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763959 | |||||
| chr3:142763959
|
A | AATATATA others(25): Show |
1 | a0001c0001t0001g0281 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.633-13648_633-1364 others(36): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763959 | |||||
| chr3:142763959
|
A | ATATATAT others(12): Show |
2 | a0001c0001t0002g0122a0001c0001t0002g0132 | 2 | HG02735.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.633-13673_633-1367 others(23): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142763959 | ||||||
| chr3:142763959
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0002g0123 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.633-13673_633-1367 others(25): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142763959 | ||||||
| chr3:142763959
|
A | T | 1 | a0001c0001t0003g0290 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.633-13673A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142763959 | ||||||
| chr3:142763959
|
AATATATA others(35): Show |
A | 19 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(16): Show | 23 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.633-13657_633-1361 others(46): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763959 | |||||
| chr3:142763959
|
AATATATA others(37): Show |
A | 1 | a0001c0003t0004g0057 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.633-13659_633-1361 others(48): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763959 | |||||
| chr3:142763961
|
TATATATA others(31): Show |
T | 96 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(93): Show | 108 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.633-13653_633-1361 others(42): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763961 | |||||
| chr3:142763963
|
TATATATA others(29): Show |
T | 1 | a0001c0002t0001g0231 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.633-13651_633-1361 others(40): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763963 | |||||
| chr3:142763967
|
TATATATA others(25): Show |
T | 4 | a0001c0003t0001g0258a0001c0003t0001g0259a0001c0003t0001g0260others(1): Show | 4 | HG02486.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.633-13647_633-1361 others(36): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763967 | |||||
| chr3:142763969
|
TATATATA others(23): Show |
T | 1 | a0001c0003t0001g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.633-13647_633-1361 others(34): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763969 | |||||
| chr3:142763975
|
TATATATA others(17): Show |
T | 2 | a0001c0003t0006g0015a0001c0003t0006g0247 | 3 | HG02280.hp1 HG03130.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.633-13647_633-1362 others(28): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763975 | |||||
| chr3:142763977
|
TATATATA others(15): Show |
T | 7 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0302others(4): Show | 8 | HG02280.hp2 HG02486.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.633-13647_633-1362 others(26): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763977 | |||||
| chr3:142763977
|
TATATATA others(33): Show |
T | 1 | a0001c0003t0006g0014 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.633-13654_633-1361 others(44): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142763977 | ||||||
| chr3:142763979
|
TATATACA others(13): Show |
T | 1 | a0001c0006t0001g0304 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.633-13647_633-1362 others(24): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763979 | |||||
| chr3:142763979
|
TATATACA others(31): Show |
T | 1 | a0001c0003t0001g0280 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.633-13652_633-1361 others(42): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142763979 | ||||||
| chr3:142763981
|
T | TATATATA others(19): Show |
1 | a0001c0001t0003g0289 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.633-13648_633-1364 others(30): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763981 | |||||
| chr3:142763981
|
T | TATATATA others(21): Show |
1 | a0001c0001t0002g0121 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.633-13648_633-1364 others(32): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763981 | |||||
| chr3:142763981
|
TATACACA others(3): Show |
T | 3 | a0001c0003t0001g0016a0001c0003t0001g0242a0001c0006t0001g0301 | 4 | HG02895.hp1 HG02897.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.633-13645_633-1363 others(14): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763981 | |||||
| chr3:142763981
|
TATACACA others(7): Show |
T | 4 | a0001c0003t0003g0075a0001c0003t0006g0246a0001c0003t0006g0249others(1): Show | 4 | HG02559.hp1 HG02970.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.633-13645_633-1363 others(18): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763981 | |||||
| chr3:142763981
|
TATACACA others(11): Show |
T | 3 | a0001c0003t0001g0252a0001c0003t0003g0073a0001c0006t0001g0305 | 3 | HG01884.hp1 HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.633-13647_633-1363 others(22): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763981 | |||||
| chr3:142763983
|
T | TATATATA others(13): Show |
1 | a0001c0001t0002g0098 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.633-13648_633-1364 others(24): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763983 | |||||
| chr3:142763983
|
T | TATATATA others(15): Show |
1 | a0001c0001t0002g0142 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.633-13648_633-1364 others(26): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763983 | |||||
| chr3:142763983
|
T | TATATATA others(19): Show |
2 | a0001c0001t0002g0116a0001c0001t0002g0117 | 2 | HG01169.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.633-13648_633-1364 others(30): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763983 | |||||
| chr3:142763983
|
T | TATATATA others(21): Show |
1 | a0001c0001t0002g0124 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.633-13648_633-1364 others(32): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763983 | |||||
| chr3:142763983
|
T | TATATATA others(27): Show |
1 | a0001c0001t0002g0133 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.633-13648_633-1364 others(38): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763983 | |||||
| chr3:142763983
|
TACACATA others(1): Show |
T | 7 | a0001c0003t0003g0006a0001c0003t0003g0074a0001c0003t0006g0239others(4): Show | 8 | HG02615.hp1 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.633-13647_633-1364 others(12): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763983 | |||||
| chr3:142763983
|
TACACATA others(5): Show |
T | 7 | a0001c0003t0001g0240a0001c0003t0001g0262a0001c0003t0006g0238others(4): Show | 7 | HG00642.hp1 HG01175.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.633-13647_633-1363 others(16): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763983 | |||||
| chr3:142763983
|
TACACATA others(9): Show |
T | 1 | a0001c0003t0006g0237 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.633-13647_633-1363 others(20): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763983 | |||||
| chr3:142763985
|
C | T | 5 | a0001c0001t0001g0077a0001c0001t0001g0281a0001c0001t0001g0282others(2): Show | 5 | HG01433.hp2 HG01496.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.633-13647C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142763985 | ||||||
| chr3:142763987
|
C | T | 5 | a0001c0001t0001g0077a0001c0001t0001g0281a0001c0001t0001g0282others(2): Show | 5 | HG01433.hp2 HG01496.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.633-13645C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142763987 | ||||||
| chr3:142763989
|
T | TATATATA others(7): Show |
1 | a0001c0001t0001g0077 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.633-13642_633-1364 others(18): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763989 | |||||
| chr3:142763991
|
C | T | 5 | a0001c0003t0001g0254a0001c0003t0001g0263a0001c0003t0006g0241others(2): Show | 5 | HG00735.hp2 HG01255.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.633-13641C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142763991 | ||||||
| chr3:142763995
|
C | T | 15 | a0001c0003t0001g0016a0001c0003t0001g0242a0001c0003t0001g0254others(12): Show | 17 | HG00735.hp2 HG01255.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.633-13637C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142763995 | ||||||
| chr3:142763999
|
C | T | 26 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(23): Show | 28 | HG00642.hp1 HG00735.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.633-13633C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142763999 | ||||||
| chr3:142763999
|
CAT | C | 7 | a0001c0001t0008g0138a0001c0001t0008g0139a0001c0001t0008g0140others(4): Show | 7 | HG02145.hp2 HG02723.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.633-13617_633-1361 others(6): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142763999 | |||||
| chr3:142764017
|
A | T | 31 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(28): Show | 33 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.633-13615A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142764017 | ||||||
| chr3:142764079
|
CA | C | 134 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(131): Show | 150 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.633-13544delA | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142764079 | |||||
| chr3:142764114
|
ACATTTTC others(41): Show |
A | 1 | a0001c0001t0002g0142 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.633-13468_633-1342 others(52): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142764114 | |||||
| chr3:142764184
|
A | G | 35 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0031others(32): Show | 42 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.633-13448A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142764184 | ||||||
| chr3:142764188
|
A | G | 144 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(141): Show | 161 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.633-13444A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142764188 | ||||||
| chr3:142764274
|
G | A | 33 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(30): Show | 36 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.633-13358G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142764274 | ||||||
| chr3:142764357
|
T | C | 134 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(131): Show | 150 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.633-13275T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142764357 | ||||||
| chr3:142764443
|
A | G | 273 | a0001c0001t0001g0007a0001c0001t0001g0071a0001c0001t0001g0072others(270): Show | 299 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(296): Show |
intron_variant | MODIFIER | c.633-13189A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142764443 | ||||||
| chr3:142764552
|
G | C | 1 | a0001c0003t0004g0057 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.633-13080G>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142764552 | ||||||
| chr3:142764553
|
C | T | 1 | a0001c0003t0004g0057 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.633-13079C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142764553 | ||||||
| chr3:142764554
|
T | G | 19 | a0001c0002t0001g0279a0001c0004t0005g0017a0001c0004t0005g0018others(16): Show | 22 | HG00673.hp2 HG00738.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.633-13078T>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142764554 | ||||||
| chr3:142764876
|
A | G | 35 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0031others(32): Show | 42 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.633-12756A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142764876 | ||||||
| chr3:142764932
|
G | A | 33 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(30): Show | 36 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.633-12700G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142764932 | ||||||
| chr3:142765146
|
C | G | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.633-12486C>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142765146 | ||||||
| chr3:142765481
|
C | T | 1 | a0001c0006t0001g0305 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.633-12151C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142765481 | ||||||
| chr3:142765482
|
G | A | 1 | a0001c0003t0004g0059 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.633-12150G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142765482 | ||||||
| chr3:142765499
|
A | C | 1 | a0001c0001t0002g0094 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.633-12133A>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142765499 | ||||||
| chr3:142765787
|
G | A | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.633-11845G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142765787 | ||||||
| chr3:142765822
|
G | A | 134 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(131): Show | 150 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.633-11810G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142765822 | ||||||
| chr3:142765932
|
C | A | 20 | a0001c0002t0001g0279a0001c0004t0005g0017a0001c0004t0005g0018others(17): Show | 23 | HG00673.hp2 HG00738.hp2 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.633-11700C>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142765932 | ||||||
| chr3:142766078
|
A | G | 134 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(131): Show | 150 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.633-11554A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142766078 | ||||||
| chr3:142766081
|
G | A | 1 | a0001c0003t0006g0253 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.633-11551G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142766081 | ||||||
| chr3:142766409
|
CT | C | 19 | a0001c0004t0005g0017a0001c0004t0005g0018a0001c0004t0005g0019others(16): Show | 22 | HG00673.hp2 HG00738.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.633-11214delT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142766409 | |||||
| chr3:142766464
|
G | T | 4 | a0001c0003t0003g0006a0001c0003t0003g0073a0001c0003t0003g0074others(1): Show | 5 | HG01884.hp1 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.633-11168G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142766464 | ||||||
| chr3:142766496
|
G | A | 20 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(17): Show | 24 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.633-11136G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142766496 | ||||||
| chr3:142766589
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.633-11043C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142766589 | ||||||
| chr3:142766616
|
G | A | 1 | a0001c0002t0001g0213 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.633-11016G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142766616 | ||||||
| chr3:142766786
|
C | T | 2 | a0001c0008t0009g0024a0001c0008t0009g0025 | 2 | HG01255.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.633-10846C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142766786 | ||||||
| chr3:142766794
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.633-10838G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142766794 | ||||||
| chr3:142766897
|
C | T | 4 | a0001c0006t0001g0303a0001c0006t0001g0304a0001c0006t0001g0305others(1): Show | 4 | HG02280.hp2 HG02451.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.633-10735C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142766897 | ||||||
| chr3:142767143
|
C | G | 1 | a0001c0001t0001g0077 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.633-10489C>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142767143 | ||||||
| chr3:142767434
|
G | T | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.633-10198G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142767434 | ||||||
| chr3:142767456
|
T | C | 20 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(17): Show | 24 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.633-10176T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142767456 | ||||||
| chr3:142767490
|
C | CT | 33 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(30): Show | 36 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.633-10135dupT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142767490 | |||||
| chr3:142767618
|
A | G | 2 | a0001c0003t0003g0073a0001c0003t0003g0075 | 2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.633-10014A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142767618 | ||||||
| chr3:142767622
|
T | G | 1 | a0001c0001t0002g0309 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.633-10010T>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142767622 | ||||||
| chr3:142767911
|
GT | G | 165 | a0001c0001t0008g0143a0001c0002t0001g0001a0001c0002t0001g0003others(162): Show | 186 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.633-9711delT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142767911 | |||||
| chr3:142768058
|
G | A | 164 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(161): Show | 185 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.633-9574G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142768058 | ||||||
| chr3:142768136
|
A | G | 2 | a0001c0002t0001g0047a0001c0003t0006g0015 | 3 | HG01070.hp1 HG02280.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.633-9496A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142768136 | ||||||
| chr3:142768556
|
G | A | 3 | a0001c0003t0006g0239a0001c0003t0006g0248a0001c0003t0006g0255 | 3 | HG00642.hp1 HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.633-9076G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142768556 | ||||||
| chr3:142768649
|
C | T | 168 | a0001c0001t0001g0077a0001c0001t0001g0281a0001c0001t0001g0282others(165): Show | 189 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.633-8983C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142768649 | ||||||
| chr3:142768724
|
G | GT | 20 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(17): Show | 24 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.633-8902dupT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142768724 | |||||
| chr3:142768923
|
T | C | 164 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(161): Show | 185 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.633-8709T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142768923 | ||||||
| chr3:142769079
|
A | G | 20 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(17): Show | 24 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.633-8553A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142769079 | ||||||
| chr3:142769231
|
TCAC | T | 8 | a0001c0001t0001g0146a0001c0001t0008g0138a0001c0001t0008g0139others(5): Show | 8 | HG01243.hp1 HG02145.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.633-8397_633-8395d others(5): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142769231 | |||||
| chr3:142769339
|
ATCTT | A | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.633-8288_633-8285d others(6): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142769339 | |||||
| chr3:142769400
|
G | A | 33 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(30): Show | 36 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.633-8232G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142769400 | ||||||
| chr3:142769683
|
T | A | 1 | a0001c0002t0001g0032 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.633-7949T>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142769683 | ||||||
| chr3:142769958
|
A | G | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283 | 3 | HG01496.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.633-7674A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142769958 | ||||||
| chr3:142770093
|
C | CT | 100 | a0001c0001t0001g0077a0001c0001t0001g0153a0001c0001t0001g0281others(97): Show | 115 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.633-7517dupT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142770093 | |||||
| chr3:142770093
|
C | CTT | 12 | a0001c0002t0001g0003a0001c0002t0001g0050a0001c0002t0001g0053others(9): Show | 13 | HG00408.hp1 HG02055.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.633-7518_633-7517d others(4): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142770093 | |||||
| chr3:142770093
|
CT | C | 8 | a0001c0001t0001g0178a0001c0001t0002g0090a0001c0001t0015g0155others(5): Show | 9 | HG01081.hp1 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.633-7517delT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142770093 | |||||
| chr3:142770142
|
G | A | 134 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(131): Show | 150 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.633-7490G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142770142 | ||||||
| chr3:142770340
|
G | A | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283 | 3 | HG01496.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.633-7292G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142770340 | ||||||
| chr3:142770343
|
C | T | 3 | a0001c0003t0003g0073a0001c0003t0003g0075a0001c0003t0006g0255 | 3 | HG01884.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.633-7289C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142770343 | ||||||
| chr3:142770592
|
C | T | 33 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(30): Show | 36 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.633-7040C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142770592 | ||||||
| chr3:142770621
|
A | C | 1 | a0001c0003t0001g0280 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.633-7011A>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142770621 | ||||||
| chr3:142770729
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.633-6903T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142770729 | ||||||
| chr3:142770865
|
A | G | 1 | a0001c0002t0001g0220 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.633-6767A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142770865 | ||||||
| chr3:142770883
|
G | A | 1 | a0001c0002t0001g0233 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.633-6749G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142770883 | ||||||
| chr3:142771011
|
A | T | 1 | a0001c0002t0001g0031 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.633-6621A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142771011 | ||||||
| chr3:142771085
|
C | A | 1 | a0001c0003t0006g0256 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.633-6547C>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142771085 | ||||||
| chr3:142771309
|
T | C | 164 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(161): Show | 185 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.633-6323T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142771309 | ||||||
| chr3:142771417
|
C | T | 1 | a0001c0004t0005g0278 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.633-6215C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142771417 | ||||||
| chr3:142771523
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.633-6109C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142771523 | ||||||
| chr3:142771584
|
A | C | 42 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0104others(39): Show | 44 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.633-6048A>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142771584 | ||||||
| chr3:142771600
|
A | G | 134 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(131): Show | 150 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.633-6032A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142771600 | ||||||
| chr3:142771912
|
T | C | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0015g0155 | 3 | HG01081.hp1 HG01358.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.633-5720T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142771912 | ||||||
| chr3:142772090
|
G | A | 164 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(161): Show | 185 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.633-5542G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142772090 | ||||||
| chr3:142772324
|
T | C | 20 | a0001c0002t0001g0279a0001c0004t0005g0017a0001c0004t0005g0018others(17): Show | 23 | HG00673.hp2 HG00738.hp2 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.633-5308T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142772324 | ||||||
| chr3:142772333
|
C | G | 4 | a0001c0003t0003g0006a0001c0003t0003g0073a0001c0003t0003g0074others(1): Show | 5 | HG01884.hp1 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.633-5299C>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142772333 | ||||||
| chr3:142772409
|
C | T | 20 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(17): Show | 24 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.633-5223C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142772409 | ||||||
| chr3:142772660
|
AC | A | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.633-4970delC | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142772660 | |||||
| chr3:142772701
|
C | T | 134 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(131): Show | 150 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.633-4931C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142772701 | ||||||
| chr3:142772702
|
G | A | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.633-4930G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142772702 | ||||||
| chr3:142772868
|
A | G | 3 | a0001c0003t0001g0254a0001c0003t0001g0262a0001c0003t0001g0263 | 3 | HG00735.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.633-4764A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142772868 | ||||||
| chr3:142772883
|
C | T | 168 | a0001c0001t0001g0077a0001c0001t0001g0281a0001c0001t0001g0282others(165): Show | 189 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.633-4749C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142772883 | ||||||
| chr3:142773114
|
T | A | 42 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0104others(39): Show | 44 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.633-4518T>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142773114 | ||||||
| chr3:142773141
|
A | G | 18 | a0001c0003t0004g0002a0001c0003t0004g0004a0001c0003t0004g0005others(15): Show | 22 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.633-4491A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142773141 | ||||||
| chr3:142773151
|
T | C | 1 | a0001c0002t0001g0215 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.633-4481T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142773151 | ||||||
| chr3:142773244
|
G | A | 1 | a0001c0002t0001g0311 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.633-4388G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142773244 | ||||||
| chr3:142773298
|
C | T | 1 | a0001c0001t0001g0195 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.633-4334C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142773298 | ||||||
| chr3:142773503
|
A | G | 1 | a0001c0003t0006g0245 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.633-4129A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142773503 | ||||||
| chr3:142773581
|
G | GT | 8 | a0001c0001t0001g0175a0001c0001t0001g0195a0001c0001t0002g0102others(5): Show | 8 | HG01978.hp1 HG01978.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.633-4036dupT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142773581 | |||||
| chr3:142773581
|
GT | G | 42 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(39): Show | 45 | HG00597.hp1 HG00642.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.633-4036delT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142773581 | |||||
| chr3:142773798
|
C | T | 33 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(30): Show | 36 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.633-3834C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142773798 | ||||||
| chr3:142773801
|
C | T | 20 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(17): Show | 24 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.633-3831C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142773801 | ||||||
| chr3:142773984
|
A | T | 2 | a0001c0001t0001g0185a0001c0001t0001g0196 | 2 | HG01261.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.633-3648A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142773984 | ||||||
| chr3:142774057
|
G | A | 1 | a0001c0002t0001g0279 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.633-3575G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142774057 | ||||||
| chr3:142774244
|
A | G | 1 | a0001c0001t0008g0140 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.633-3388A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142774244 | ||||||
| chr3:142774256
|
T | C | 1 | a0002c0005t0007g0055 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.633-3376T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142774256 | ||||||
| chr3:142774464
|
C | A | 1 | a0001c0001t0002g0109 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.633-3168C>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142774464 | ||||||
| chr3:142774587
|
G | C | 4 | a0001c0003t0003g0006a0001c0003t0003g0073a0001c0003t0003g0074others(1): Show | 5 | HG01884.hp1 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.633-3045G>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142774587 | ||||||
| chr3:142774606
|
T | C | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.633-3026T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142774606 | ||||||
| chr3:142774614
|
T | C | 33 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(30): Show | 36 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.633-3018T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142774614 | ||||||
| chr3:142774712
|
TG | T | 20 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(17): Show | 24 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.633-2919delG | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142774712 | ||||||
| chr3:142774715
|
A | AT | 11 | a0001c0002t0001g0043a0001c0006t0001g0021a0001c0006t0001g0300others(8): Show | 12 | HG02040.hp1 HG02280.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.633-2907dupT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142774715 | |||||
| chr3:142774727
|
T | C | 1 | a0001c0003t0006g0246 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.633-2905T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142774727 | ||||||
| chr3:142774824
|
C | T | 42 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0104others(39): Show | 44 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.633-2808C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142774824 | ||||||
| chr3:142774993
|
C | G | 1 | a0001c0003t0001g0280 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.633-2639C>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142774993 | ||||||
| chr3:142775097
|
G | A | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.633-2535G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142775097 | ||||||
| chr3:142775098
|
TATAGGTA others(1): Show |
T | 4 | a0001c0001t0002g0119a0001c0001t0002g0131a0001c0001t0002g0132others(1): Show | 4 | HG01243.hp2 HG01255.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.633-2530_633-2523d others(10): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr3 | 142775098 | |||||
| chr3:142775129
|
T | C | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.633-2503T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142775129 | ||||||
| chr3:142775279
|
T | C | 3 | a0001c0003t0001g0258a0001c0003t0001g0259a0001c0003t0001g0260 | 3 | HG02486.hp2 HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.633-2353T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142775279 | ||||||
| chr3:142775388
|
G | T | 1 | a0001c0001t0003g0296 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.633-2244G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142775388 | ||||||
| chr3:142775491
|
C | T | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.633-2141C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142775491 | ||||||
| chr3:142775532
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.633-2100T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142775532 | ||||||
| chr3:142775888
|
A | T | 164 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(161): Show | 185 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.633-1744A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142775888 | ||||||
| chr3:142776263
|
G | A | 1 | a0002c0005t0007g0037 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.633-1369G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142776263 | ||||||
| chr3:142776264
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.633-1368T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142776264 | ||||||
| chr3:142776582
|
A | C | 167 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(164): Show | 188 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.633-1050A>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142776582 | ||||||
| chr3:142776632
|
C | T | 1 | a0001c0004t0005g0265 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.633-1000C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142776632 | ||||||
| chr3:142776763
|
C | T | 18 | a0001c0003t0004g0002a0001c0003t0004g0004a0001c0003t0004g0005others(15): Show | 22 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.633-869C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142776763 | ||||||
| chr3:142776843
|
C | T | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.633-789C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142776843 | ||||||
| chr3:142777031
|
A | T | 3 | a0001c0001t0002g0121a0001c0001t0002g0122a0001c0001t0002g0130 | 3 | HG02257.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.633-601A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142777031 | ||||||
| chr3:142777124
|
C | T | 4 | a0001c0002t0001g0199a0001c0002t0001g0201a0001c0002t0001g0202others(1): Show | 4 | NA18747.hp1 NA18989.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.633-508C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142777124 | ||||||
| chr3:142777340
|
T | C | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283 | 3 | HG01496.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.633-292T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142777340 | ||||||
| chr3:142777373
|
C | T | 2 | a0001c0001t0001g0174a0001c0001t0001g0178 | 2 | NA18961.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.633-259C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142777373 | ||||||
| chr3:142777578
|
C | T | 1 | a0001c0001t0008g0140 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.633-54C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 4/12 | chr3 | 142777578 | ||||||
| chr3:142777884
|
G | A | 8 | a0001c0001t0001g0146a0001c0001t0008g0138a0001c0001t0008g0139others(5): Show | 8 | HG01243.hp1 HG02145.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.764+121G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 5/12 | chr3 | 142777884 | ||||||
| chr3:142777923
|
G | A | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283 | 3 | HG01496.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.764+160G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 5/12 | chr3 | 142777923 | ||||||
| chr3:142778090
|
G | T | 1 | a0001c0002t0001g0201 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.764+327G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 5/12 | chr3 | 142778090 | ||||||
| chr3:142778109
|
T | C | 18 | a0001c0003t0004g0002a0001c0003t0004g0004a0001c0003t0004g0005others(15): Show | 22 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.764+346T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 5/12 | chr3 | 142778109 | ||||||
| chr3:142778171
|
A | C | 1 | a0001c0001t0003g0292 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.764+408A>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 5/12 | chr3 | 142778171 | ||||||
| chr3:142778462
|
T | C | 1 | a0001c0001t0001g0103 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.764+699T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 5/12 | chr3 | 142778462 | ||||||
| chr3:142778616
|
A | G | 1 | a0001c0003t0001g0023 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.764+853A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 5/12 | chr3 | 142778616 | ||||||
| chr3:142778741
|
C | T | 1 | a0001c0001t0001g0190 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.764+978C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 5/12 | chr3 | 142778741 | ||||||
| chr3:142778808
|
T | G | 1 | a0001c0001t0001g0077 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.764+1045T>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 5/12 | chr3 | 142778808 | ||||||
| chr3:142778810
|
A | T | 1 | a0001c0001t0001g0077 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.764+1047A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 5/12 | chr3 | 142778810 | ||||||
| chr3:142778811
|
T | G | 1 | a0001c0001t0001g0077 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.764+1048T>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 5/12 | chr3 | 142778811 | ||||||
| chr3:142778815
|
C | A | 1 | a0001c0001t0001g0077 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.764+1052C>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 5/12 | chr3 | 142778815 | ||||||
| chr3:142779165
|
G | A | 5 | a0001c0003t0006g0239a0001c0003t0006g0243a0001c0003t0006g0248others(2): Show | 5 | HG00642.hp1 HG01175.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.764+1402G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 5/12 | chr3 | 142779165 | ||||||
| chr3:142779209
|
G | A | 4 | a0001c0006t0001g0303a0001c0006t0001g0304a0001c0006t0001g0305others(1): Show | 4 | HG02280.hp2 HG02451.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.764+1446G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 5/12 | chr3 | 142779209 | ||||||
| chr3:142779539
|
G | A | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.765-1295G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 5/12 | chr3 | 142779539 | ||||||
| chr3:142779633
|
T | G | 2 | a0001c0002t0001g0044a0001c0002t0001g0050 | 2 | NA18967.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.765-1201T>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 5/12 | chr3 | 142779633 | ||||||
| chr3:142779839
|
A | T | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.765-995A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 5/12 | chr3 | 142779839 | ||||||
| chr3:142779854
|
G | A | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283 | 3 | HG01496.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.765-980G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 5/12 | chr3 | 142779854 | ||||||
| chr3:142779861
|
A | AT | 19 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0183others(16): Show | 19 | HG00735.hp1 HG01070.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.765-952dupT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr3 | 142779861 | |||||
| chr3:142779861
|
AT | A | 83 | a0001c0001t0001g0080a0001c0001t0002g0309a0001c0001t0007g0107others(80): Show | 93 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.765-952delT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr3 | 142779861 | |||||
| chr3:142779861
|
ATT | A | 26 | a0001c0002t0001g0031a0001c0002t0001g0032a0001c0002t0001g0048others(23): Show | 31 | HG00621.hp1 HG01884.hp1 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.765-953_765-952del others(2): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr3 | 142779861 | |||||
| chr3:142780023
|
T | G | 12 | a0001c0003t0001g0033a0002c0005t0007g0026a0002c0005t0007g0027others(9): Show | 12 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.765-811T>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 5/12 | chr3 | 142780023 | ||||||
| chr3:142780366
|
A | T | 1 | a0001c0003t0006g0238 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.765-468A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 5/12 | chr3 | 142780366 | ||||||
| chr3:142780422
|
T | C | 20 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(17): Show | 24 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.765-412T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 5/12 | chr3 | 142780422 | ||||||
| chr3:142780483
|
G | A | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.765-351G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 5/12 | chr3 | 142780483 | ||||||
| chr3:142780641
|
G | A | 1 | a0001c0003t0006g0241 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.765-193G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 5/12 | chr3 | 142780641 | ||||||
| chr3:142780661
|
T | A | 3 | a0001c0003t0001g0254a0001c0003t0001g0262a0001c0003t0001g0263 | 3 | HG00735.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.765-173T>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 5/12 | chr3 | 142780661 | ||||||
| chr3:142781230
|
C | T | 4 | a0001c0003t0003g0006a0001c0003t0003g0073a0001c0003t0003g0074others(1): Show | 5 | HG01884.hp1 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.960+201C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | chr3 | 142781230 | ||||||
| chr3:142781305
|
T | C | 14 | a0001c0001t0001g0007a0001c0001t0001g0071a0001c0001t0001g0072others(11): Show | 15 | HG00438.hp2 HG00673.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.960+276T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | chr3 | 142781305 | ||||||
| chr3:142781348
|
A | G | 3 | a0001c0003t0006g0245a0001c0003t0006g0246a0001c0003t0006g0249 | 3 | HG03017.hp1 HG03688.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.960+319A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | chr3 | 142781348 | ||||||
| chr3:142781394
|
C | T | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.960+365C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | chr3 | 142781394 | ||||||
| chr3:142781439
|
T | C | 2 | a0001c0002t0001g0012a0001c0002t0001g0219 | 3 | HG02056.hp2 HG02071.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.960+410T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | chr3 | 142781439 | ||||||
| chr3:142781490
|
A | G | 1 | a0002c0005t0007g0070 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.960+461A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | chr3 | 142781490 | ||||||
| chr3:142781638
|
T | C | 17 | a0001c0001t0003g0020a0001c0001t0003g0284a0001c0001t0003g0285others(14): Show | 18 | HG00323.hp1 HG00738.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.960+609T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | chr3 | 142781638 | ||||||
| chr3:142781682
|
T | C | 9 | a0001c0001t0001g0146a0001c0001t0001g0157a0001c0001t0008g0138others(6): Show | 9 | HG01243.hp1 HG02145.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.960+653T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | chr3 | 142781682 | ||||||
| chr3:142782085
|
G | C | 4 | a0001c0003t0003g0006a0001c0003t0003g0073a0001c0003t0003g0074others(1): Show | 5 | HG01884.hp1 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.960+1056G>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | chr3 | 142782085 | ||||||
| chr3:142782121
|
A | T | 1 | a0001c0004t0014g0269 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.960+1092A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | chr3 | 142782121 | ||||||
| chr3:142782289
|
A | T | 9 | a0001c0003t0006g0014a0001c0003t0006g0015a0001c0003t0006g0237others(6): Show | 11 | HG02257.hp1 HG02280.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.960+1260A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | chr3 | 142782289 | ||||||
| chr3:142782351
|
A | G | 1 | a0001c0001t0007g0107 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.960+1322A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | chr3 | 142782351 | ||||||
| chr3:142782429
|
G | GT | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.960+1403dupT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr3 | 142782429 | |||||
| chr3:142782461
|
T | C | 164 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(161): Show | 185 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.960+1432T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | chr3 | 142782461 | ||||||
| chr3:142782538
|
C | T | 4 | a0001c0003t0003g0006a0001c0003t0003g0073a0001c0003t0003g0074others(1): Show | 5 | HG01884.hp1 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.960+1509C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | chr3 | 142782538 | ||||||
| chr3:142782574
|
G | A | 1 | a0001c0001t0003g0286 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.960+1545G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | chr3 | 142782574 | ||||||
| chr3:142782583
|
C | G | 1 | a0001c0003t0001g0242 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.960+1554C>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | chr3 | 142782583 | ||||||
| chr3:142782631
|
T | C | 1 | a0001c0001t0003g0286 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.960+1602T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | chr3 | 142782631 | ||||||
| chr3:142782698
|
G | A | 1 | a0001c0001t0003g0289 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.960+1669G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | chr3 | 142782698 | ||||||
| chr3:142782699
|
G | A | 1 | a0001c0006t0001g0305 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.960+1670G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | chr3 | 142782699 | ||||||
| chr3:142782712
|
T | TG | 18 | a0001c0003t0004g0002a0001c0003t0004g0004a0001c0003t0004g0005others(15): Show | 22 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.960+1684dupG | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr3 | 142782712 | |||||
| chr3:142782740
|
A | G | 18 | a0001c0003t0004g0002a0001c0003t0004g0004a0001c0003t0004g0005others(15): Show | 22 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.960+1711A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | chr3 | 142782740 | ||||||
| chr3:142783165
|
A | C | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.961-1539A>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | chr3 | 142783165 | ||||||
| chr3:142783319
|
C | T | 2 | a0001c0008t0009g0024a0001c0008t0009g0025 | 2 | HG01255.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.961-1385C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | chr3 | 142783319 | ||||||
| chr3:142783362
|
A | G | 18 | a0001c0003t0004g0002a0001c0003t0004g0004a0001c0003t0004g0005others(15): Show | 22 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.961-1342A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | chr3 | 142783362 | ||||||
| chr3:142783463
|
A | G | 1 | a0002c0005t0007g0070 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.961-1241A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | chr3 | 142783463 | ||||||
| chr3:142783891
|
A | T | 1 | a0001c0001t0002g0148 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.961-813A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | chr3 | 142783891 | ||||||
| chr3:142784023
|
C | T | 18 | a0001c0004t0005g0017a0001c0004t0005g0018a0001c0004t0005g0019others(15): Show | 21 | HG00673.hp2 HG00738.hp2 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.961-681C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | chr3 | 142784023 | ||||||
| chr3:142784157
|
G | T | 164 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(161): Show | 185 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.961-547G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | chr3 | 142784157 | ||||||
| chr3:142784320
|
T | TTAATACT others(95): Show |
6 | a0001c0003t0001g0016a0001c0003t0001g0252a0001c0003t0001g0280others(3): Show | 7 | HG01891.hp1 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.961-372_961-371ins others(102): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr3 | 142784320 | |||||
| chr3:142784320
|
T | TTAATACT others(97): Show |
25 | a0001c0003t0001g0240a0001c0003t0001g0242a0001c0003t0001g0254others(22): Show | 27 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.961-372_961-371ins others(104): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr3 | 142784320 | |||||
| chr3:142784320
|
T | TTAATACT others(99): Show |
2 | a0001c0008t0009g0024a0001c0008t0009g0025 | 2 | HG01255.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.961-372_961-371ins others(106): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr3 | 142784320 | |||||
| chr3:142784353
|
C | T | 40 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(37): Show | 43 | HG00597.hp1 HG00642.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.961-351C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | chr3 | 142784353 | ||||||
| chr3:142784436
|
T | C | 134 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(131): Show | 150 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.961-268T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 6/12 | chr3 | 142784436 | ||||||
| chr3:142785069
|
T | A | 2 | a0001c0001t0001g0185a0001c0001t0001g0196 | 2 | HG01261.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1297+29T>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142785069 | ||||||
| chr3:142785242
|
ATC | A | 55 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0031others(52): Show | 65 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.1297+208_1297+209d others(4): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr3 | 142785242 | |||||
| chr3:142785594
|
C | T | 1 | a0001c0003t0001g0261 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1297+554C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142785594 | ||||||
| chr3:142785608
|
T | C | 33 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(30): Show | 36 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.1297+568T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142785608 | ||||||
| chr3:142785775
|
A | G | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1297+735A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142785775 | ||||||
| chr3:142786088
|
A | G | 1 | a0001c0002t0001g0042 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1297+1048A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142786088 | ||||||
| chr3:142786247
|
T | G | 1 | a0001c0001t0002g0148 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1297+1207T>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142786247 | ||||||
| chr3:142786290
|
A | G | 4 | a0001c0003t0003g0006a0001c0003t0003g0073a0001c0003t0003g0074others(1): Show | 5 | HG01884.hp1 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1297+1250A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142786290 | ||||||
| chr3:142786305
|
C | A | 1 | a0002c0005t0007g0037 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1297+1265C>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142786305 | ||||||
| chr3:142786374
|
T | A | 2 | a0001c0002t0001g0217a0001c0002t0001g0223 | 2 | HG00323.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.1297+1334T>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142786374 | ||||||
| chr3:142786628
|
C | T | 164 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(161): Show | 185 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1297+1588C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142786628 | ||||||
| chr3:142787060
|
G | A | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG00438.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.1297+2020G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142787060 | ||||||
| chr3:142787080
|
C | T | 1 | a0001c0002t0001g0311 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1297+2040C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142787080 | ||||||
| chr3:142787332
|
T | C | 1 | a0001c0003t0010g0022 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1297+2292T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142787332 | ||||||
| chr3:142787457
|
G | GA | 20 | a0001c0002t0001g0279a0001c0004t0005g0017a0001c0004t0005g0018others(17): Show | 23 | HG00673.hp2 HG00738.hp2 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.1297+2423dupA | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr3 | 142787457 | |||||
| chr3:142787661
|
G | A | 1 | a0001c0001t0003g0285 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1297+2621G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142787661 | ||||||
| chr3:142787808
|
T | C | 3 | a0001c0003t0004g0002a0001c0003t0004g0058a0001c0003t0004g0068 | 6 | NA18963.hp1 NA18971.hp2 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.1297+2768T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142787808 | ||||||
| chr3:142787986
|
A | C | 2 | a0001c0008t0009g0024a0001c0008t0009g0025 | 2 | HG01255.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1297+2946A>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142787986 | ||||||
| chr3:142788070
|
A | G | 14 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(11): Show | 15 | HG00735.hp2 HG01109.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1298-2949A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142788070 | ||||||
| chr3:142788107
|
T | G | 1 | a0001c0003t0010g0022 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1298-2912T>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142788107 | ||||||
| chr3:142788120
|
G | A | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283 | 3 | HG01496.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1298-2899G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142788120 | ||||||
| chr3:142788323
|
AAGAG | A | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1298-2692_1298-268 others(8): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr3 | 142788323 | |||||
| chr3:142788676
|
G | T | 1 | a0001c0003t0004g0064 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1298-2343G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142788676 | ||||||
| chr3:142788735
|
T | C | 4 | a0001c0002t0001g0207a0001c0002t0001g0211a0001c0002t0001g0212others(1): Show | 4 | HG01934.hp1 HG01978.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.1298-2284T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142788735 | ||||||
| chr3:142788767
|
C | T | 2 | a0001c0002t0001g0031a0001c0002t0001g0032 | 2 | HG02630.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1298-2252C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142788767 | ||||||
| chr3:142789026
|
A | G | 4 | a0001c0003t0003g0006a0001c0003t0003g0073a0001c0003t0003g0074others(1): Show | 5 | HG01884.hp1 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1298-1993A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142789026 | ||||||
| chr3:142789124
|
G | A | 8 | a0001c0001t0003g0291a0001c0001t0003g0292a0001c0001t0003g0293others(5): Show | 8 | HG00738.hp1 HG01074.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1298-1895G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142789124 | ||||||
| chr3:142789152
|
C | T | 1 | a0001c0001t0008g0138 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1298-1867C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142789152 | ||||||
| chr3:142789319
|
C | CTCCTTCC others(10): Show |
2 | a0001c0001t0001g0185a0001c0001t0001g0196 | 2 | HG01261.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1298-1700_1298-169 others(21): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142789319 | ||||||
| chr3:142789377
|
A | T | 10 | a0001c0004t0005g0017a0001c0004t0005g0019a0001c0004t0005g0267others(7): Show | 12 | NA18985.hp1 NA18994.hp2 NA18999.hp2 others(9): Show |
intron_variant | MODIFIER | c.1298-1642A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142789377 | ||||||
| chr3:142789682
|
G | T | 2 | a0001c0004t0005g0267a0001c0004t0005g0277 | 2 | NA18985.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1298-1337G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142789682 | ||||||
| chr3:142789755
|
G | A | 1 | a0002c0005t0007g0036 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1298-1264G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142789755 | ||||||
| chr3:142789778
|
T | G | 1 | a0001c0001t0001g0179 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1298-1241T>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142789778 | ||||||
| chr3:142789910
|
C | T | 33 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(30): Show | 36 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.1298-1109C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142789910 | ||||||
| chr3:142790092
|
A | G | 4 | a0001c0003t0003g0006a0001c0003t0003g0073a0001c0003t0003g0074others(1): Show | 5 | HG01884.hp1 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1298-927A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142790092 | ||||||
| chr3:142790249
|
C | G | 1 | a0001c0003t0004g0069 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1298-770C>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142790249 | ||||||
| chr3:142790397
|
G | C | 134 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(131): Show | 150 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.1298-622G>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142790397 | ||||||
| chr3:142790509
|
A | C | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1298-510A>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142790509 | ||||||
| chr3:142790644
|
G | A | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1298-375G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142790644 | ||||||
| chr3:142790682
|
C | T | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1298-337C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142790682 | ||||||
| chr3:142790789
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1298-230T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142790789 | ||||||
| chr3:142790830
|
C | T | 20 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(17): Show | 24 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.1298-189C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | chr3 | 142790830 | ||||||
| chr3:142790896
|
G | GT | 163 | a0001c0001t0002g0309a0001c0002t0001g0001a0001c0002t0001g0003others(160): Show | 183 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.1298-114dupT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr3 | 142790896 | |||||
| chr3:142790955
|
GTAT | G | 18 | a0001c0003t0004g0002a0001c0003t0004g0004a0001c0003t0004g0005others(15): Show | 22 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.1298-59_1298-57del others(3): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr3 | 142790955 | |||||
| chr3:142791481
|
C | T | 1 | a0001c0003t0001g0263 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1437+323C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 8/12 | chr3 | 142791481 | ||||||
| chr3:142791506
|
G | A | 144 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(141): Show | 161 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.1437+348G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 8/12 | chr3 | 142791506 | ||||||
| chr3:142791624
|
A | G | 12 | a0001c0003t0001g0033a0002c0005t0007g0026a0002c0005t0007g0027others(9): Show | 12 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1437+466A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 8/12 | chr3 | 142791624 | ||||||
| chr3:142791986
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1437+828A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 8/12 | chr3 | 142791986 | ||||||
| chr3:142792089
|
A | G | 3 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0198 | 3 | NA18989.hp2 NA19054.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1438-735A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 8/12 | chr3 | 142792089 | ||||||
| chr3:142792369
|
G | A | 30 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(27): Show | 33 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1438-455G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 8/12 | chr3 | 142792369 | ||||||
| chr3:142792491
|
A | G | 4 | a0001c0006t0001g0303a0001c0006t0001g0304a0001c0006t0001g0305others(1): Show | 4 | HG02280.hp2 HG02451.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1438-333A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 8/12 | chr3 | 142792491 | ||||||
| chr3:142792620
|
A | C | 23 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0031others(20): Show | 30 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.1438-204A>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 8/12 | chr3 | 142792620 | ||||||
| chr3:142793319
|
T | G | 1 | a0002c0009t0007g0038 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1581+352T>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142793319 | ||||||
| chr3:142793410
|
G | A | 18 | a0001c0003t0004g0002a0001c0003t0004g0004a0001c0003t0004g0005others(15): Show | 22 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.1581+443G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142793410 | ||||||
| chr3:142794072
|
A | T | 2 | a0001c0001t0002g0137a0001c0001t0002g0149 | 2 | NA18973.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.1581+1105A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142794072 | ||||||
| chr3:142794095
|
C | A | 33 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(30): Show | 36 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.1581+1128C>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142794095 | ||||||
| chr3:142794125
|
T | C | 33 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(30): Show | 36 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.1581+1158T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142794125 | ||||||
| chr3:142794143
|
A | G | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283 | 3 | HG01496.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1581+1176A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142794143 | ||||||
| chr3:142794153
|
A | G | 1 | a0001c0001t0002g0123 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1581+1186A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142794153 | ||||||
| chr3:142794248
|
T | C | 1 | a0001c0004t0005g0275 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1581+1281T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142794248 | ||||||
| chr3:142794256
|
GA | G | 18 | a0001c0003t0004g0002a0001c0003t0004g0004a0001c0003t0004g0005others(15): Show | 22 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.1581+1290delA | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142794256 | ||||||
| chr3:142794515
|
C | G | 1 | a0001c0002t0001g0227 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1581+1548C>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142794515 | ||||||
| chr3:142794662
|
G | A | 1 | a0001c0002t0001g0224 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1581+1695G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142794662 | ||||||
| chr3:142794726
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1581+1759C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142794726 | ||||||
| chr3:142794835
|
T | C | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG03669.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1581+1868T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142794835 | ||||||
| chr3:142795053
|
G | T | 134 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(131): Show | 150 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.1581+2086G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142795053 | ||||||
| chr3:142795133
|
C | T | 2 | a0001c0008t0009g0024a0001c0008t0009g0025 | 2 | HG01255.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1581+2166C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142795133 | ||||||
| chr3:142795136
|
G | A | 20 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(17): Show | 24 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.1581+2169G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142795136 | ||||||
| chr3:142795231
|
T | C | 164 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(161): Show | 185 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1581+2264T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142795231 | ||||||
| chr3:142795345
|
C | CAG | 168 | a0001c0001t0001g0077a0001c0001t0001g0281a0001c0001t0001g0282others(165): Show | 189 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.1581+2379_1581+238 others(6): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr3 | 142795345 | |||||
| chr3:142795417
|
G | T | 97 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(94): Show | 109 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.1581+2450G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142795417 | ||||||
| chr3:142795468
|
G | C | 10 | a0001c0006t0001g0021a0001c0006t0001g0300a0001c0006t0001g0301others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1581+2501G>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142795468 | ||||||
| chr3:142795579
|
G | GAA | 17 | a0001c0003t0004g0002a0001c0003t0004g0004a0001c0003t0004g0005others(14): Show | 21 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.1581+2621_1581+262 others(6): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr3 | 142795579 | |||||
| chr3:142795712
|
G | A | 1 | a0001c0003t0001g0258 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1581+2745G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142795712 | ||||||
| chr3:142795831
|
C | T | 164 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(161): Show | 185 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1581+2864C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142795831 | ||||||
| chr3:142796185
|
G | C | 1 | a0001c0002t0001g0227 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1581+3218G>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142796185 | ||||||
| chr3:142796197
|
T | C | 12 | a0001c0003t0001g0033a0002c0005t0007g0026a0002c0005t0007g0027others(9): Show | 12 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1581+3230T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142796197 | ||||||
| chr3:142796599
|
ACT | A | 4 | a0001c0003t0003g0006a0001c0003t0003g0073a0001c0003t0003g0074others(1): Show | 5 | HG01884.hp1 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1581+3635_1581+363 others(6): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr3 | 142796599 | |||||
| chr3:142796608
|
CGTGG | C | 3 | a0001c0003t0001g0016a0001c0003t0001g0252a0001c0003t0011g0251 | 4 | HG01891.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1581+3644_1581+364 others(8): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr3 | 142796608 | |||||
| chr3:142796616
|
C | T | 3 | a0001c0003t0001g0016a0001c0003t0001g0252a0001c0003t0011g0251 | 4 | HG01891.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1581+3649C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142796616 | ||||||
| chr3:142796617
|
C | T | 3 | a0001c0003t0001g0016a0001c0003t0001g0252a0001c0003t0011g0251 | 4 | HG01891.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1581+3650C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142796617 | ||||||
| chr3:142796618
|
T | G | 3 | a0001c0003t0001g0016a0001c0003t0001g0252a0001c0003t0011g0251 | 4 | HG01891.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1581+3651T>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142796618 | ||||||
| chr3:142796679
|
A | AC | 164 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(161): Show | 185 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1581+3712_1581+371 others(5): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142796679 | ||||||
| chr3:142796929
|
T | C | 5 | a0002c0005t0007g0034a0002c0005t0007g0035a0002c0005t0007g0036others(2): Show | 5 | HG01123.hp1 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1581+3962T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142796929 | ||||||
| chr3:142797015
|
T | A | 1 | a0001c0001t0001g0187 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1581+4048T>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142797015 | ||||||
| chr3:142797034
|
G | A | 1 | a0001c0003t0010g0022 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1581+4067G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142797034 | ||||||
| chr3:142797052
|
AC | A | 20 | a0001c0003t0001g0023a0001c0003t0004g0002a0001c0003t0004g0004others(17): Show | 24 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.1581+4087delC | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr3 | 142797052 | |||||
| chr3:142797073
|
T | TAAGA | 55 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0031others(52): Show | 65 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.1581+4108_1581+411 others(8): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr3 | 142797073 | |||||
| chr3:142797175
|
G | GT | 15 | a0001c0001t0001g0077a0001c0001t0001g0158a0001c0001t0001g0185others(12): Show | 16 | HG01109.hp1 HG01433.hp2 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.1581+4222dupT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr3 | 142797175 | |||||
| chr3:142797175
|
GT | G | 23 | a0001c0002t0001g0031a0001c0002t0001g0032a0001c0002t0001g0279others(20): Show | 26 | HG00673.hp2 HG00738.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.1581+4222delT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr3 | 142797175 | |||||
| chr3:142797175
|
GTT | G | 21 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0039others(18): Show | 28 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(25): Show |
intron_variant | MODIFIER | c.1581+4221_1581+422 others(6): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr3 | 142797175 | |||||
| chr3:142797382
|
C | G | 1 | a0001c0004t0005g0274 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1581+4415C>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142797382 | ||||||
| chr3:142797525
|
A | T | 167 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(164): Show | 188 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.1581+4558A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142797525 | ||||||
| chr3:142797812
|
C | A | 1 | a0001c0001t0001g0176 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1582-4357C>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142797812 | ||||||
| chr3:142797984
|
G | A | 23 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0031others(20): Show | 30 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.1582-4185G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142797984 | ||||||
| chr3:142797990
|
T | C | 2 | a0001c0008t0009g0024a0001c0008t0009g0025 | 2 | HG01255.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1582-4179T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142797990 | ||||||
| chr3:142798257
|
A | G | 3 | a0001c0001t0001g0120a0001c0001t0001g0189a0001c0001t0001g0195 | 3 | NA18970.hp2 NA19007.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1582-3912A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142798257 | ||||||
| chr3:142798321
|
G | A | 164 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(161): Show | 185 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1582-3848G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142798321 | ||||||
| chr3:142798565
|
C | T | 6 | a0001c0001t0001g0146a0001c0001t0008g0138a0001c0001t0008g0139others(3): Show | 6 | HG01243.hp1 HG02145.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1582-3604C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142798565 | ||||||
| chr3:142798763
|
C | A | 2 | a0003c0007t0001g0204a0003c0007t0001g0235 | 2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1582-3406C>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142798763 | ||||||
| chr3:142798866
|
T | C | 2 | a0001c0003t0001g0023a0001c0003t0010g0022 | 2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1582-3303T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142798866 | ||||||
| chr3:142799113
|
C | A | 9 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(6): Show | 10 | HG00735.hp2 HG01891.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.1582-3056C>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142799113 | ||||||
| chr3:142799195
|
CTCTG | C | 18 | a0001c0003t0004g0002a0001c0003t0004g0004a0001c0003t0004g0005others(15): Show | 22 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.1582-2972_1582-296 others(8): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr3 | 142799195 | |||||
| chr3:142799470
|
C | T | 97 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(94): Show | 109 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.1582-2699C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142799470 | ||||||
| chr3:142799509
|
C | CT | 3 | a0001c0003t0006g0245a0001c0003t0006g0246a0001c0003t0006g0249 | 3 | HG03017.hp1 HG03688.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1582-2659dupT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr3 | 142799509 | |||||
| chr3:142799527
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1582-2642C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142799527 | ||||||
| chr3:142799529
|
G | A | 1 | a0001c0002t0001g0312 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1582-2640G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142799529 | ||||||
| chr3:142799539
|
A | T | 31 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(28): Show | 34 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1582-2630A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142799539 | ||||||
| chr3:142799692
|
A | G | 42 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0104others(39): Show | 44 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.1582-2477A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142799692 | ||||||
| chr3:142799869
|
C | T | 18 | a0001c0003t0004g0002a0001c0003t0004g0004a0001c0003t0004g0005others(15): Show | 22 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.1582-2300C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142799869 | ||||||
| chr3:142799937
|
A | G | 1 | a0001c0003t0003g0075 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1582-2232A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142799937 | ||||||
| chr3:142800093
|
A | G | 1 | a0001c0001t0003g0289 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1582-2076A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142800093 | ||||||
| chr3:142800378
|
G | A | 3 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0002g0152 | 3 | NA18957.hp1 NA19082.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1582-1791G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142800378 | ||||||
| chr3:142800380
|
T | G | 1 | a0001c0001t0001g0189 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1582-1789T>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142800380 | ||||||
| chr3:142800498
|
G | A | 3 | a0001c0001t0001g0183a0001c0001t0003g0110a0001c0001t0003g0135 | 3 | HG00735.hp1 HG01106.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.1582-1671G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142800498 | ||||||
| chr3:142800606
|
C | T | 42 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0104others(39): Show | 44 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.1582-1563C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142800606 | ||||||
| chr3:142800918
|
G | A | 164 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(161): Show | 185 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1582-1251G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142800918 | ||||||
| chr3:142800922
|
GA | G | 27 | a0001c0001t0008g0138a0001c0003t0001g0033a0001c0003t0003g0006others(24): Show | 32 | HG00673.hp2 HG00738.hp2 HG01346.hp2 others(29): Show |
intron_variant | MODIFIER | c.1582-1233delA | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr3 | 142800922 | |||||
| chr3:142801049
|
AATAT | A | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283 | 3 | HG01496.hp1 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1582-1119_1582-111 others(8): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142801049 | ||||||
| chr3:142801101
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1582-1068T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142801101 | ||||||
| chr3:142801123
|
G | A | 19 | a0001c0004t0005g0017a0001c0004t0005g0018a0001c0004t0005g0019others(16): Show | 22 | HG00673.hp2 HG00738.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.1582-1046G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142801123 | ||||||
| chr3:142801248
|
G | A | 44 | a0001c0001t0001g0176a0001c0003t0001g0016a0001c0003t0001g0240others(41): Show | 48 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.1582-921G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142801248 | ||||||
| chr3:142801280
|
TTAAAAAA | T | 9 | a0001c0003t0006g0014a0001c0003t0006g0015a0001c0003t0006g0237others(6): Show | 11 | HG02257.hp1 HG02280.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1582-875_1582-869d others(9): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr3 | 142801280 | |||||
| chr3:142801343
|
ATGT | A | 101 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(98): Show | 114 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.1582-823_1582-821d others(5): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr3 | 142801343 | |||||
| chr3:142801551
|
A | G | 1 | a0001c0001t0001g0283 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1582-618A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142801551 | ||||||
| chr3:142801646
|
G | A | 2 | a0001c0003t0001g0023a0001c0003t0010g0022 | 2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1582-523G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142801646 | ||||||
| chr3:142801673
|
A | T | 1 | a0001c0002t0001g0202 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1582-496A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142801673 | ||||||
| chr3:142801857
|
T | G | 4 | a0001c0003t0003g0006a0001c0003t0003g0073a0001c0003t0003g0074others(1): Show | 5 | HG01884.hp1 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1582-312T>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142801857 | ||||||
| chr3:142801906
|
T | C | 1 | a0001c0003t0004g0062 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1582-263T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142801906 | ||||||
| chr3:142801919
|
C | T | 101 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(98): Show | 114 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.1582-250C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142801919 | ||||||
| chr3:142802058
|
G | A | 24 | a0001c0001t0001g0007a0001c0001t0001g0071a0001c0001t0001g0072others(21): Show | 25 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.1582-111G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 9/12 | chr3 | 142802058 | ||||||
| chr3:142802382
|
C | CT | 75 | a0001c0001t0001g0077a0001c0001t0001g0146a0001c0001t0001g0157others(72): Show | 79 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.1757+50dupT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr3 | 142802382 | |||||
| chr3:142802382
|
CT | C | 22 | a0001c0001t0001g0180a0001c0001t0001g0194a0001c0003t0001g0023others(19): Show | 26 | HG00621.hp1 HG00621.hp2 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.1757+50delT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr3 | 142802382 | |||||
| chr3:142802743
|
T | C | 3 | a0001c0003t0001g0258a0001c0003t0001g0259a0001c0003t0001g0260 | 3 | HG02486.hp2 HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1757+399T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 10/12 | chr3 | 142802743 | ||||||
| chr3:142802780
|
C | T | 115 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(112): Show | 128 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1757+436C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 10/12 | chr3 | 142802780 | ||||||
| chr3:142803278
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1758-699A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 10/12 | chr3 | 142803278 | ||||||
| chr3:142803309
|
A | G | 1 | a0001c0003t0010g0022 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1758-668A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 10/12 | chr3 | 142803309 | ||||||
| chr3:142803476
|
T | G | 1 | a0001c0001t0003g0298 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1758-501T>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 10/12 | chr3 | 142803476 | ||||||
| chr3:142803548
|
G | A | 145 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(142): Show | 163 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.1758-429G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 10/12 | chr3 | 142803548 | ||||||
| chr3:142803627
|
G | T | 42 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0104others(39): Show | 44 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.1758-350G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 10/12 | chr3 | 142803627 | ||||||
| chr3:142803755
|
G | T | 1 | a0001c0001t0001g0179 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1758-222G>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 10/12 | chr3 | 142803755 | ||||||
| chr3:142803804
|
G | A | 1 | a0002c0005t0007g0070 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1758-173G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 10/12 | chr3 | 142803804 | ||||||
| chr3:142803911
|
A | T | 42 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0104others(39): Show | 44 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.1758-66A>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 10/12 | chr3 | 142803911 | ||||||
| chr3:142804333
|
T | C | 3 | a0001c0003t0001g0016a0001c0003t0001g0252a0001c0003t0011g0251 | 4 | HG01891.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1960-103T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 11/12 | chr3 | 142804333 | ||||||
| chr3:142804640
|
T | C | 1 | a0001c0004t0005g0276 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2154+10T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | chr3 | 142804640 | ||||||
| chr3:142804713
|
G | A | 125 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(122): Show | 139 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.2154+83G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | chr3 | 142804713 | ||||||
| chr3:142804735
|
TCTGA | T | 23 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0031others(20): Show | 30 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.2154+108_2154+111d others(6): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr3 | 142804735 | |||||
| chr3:142805088
|
G | A | 1 | a0001c0004t0005g0275 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2154+458G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | chr3 | 142805088 | ||||||
| chr3:142805115
|
AACAAAT | A | 39 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0104others(36): Show | 41 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.2154+487_2154+492d others(8): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr3 | 142805115 | |||||
| chr3:142805119
|
A | AAT | 5 | a0001c0001t0001g0077a0001c0001t0002g0111a0001c0001t0002g0112others(2): Show | 5 | HG01433.hp2 HG02451.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.2154+499_2154+500d others(4): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr3 | 142805119 | |||||
| chr3:142805119
|
AATAT | A | 4 | a0001c0003t0003g0006a0001c0003t0003g0073a0001c0003t0003g0075others(1): Show | 5 | HG01884.hp1 HG02622.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2154+497_2154+500d others(6): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr3 | 142805119 | |||||
| chr3:142805125
|
TATATACA others(3): Show |
T | 16 | a0001c0002t0001g0032a0001c0002t0001g0046a0001c0002t0001g0047others(13): Show | 16 | HG01070.hp1 HG01123.hp1 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.2154+497_2154+506d others(12): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr3 | 142805125 | |||||
| chr3:142805125
|
TATATACA others(5): Show |
T | 17 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0039others(14): Show | 24 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(21): Show |
intron_variant | MODIFIER | c.2154+497_2154+508d others(14): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr3 | 142805125 | |||||
| chr3:142805127
|
T | C | 1 | a0001c0003t0003g0074 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2154+497T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | chr3 | 142805127 | ||||||
| chr3:142805127
|
TATACAC | T | 3 | a0001c0002t0001g0279a0001c0003t0010g0022a0001c0006t0001g0308 | 3 | HG02258.hp2 HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2154+499_2154+504d others(8): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr3 | 142805127 | |||||
| chr3:142805127
|
TATACACA others(1): Show |
T | 12 | a0001c0003t0001g0023a0001c0003t0001g0257a0001c0003t0001g0260others(9): Show | 13 | HG01109.hp1 HG02280.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2154+499_2154+506d others(10): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr3 | 142805127 | |||||
| chr3:142805127
|
TATACACA others(3): Show |
T | 4 | a0001c0003t0001g0254a0001c0003t0001g0262a0001c0003t0001g0263others(1): Show | 4 | HG00735.hp2 HG01255.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2154+499_2154+508d others(12): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr3 | 142805127 | |||||
| chr3:142805127
|
TATACACA others(5): Show |
T | 25 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(22): Show | 28 | HG00642.hp1 HG01175.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.2154+499_2154+510d others(14): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr3 | 142805127 | |||||
| chr3:142805127
|
TATACACA others(7): Show |
T | 1 | a0001c0008t0009g0024 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2154+499_2154+512d others(16): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr3 | 142805127 | |||||
| chr3:142805129
|
T | C | 6 | a0001c0001t0001g0007a0001c0001t0001g0101a0001c0001t0001g0161others(3): Show | 7 | HG02027.hp2 HG02615.hp1 NA18999.hp1 others(4): Show |
intron_variant | MODIFIER | c.2154+499T>C | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | chr3 | 142805129 | ||||||
| chr3:142805129
|
T | TAC | 13 | a0001c0001t0001g0088a0001c0001t0001g0153a0001c0001t0001g0154others(10): Show | 14 | HG00673.hp1 HG00673.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.2154+539_2154+540d others(4): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr3 | 142805129 | |||||
| chr3:142805129
|
T | TACAC | 5 | a0001c0001t0001g0011a0001c0001t0001g0192a0001c0001t0002g0137others(2): Show | 6 | HG01192.hp2 HG02055.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.2154+537_2154+540d others(6): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr3 | 142805129 | |||||
| chr3:142805129
|
TAC | T | 15 | a0001c0001t0001g0079a0001c0001t0001g0157a0001c0001t0001g0167others(12): Show | 15 | HG00408.hp2 HG00609.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.2154+539_2154+540d others(4): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr3 | 142805129 | |||||
| chr3:142805129
|
TACAC | T | 34 | a0001c0001t0001g0084a0001c0001t0001g0171a0001c0001t0001g0181others(31): Show | 36 | HG00323.hp1 HG00438.hp1 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.2154+537_2154+540d others(6): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr3 | 142805129 | |||||
| chr3:142805129
|
TACACAC | T | 31 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0199others(28): Show | 33 | HG00323.hp2 HG00423.hp1 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.2154+535_2154+540d others(8): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr3 | 142805129 | |||||
| chr3:142805129
|
TACACACA others(1): Show |
T | 3 | a0001c0002t0001g0214a0001c0002t0001g0215a0001c0002t0001g0217 | 3 | HG01081.hp2 NA18962.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2154+533_2154+540d others(10): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr3 | 142805129 | |||||
| chr3:142805129
|
TACACACA others(3): Show |
T | 18 | a0001c0003t0004g0002a0001c0003t0004g0004a0001c0003t0004g0005others(15): Show | 22 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.2154+531_2154+540d others(12): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr3 | 142805129 | |||||
| chr3:142805131
|
C | T | 16 | a0001c0001t0001g0146a0001c0001t0002g0111a0001c0001t0002g0112others(13): Show | 16 | HG01074.hp2 HG01243.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.2154+501C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | chr3 | 142805131 | ||||||
| chr3:142805133
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2154+503C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | chr3 | 142805133 | ||||||
| chr3:142805135
|
C | T | 6 | a0001c0001t0002g0009a0001c0001t0002g0094a0001c0001t0002g0109others(3): Show | 7 | NA18939.hp2 NA18948.hp2 NA18984.hp2 others(4): Show |
intron_variant | MODIFIER | c.2154+505C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | chr3 | 142805135 | ||||||
| chr3:142805203
|
A | AT | 145 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0012others(142): Show | 163 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.2154+584dupT | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr3 | 142805203 | |||||
| chr3:142805279
|
A | G | 35 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0031others(32): Show | 42 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.2154+649A>G | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | chr3 | 142805279 | ||||||
| chr3:142805442
|
T | A | 1 | a0001c0004t0005g0276 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2155-566T>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | chr3 | 142805442 | ||||||
| chr3:142805479
|
AAGC | A | 33 | a0001c0003t0001g0016a0001c0003t0001g0240a0001c0003t0001g0242others(30): Show | 36 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.2155-526_2155-524d others(5): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr3 | 142805479 | |||||
| chr3:142805520
|
CTT | C | 3 | a0001c0002t0001g0003a0001c0002t0001g0053a0001c0002t0001g0054 | 4 | HG00408.hp1 NA19054.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.2155-485_2155-484d others(4): Show |
TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr3 | 142805520 | |||||
| chr3:142805722
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2155-286G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | chr3 | 142805722 | ||||||
| chr3:142805774
|
G | A | 3 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0002g0152 | 3 | NA18957.hp1 NA19082.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2155-234G>A | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | chr3 | 142805774 | ||||||
| chr3:142805954
|
C | T | 22 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(19): Show | 25 | HG00673.hp2 HG00738.hp2 HG01346.hp2 others(22): Show |
intron_variant | MODIFIER | c.2155-54C>T | TRPC1 | ENSG00000144935.17 | transcript | ENST00000476941.6 | protein_coding | 12/12 | chr3 | 142805954 |