Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 729873 |
|---|---|
| ensemblid | ENSG00000274611.4 |
| hgncid | 19031 |
| symbol | TBC1D3 |
| name | TBC1 domain family member 3 |
| refseq_nuc | NM_001123391.4 |
| refseq_prot | NP_001116863.3 |
| ensembl_nuc | ENST00000620215.3 |
| ensembl_prot | ENSP00000478683.1 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 38181659 |
| end | 38192555 |
| strand | - |
| ver | v1.2 |
| region | chr17:38181659-38192555 |
| region5000 | chr17:38176659-38197555 |
| regionname0 | TBC1D3_chr17_38181659_38192555 |
| regionname5000 | TBC1D3_chr17_38176659_38197555 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 549 | 17 | 1 | 4 | 6 | 0 | 6 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0002 | 0/0 | 549 | 10 | 1 | 5 | 1 | 0 | 3 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0003 | 0/0 | 549 | 7 | 5 | 2 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0004 | 0/0 | 549 | 6 | 0 | 1 | 5 | 0 | 0 | 2 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0005 | 0/0 | 549 | 5 | 1 | 1 | 2 | 0 | 1 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0006 | 0/0 | 549 | 4 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0007 | 0/0 | 549 | 3 | 2 | 0 | 1 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0008 | 0/0 | 549 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0009 | 0/0 | 549 | 2 | 0 | 1 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0010 | 0/0 | 549 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0011 | 0/0 | 549 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0012 | 0/0 | 549 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0013 | 0/0 | 549 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0014 | 0/0 | 549 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0015 | 0/0 | 549 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0016 | 0/0 | 549 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0017 | 0/0 | 549 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0018 | 0/0 | 549 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0019 | 0/0 | 549 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0020 | 0/0 | 549 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0021 | 0/0 | 549 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0022 | 0/0 | 401 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0023 | 0/0 | 549 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0024 | 0/0 | 549 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0025 | 0/0 | 549 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1650 | 17 | 1 | 4 | 6 | 0 | 6 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| c0002 | 0/0 | 1650 | 9 | 0 | 5 | 1 | 0 | 3 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| c0003 | 0/0 | 1650 | 6 | 0 | 1 | 5 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| c0004 | 0/0 | 1650 | 5 | 1 | 1 | 2 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| c0005 | 0/0 | 1650 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| c0006 | 0/0 | 1650 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| c0007 | 0/0 | 1650 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| c0008 | 0/0 | 1650 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| c0009 | 0/0 | 1650 | 2 | 0 | 1 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| c0010 | 0/0 | 1650 | 2 | 1 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| c0011 | 0/0 | 1650 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| c0012 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| c0013 | 0/0 | 1650 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| c0014 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| c0015 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| c0016 | 0/0 | 1650 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| c0017 | 0/0 | 1650 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| c0018 | 0/0 | 1650 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| c0019 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| c0020 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| c0021 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| c0022 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| c0023 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| c0024 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| c0025 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| c0026 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| c0027 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| c0028 | 0/0 | 1650 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| c0029 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| c0030 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| c0031 | 0/0 | 1650 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 427 | 51 | 9 | 14 | 18 | 0 | 10 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| t0002 | 0/0 | 427 | 10 | 6 | 2 | 1 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| t0003 | 0/0 | 427 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| t0004 | 0/0 | 427 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| t0005 | 0/0 | 427 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| t0006 | 0/0 | 427 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| t0007 | 0/0 | 427 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| t0008 | 0/0 | 427 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| t0009 | 0/0 | 427 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| t0010 | 0/0 | 427 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| 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 | 5 | 0 | 0 | 4 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1650 | 17 | 1 | 4 | 6 | 0 | 6 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0002c0002 | 0/0 | 1650 | 9 | 0 | 5 | 1 | 0 | 3 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0002c0023 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0003c0005 | 0/0 | 1650 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0003c0006 | 0/0 | 1650 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0003c0007 | 0/0 | 1650 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0004c0003 | 0/0 | 1650 | 6 | 0 | 1 | 5 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0005c0004 | 0/0 | 1650 | 5 | 1 | 1 | 2 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0006c0008 | 0/0 | 1650 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0006c0016 | 0/0 | 1650 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0006c0018 | 0/0 | 1650 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0007c0010 | 0/0 | 1650 | 2 | 1 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0007c0025 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0008c0011 | 0/0 | 1650 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0009c0009 | 0/0 | 1650 | 2 | 0 | 1 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0010c0012 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0011c0022 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0012c0029 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0013c0027 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0014c0030 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0015c0024 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0016c0026 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0017c0014 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0018c0017 | 0/0 | 1650 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0019c0020 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0020c0015 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0021c0019 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0022c0021 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0023c0013 | 0/0 | 1650 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0024c0028 | 0/0 | 1650 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0025c0031 | 0/0 | 1650 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2076 | 17 | 1 | 4 | 6 | 0 | 6 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0002c0002t0001 | 0/0 | 2076 | 9 | 0 | 5 | 1 | 0 | 3 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0002c0023t0007 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0003c0005t0001 | 0/0 | 2076 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0003c0006t0004 | 0/0 | 2076 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0003c0007t0002 | 0/0 | 2076 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0004c0003t0001 | 0/0 | 2076 | 6 | 0 | 1 | 5 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0005c0004t0001 | 0/0 | 2076 | 4 | 1 | 1 | 2 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0005c0004t0002 | 0/0 | 2076 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0006c0008t0005 | 0/0 | 2076 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0006c0016t0002 | 0/0 | 2076 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0006c0018t0002 | 0/0 | 2076 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0007c0010t0002 | 0/0 | 2076 | 2 | 1 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0007c0025t0002 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0008c0011t0003 | 0/0 | 2076 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0009c0009t0001 | 0/0 | 2076 | 2 | 0 | 1 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0010c0012t0001 | 0/0 | 2076 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0011c0022t0001 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0012c0029t0009 | 0/0 | 2076 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0013c0027t0001 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0014c0030t0001 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0015c0024t0006 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0016c0026t0002 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0017c0014t0002 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0018c0017t0001 | 0/0 | 2076 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0019c0020t0001 | 0/0 | 2076 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0020c0015t0001 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0021c0019t0008 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0022c0021t0001 | 0/0 | 2076 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0023c0013t0010 | 0/0 | 2076 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0024c0028t0001 | 0/0 | 2076 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| a0025c0031t0001 | 0/0 | 2076 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | copy fasta | chr17 | 38176659 | 38197555 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0002c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0002c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0002c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0002c0023t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0003c0005t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0003c0005t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0003c0006t0004g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0003c0006t0004g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0003c0007t0002g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0004c0003t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0004c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0004c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0004c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0004c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0004c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0005c0004t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0005c0004t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0005c0004t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0005c0004t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0005c0004t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0006c0008t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0006c0008t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0006c0016t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0006c0018t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0007c0010t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0007c0010t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0007c0025t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0008c0011t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0008c0011t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0009c0009t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0009c0009t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0010c0012t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0011c0022t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0012c0029t0009g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0013c0027t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0014c0030t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0015c0024t0006g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0016c0026t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0017c0014t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0018c0017t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0019c0020t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0020c0015t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0021c0019t0008g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0022c0021t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0023c0013t0010g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0024c0028t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| a0025c0031t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG00438 | hp2 | a0005 | c0004 | t0001 | g0066 | EAS | CHS | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG00597 | hp1 | a0010 | c0012 | t0001 | g0048 | EAS | CHS | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG01070 | hp1 | a0018 | c0017 | t0001 | g0034 | AMR | PUR | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG01070 | hp2 | a0004 | c0003 | t0001 | g0018 | AMR | PUR | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG01071 | hp1 | a0025 | c0031 | t0001 | g0024 | AMR | PUR | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG01099 | hp1 | a0006 | c0018 | t0002 | g0010 | AMR | PUR | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG01099 | hp2 | a0005 | c0004 | t0001 | g0042 | AMR | PUR | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0027 | AMR | CLM | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG01261 | hp2 | a0009 | c0009 | t0001 | g0053 | AMR | CLM | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0031 | AMR | CLM | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG01361 | hp1 | a0003 | c0006 | t0004 | g0013 | AMR | CLM | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG01361 | hp2 | a0003 | c0006 | t0004 | g0012 | AMR | CLM | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG01433 | hp1 | a0006 | c0016 | t0002 | g0009 | AMR | CLM | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0032 | AMR | CLM | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG02027 | hp1 | a0005 | c0004 | t0001 | g0043 | EAS | KHV | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG02027 | hp2 | a0004 | c0003 | t0001 | g0037 | EAS | KHV | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG02040 | hp2 | a0004 | c0003 | t0001 | g0039 | EAS | KHV | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG02083 | hp2 | a0009 | c0009 | t0001 | g0056 | EAS | KHV | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG02129 | hp1 | a0004 | c0003 | t0001 | g0040 | EAS | KHV | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG02129 | hp2 | a0019 | c0020 | t0001 | g0054 | EAS | KHV | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0030 | AMR | PEL | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0026 | AMR | PEL | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG02451 | hp1 | a0014 | c0030 | t0001 | g0029 | AFR | ACB | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG02451 | hp2 | a0003 | c0005 | t0001 | g0003 | AFR | ACB | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG02717 | hp1 | a0003 | c0007 | t0002 | g0002 | AFR | GWD | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG02717 | hp2 | a0006 | c0008 | t0005 | g0016 | AFR | GWD | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG02723 | hp1 | a0003 | c0007 | t0002 | g0002 | AFR | GWD | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG02723 | hp2 | a0006 | c0008 | t0005 | g0014 | AFR | GWD | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0020 | SAS | PJL | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG02809 | hp1 | a0003 | c0005 | t0001 | g0003 | AFR | GWD | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG02809 | hp2 | a0008 | c0011 | t0003 | g0006 | AFR | GWD | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG02818 | hp1 | a0017 | c0014 | t0002 | g0046 | AFR | GWD | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG02818 | hp2 | a0007 | c0010 | t0002 | g0015 | AFR | GWD | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG03017 | hp2 | a0005 | c0004 | t0002 | g0044 | SAS | PJL | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG03041 | hp1 | a0016 | c0026 | t0002 | g0011 | AFR | GWD | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG03041 | hp2 | a0007 | c0025 | t0002 | g0047 | AFR | GWD | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG03453 | hp1 | a0011 | c0022 | t0001 | g0021 | AFR | MSL | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG03453 | hp2 | a0002 | c0023 | t0007 | g0036 | AFR | MSL | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0007 | SAS | PJL | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG03579 | hp1 | a0008 | c0011 | t0003 | g0005 | AFR | MSL | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG03579 | hp2 | a0015 | c0024 | t0006 | g0004 | AFR | MSL | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | STU | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | STU | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| HG04228 | hp2 | a0023 | c0013 | t0010 | g0023 | SAS | STU | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| NA18747 | hp1 | a0012 | c0029 | t0009 | g0019 | EAS | CHB | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHB | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| NA18950 | hp1 | a0007 | c0010 | t0002 | g0035 | EAS | JPT | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| NA18950 | hp2 | a0004 | c0003 | t0001 | g0041 | EAS | JPT | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| NA19043 | hp1 | a0013 | c0027 | t0001 | g0022 | AFR | LWK | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| NA19043 | hp2 | a0005 | c0004 | t0001 | g0045 | AFR | LWK | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| NA19084 | hp1 | a0004 | c0003 | t0001 | g0038 | EAS | JPT | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| NA19084 | hp2 | a0022 | c0021 | t0001 | g0055 | EAS | JPT | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0025 | SAS | GIH | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| NA20905 | hp2 | a0024 | c0028 | t0001 | g0063 | SAS | GIH | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| NA20300 | hp1 | a0020 | c0015 | t0001 | g0008 | AFR | USA | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | USA | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| NA21309 | hp1 | a0003 | c0005 | t0001 | g0033 | AFR | LWK | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| NA21309 | hp2 | a0021 | c0019 | t0008 | g0017 | AFR | LWK | TBC1D3_chr17_38176659_38197555 | TBC1D3 | chr17 | 38176659 | 38197555 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:38181659
|
T | G | 1 | a0012 | 1 | NA18747.hp1 | splice_region_variant | LOW | c.*315A>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 14/14 | chr17 | 38181659 | ||||||
| chr17:38182001
|
T | A | 4 | a0008a0015a0016others(1): Show | 5 | HG02809.hp2 HG03041.hp1 HG03579.hp1 others(2): Show |
missense_variant | MODERATE | c.1623A>T | p.Glu541Asp | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 14/14 | 1735/2077 | 1623/1650 | 541/549 | chr17 | 38182001 | ||
| chr17:38182047
|
T | G | 5 | a0001a0010a0019others(2): Show | 21 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(18): Show |
missense_variant | MODERATE | c.1577A>C | p.Gln526Pro | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 14/14 | 1689/2077 | 1577/1650 | 526/549 | chr17 | 38182047 | ||
| chr17:38182111
|
C | G | 1 | a0012 | 1 | NA18747.hp1 | missense_variant | MODERATE | c.1513G>C | p.Ala505Pro | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 14/14 | 1625/2077 | 1513/1650 | 505/549 | chr17 | 38182111 | ||
| chr17:38182123
|
G | A | 1 | a0020 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.1501C>T | p.Arg501Trp | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 14/14 | 1613/2077 | 1501/1650 | 501/549 | chr17 | 38182123 | ||
| chr17:38182143
|
T | C | 1 | a0011 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.1481A>G | p.Gln494Arg | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 14/14 | 1593/2077 | 1481/1650 | 494/549 | chr17 | 38182143 | ||
| chr17:38182173
|
G | T | 2 | a0004a0018 | 7 | HG01070.hp1 HG01070.hp2 HG02027.hp2 others(4): Show |
missense_variant | MODERATE | c.1451C>A | p.Ser484Tyr | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 14/14 | 1563/2077 | 1451/1650 | 484/549 | chr17 | 38182173 | ||
| chr17:38182185
|
A | G | 2 | a0004a0018 | 7 | HG01070.hp1 HG01070.hp2 HG02027.hp2 others(4): Show |
missense_variant | MODERATE | c.1439T>C | p.Val480Ala | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 14/14 | 1551/2077 | 1439/1650 | 480/549 | chr17 | 38182185 | ||
| chr17:38182300
|
C | T | 1 | a0013 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.1324G>A | p.Gly442Arg | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 14/14 | 1436/2077 | 1324/1650 | 442/549 | chr17 | 38182300 | ||
| chr17:38182359
|
C | T | 1 | a0015 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.1265G>A | p.Arg422Gln | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 14/14 | 1377/2077 | 1265/1650 | 422/549 | chr17 | 38182359 | ||
| chr17:38182407
|
G | A | 3 | a0004a0014a0018 | 8 | HG01070.hp1 HG01070.hp2 HG02027.hp2 others(5): Show |
missense_variant | MODERATE | c.1217C>T | p.Pro406Leu | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 14/14 | 1329/2077 | 1217/1650 | 406/549 | chr17 | 38182407 | ||
| chr17:38182418
|
C | T | 1 | a0022 | 1 | NA19084.hp2 | stop_gained | HIGH | c.1206G>A | p.Trp402* | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 14/14 | 1318/2077 | 1206/1650 | 402/549 | chr17 | 38182418 | ||
| chr17:38182438
|
G | A | 1 | a0012 | 1 | NA18747.hp1 | missense_variant | MODERATE | c.1186C>T | p.Arg396Trp | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 14/14 | 1298/2077 | 1186/1650 | 396/549 | chr17 | 38182438 | ||
| chr17:38183532
|
G | T | 5 | a0001a0009a0010others(2): Show | 22 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(19): Show |
missense_variant | MODERATE | c.1073C>A | p.Pro358Gln | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 13/14 | 1185/2077 | 1073/1650 | 358/549 | chr17 | 38183532 | ||
| chr17:38183545
|
T | G | 17 | a0001a0003a0007others(14): Show | 43 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(40): Show |
missense_variant | MODERATE | c.1060A>C | p.Lys354Gln | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 13/14 | 1172/2077 | 1060/1650 | 354/549 | chr17 | 38183545 | ||
| chr17:38183568
|
G | C | 1 | a0008 | 2 | HG02809.hp2 HG03579.hp1 |
missense_variant | MODERATE | c.1037C>G | p.Ser346Cys | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 13/14 | 1149/2077 | 1037/1650 | 346/549 | chr17 | 38183568 | ||
| chr17:38183597
|
C | A | 1 | a0012 | 1 | NA18747.hp1 | missense_variant | MODERATE | c.1008G>T | p.Glu336Asp | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 13/14 | 1120/2077 | 1008/1650 | 336/549 | chr17 | 38183597 | ||
| chr17:38185080
|
G | A | 1 | a0012 | 1 | NA18747.hp1 | missense_variant | MODERATE | c.742C>T | p.Pro248Ser | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 10/14 | 854/2077 | 742/1650 | 248/549 | chr17 | 38185080 | ||
| chr17:38185121
|
C | T | 1 | a0008 | 2 | HG02809.hp2 HG03579.hp1 |
missense_variant | MODERATE | c.701G>A | p.Gly234Glu | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 10/14 | 813/2077 | 701/1650 | 234/549 | chr17 | 38185121 | ||
| chr17:38187860
|
T | C | 2 | a0011a0012 | 2 | HG03453.hp1 NA18747.hp1 |
missense_variant | MODERATE | c.471A>G | p.Ile157Met | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 7/14 | 583/2077 | 471/1650 | 157/549 | chr17 | 38187860 | ||
| chr17:38187886
|
C | T | 2 | a0011a0012 | 2 | HG03453.hp1 NA18747.hp1 |
missense_variant | MODERATE | c.445G>A | p.Val149Ile | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 7/14 | 557/2077 | 445/1650 | 149/549 | chr17 | 38187886 | ||
| chr17:38187921
|
C | T | 2 | a0005a0017 | 6 | HG00438.hp2 HG01099.hp2 HG02027.hp1 others(3): Show |
missense_variant | MODERATE | c.410G>A | p.Arg137Lys | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 7/14 | 522/2077 | 410/1650 | 137/549 | chr17 | 38187921 | ||
| chr17:38188296
|
A | T | 1 | a0023 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.364T>A | p.Leu122Met | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 6/14 | 476/2077 | 364/1650 | 122/549 | chr17 | 38188296 | ||
| chr17:38188310
|
G | A | 10 | a0002a0004a0007others(7): Show | 27 | HG01070.hp2 HG01261.hp1 HG01358.hp1 others(24): Show |
missense_variant | MODERATE | c.350C>T | p.Thr117Ile | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 6/14 | 462/2077 | 350/1650 | 117/549 | chr17 | 38188310 | ||
| chr17:38188898
|
G | A | 1 | a0024 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.205C>T | p.Arg69Trp | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 5/14 | 317/2077 | 205/1650 | 69/549 | chr17 | 38188898 | ||
| chr17:38190981
|
C | G | 1 | a0025 | 1 | HG01071.hp1 | missense_variant | MODERATE | c.49G>C | p.Asp17His | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 2/14 | 161/2077 | 49/1650 | 17/549 | chr17 | 38190981 | ||
| chr17:38191023
|
C | T | 1 | a0010 | 1 | HG00597.hp1 | missense_variant | MODERATE | c.7G>A | p.Val3Met | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 2/14 | 119/2077 | 7/1650 | 3/549 | chr17 | 38191023 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:38182199
|
C | T | 29 | a0001c0001a0002c0002a0002c0023others(26): Show | 70 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(67): Show |
synonymous_variant | LOW | c.1425G>A | p.Arg475Arg | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 14/14 | 1537/2077 | 1425/1650 | 475/549 | chr17 | 38182199 | ||
| chr17:38183660
|
C | T | 1 | a0011c0022 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.945G>A | p.Thr315Thr | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 13/14 | 1057/2077 | 945/1650 | 315/549 | chr17 | 38183660 | ||
| chr17:38184086
|
A | G | 7 | a0002c0023a0004c0003a0005c0004others(4): Show | 16 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(13): Show |
synonymous_variant | LOW | c.889T>C | p.Leu297Leu | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 12/14 | 1001/2077 | 889/1650 | 297/549 | chr17 | 38184086 | ||
| chr17:38186538
|
G | A | 13 | a0001c0001a0002c0002a0003c0005others(10): Show | 41 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(38): Show |
synonymous_variant | LOW | c.540C>T | p.Tyr180Tyr | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 8/14 | 652/2077 | 540/1650 | 180/549 | chr17 | 38186538 | ||
| chr17:38187874
|
A | G | 2 | a0003c0006a0007c0010 | 4 | HG01361.hp1 HG01361.hp2 HG02818.hp2 others(1): Show |
synonymous_variant | LOW | c.457T>C | p.Leu153Leu | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 7/14 | 569/2077 | 457/1650 | 153/549 | chr17 | 38187874 | ||
| chr17:38190718
|
C | A | 1 | a0012c0029 | 1 | NA18747.hp1 | synonymous_variant | LOW | c.150G>T | p.Gly50Gly | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 3/14 | 262/2077 | 150/1650 | 50/549 | chr17 | 38190718 | ||
| chr17:38190730
|
G | A | 1 | a0014c0030 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.138C>T | p.Val46Val | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 3/14 | 250/2077 | 138/1650 | 46/549 | chr17 | 38190730 | ||
| chr17:38191006
|
G | A | 1 | a0025c0031 | 1 | HG01071.hp1 | synonymous_variant | LOW | c.24C>T | p.Gly8Gly | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 2/14 | 136/2077 | 24/1650 | 8/549 | chr17 | 38191006 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:38181785
|
G | C | 3 | a0006c0008t0005a0008c0011t0003a0021c0019t0008 | 5 | HG02717.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*189C>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 14/14 | 189 | chr17 | 38181785 | |||||
| chr17:38181793
|
T | C | 10 | a0003c0006t0004a0003c0007t0002a0005c0004t0002others(7): Show | 14 | HG01099.hp1 HG01361.hp1 HG01361.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*181A>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 14/14 | 181 | chr17 | 38181793 | |||||
| chr17:38181850
|
C | T | 1 | a0003c0006t0004 | 2 | HG01361.hp1 HG01361.hp2 |
3_prime_UTR_variant | MODIFIER | c.*124G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 14/14 | 124 | chr17 | 38181850 | |||||
| chr17:38181901
|
C | T | 3 | a0008c0011t0003a0015c0024t0006a0021c0019t0008 | 4 | HG02809.hp2 HG03579.hp1 HG03579.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*73G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 14/14 | 73 | chr17 | 38181901 | |||||
| chr17:38181907
|
T | C | 1 | a0023c0013t0010 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*67A>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 14/14 | 67 | chr17 | 38181907 | |||||
| chr17:38181909
|
C | T | 1 | a0002c0023t0007 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*65G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 14/14 | 65 | chr17 | 38181909 | |||||
| chr17:38192472
|
G | T | 1 | a0008c0011t0003 | 2 | HG02809.hp2 HG03579.hp1 |
5_prime_UTR_variant | MODIFIER | c.-29C>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/14 | 1443 | chr17 | 38192472 | |||||
| chr17:38192475
|
A | G | 1 | a0015c0024t0006 | 1 | HG03579.hp2 | 5_prime_UTR_variant | MODIFIER | c.-32T>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/14 | 1446 | chr17 | 38192475 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:38182600
|
G | A | 1 | a0001c0001t0001g0052 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1082-58C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 13/13 | chr17 | 38182600 | ||||||
| chr17:38182620
|
G | A | 1 | a0023c0013t0010g0023 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1082-78C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 13/13 | chr17 | 38182620 | ||||||
| chr17:38182641
|
T | C | 1 | a0002c0002t0001g0031 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1082-99A>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 13/13 | chr17 | 38182641 | ||||||
| chr17:38182710
|
A | G | 51 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(48): Show | 56 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1082-168T>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 13/13 | chr17 | 38182710 | ||||||
| chr17:38183026
|
GGCCCGGG others(11): Show |
G | 8 | a0003c0005t0001g0003a0003c0006t0004g0012a0003c0006t0004g0013others(5): Show | 9 | HG01071.hp1 HG01361.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.1081+480_1082-485d others(20): Show |
TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 13/13 | chr17 | 38183026 | ||||||
| chr17:38183284
|
C | A | 2 | a0011c0022t0001g0021a0023c0013t0010g0023 | 2 | HG03453.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1081+240G>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 13/13 | chr17 | 38183284 | ||||||
| chr17:38183313
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1081+211A>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 13/13 | chr17 | 38183313 | ||||||
| chr17:38183333
|
C | T | 1 | a0007c0010t0002g0015 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1081+191G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 13/13 | chr17 | 38183333 | ||||||
| chr17:38183474
|
C | T | 1 | a0021c0019t0008g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1081+50G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 13/13 | chr17 | 38183474 | ||||||
| chr17:38183514
|
T | C | 1 | a0007c0010t0002g0015 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1081+10A>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 13/13 | chr17 | 38183514 | ||||||
| chr17:38183519
|
C | G | 1 | a0017c0014t0002g0046 | 1 | HG02818.hp1 | splice_region_variant&intron_variant | LOW | c.1081+5G>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 13/13 | chr17 | 38183519 | ||||||
| chr17:38183735
|
C | T | 3 | a0003c0005t0001g0003a0011c0022t0001g0021a0023c0013t0010g0023 | 4 | HG02451.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.929-59G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 12/13 | chr17 | 38183735 | ||||||
| chr17:38183805
|
T | C | 42 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(39): Show | 47 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.929-129A>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 12/13 | chr17 | 38183805 | ||||||
| chr17:38183862
|
C | T | 3 | a0008c0011t0003g0005a0008c0011t0003g0006a0016c0026t0002g0011 | 3 | HG02809.hp2 HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.928+185G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 12/13 | chr17 | 38183862 | ||||||
| chr17:38183865
|
C | T | 3 | a0008c0011t0003g0005a0008c0011t0003g0006a0016c0026t0002g0011 | 3 | HG02809.hp2 HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.928+182G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 12/13 | chr17 | 38183865 | ||||||
| chr17:38183872
|
C | T | 1 | a0003c0005t0001g0033 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.928+175G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 12/13 | chr17 | 38183872 | ||||||
| chr17:38183884
|
G | A | 1 | a0012c0029t0009g0019 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.928+163C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 12/13 | chr17 | 38183884 | ||||||
| chr17:38183929
|
A | G | 3 | a0003c0005t0001g0003a0012c0029t0009g0019a0025c0031t0001g0024 | 4 | HG01071.hp1 HG02451.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.928+118T>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 12/13 | chr17 | 38183929 | ||||||
| chr17:38183953
|
A | C | 3 | a0003c0005t0001g0003a0011c0022t0001g0021a0012c0029t0009g0019 | 4 | HG02451.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.928+94T>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 12/13 | chr17 | 38183953 | ||||||
| chr17:38184036
|
C | T | 4 | a0008c0011t0003g0005a0008c0011t0003g0006a0015c0024t0006g0004others(1): Show | 4 | HG02809.hp2 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.928+11G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 12/13 | chr17 | 38184036 | ||||||
| chr17:38184278
|
C | T | 1 | a0007c0010t0002g0015 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.829-132G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 11/13 | chr17 | 38184278 | ||||||
| chr17:38184323
|
T | C | 2 | a0005c0004t0001g0045a0007c0010t0002g0035 | 2 | NA18950.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.829-177A>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 11/13 | chr17 | 38184323 | ||||||
| chr17:38184444
|
G | T | 1 | a0012c0029t0009g0019 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.828+166C>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 11/13 | chr17 | 38184444 | ||||||
| chr17:38184461
|
C | T | 1 | a0012c0029t0009g0019 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.828+149G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 11/13 | chr17 | 38184461 | ||||||
| chr17:38184749
|
C | G | 1 | a0015c0024t0006g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.763-74G>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 10/13 | chr17 | 38184749 | ||||||
| chr17:38184850
|
C | T | 12 | a0002c0002t0001g0007a0002c0002t0001g0020a0002c0002t0001g0025others(9): Show | 12 | HG01261.hp1 HG01358.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.763-175G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 10/13 | chr17 | 38184850 | ||||||
| chr17:38184943
|
A | G | 7 | a0004c0003t0001g0038a0005c0004t0001g0042a0005c0004t0001g0043others(4): Show | 7 | HG01099.hp2 HG02027.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.762+117T>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 10/13 | chr17 | 38184943 | ||||||
| chr17:38184946
|
C | A | 11 | a0002c0002t0001g0007a0002c0002t0001g0020a0002c0002t0001g0025others(8): Show | 11 | HG01261.hp1 HG01358.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.762+114G>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 10/13 | chr17 | 38184946 | ||||||
| chr17:38184987
|
T | C | 1 | a0012c0029t0009g0019 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.762+73A>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 10/13 | chr17 | 38184987 | ||||||
| chr17:38185009
|
T | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(61): Show | 70 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.762+51A>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 10/13 | chr17 | 38185009 | ||||||
| chr17:38185218
|
T | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(61): Show | 70 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.668-64A>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 9/13 | chr17 | 38185218 | ||||||
| chr17:38185271
|
A | G | 15 | a0002c0023t0007g0036a0004c0003t0001g0018a0004c0003t0001g0037others(12): Show | 15 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.668-117T>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 9/13 | chr17 | 38185271 | ||||||
| chr17:38185301
|
C | T | 1 | a0003c0007t0002g0002 | 2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.668-147G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 9/13 | chr17 | 38185301 | ||||||
| chr17:38185403
|
C | T | 1 | a0005c0004t0001g0042 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.668-249G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 9/13 | chr17 | 38185403 | ||||||
| chr17:38185426
|
G | A | 2 | a0003c0006t0004g0012a0003c0006t0004g0013 | 2 | HG01361.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.668-272C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 9/13 | chr17 | 38185426 | ||||||
| chr17:38185470
|
A | G | 30 | a0001c0001t0001g0059a0001c0001t0001g0062a0002c0002t0001g0007others(27): Show | 30 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.668-316T>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 9/13 | chr17 | 38185470 | ||||||
| chr17:38185511
|
C | G | 1 | a0011c0022t0001g0021 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.667+357G>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 9/13 | chr17 | 38185511 | ||||||
| chr17:38185517
|
G | A | 41 | a0001c0001t0001g0059a0001c0001t0001g0062a0002c0002t0001g0007others(38): Show | 43 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.667+351C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 9/13 | chr17 | 38185517 | ||||||
| chr17:38185542
|
A | G | 1 | a0003c0007t0002g0002 | 2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.667+326T>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 9/13 | chr17 | 38185542 | ||||||
| chr17:38185546
|
C | T | 1 | a0023c0013t0010g0023 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.667+322G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 9/13 | chr17 | 38185546 | ||||||
| chr17:38185547
|
G | A | 1 | a0016c0026t0002g0011 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.667+321C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 9/13 | chr17 | 38185547 | ||||||
| chr17:38185606
|
G | C | 1 | a0001c0001t0001g0057 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.667+262C>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 9/13 | chr17 | 38185606 | ||||||
| chr17:38185643
|
C | T | 2 | a0003c0005t0001g0003a0025c0031t0001g0024 | 3 | HG01071.hp1 HG02451.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.667+225G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 9/13 | chr17 | 38185643 | ||||||
| chr17:38185679
|
G | C | 24 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0058others(21): Show | 25 | HG00741.hp1 HG00741.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.667+189C>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 9/13 | chr17 | 38185679 | ||||||
| chr17:38185683
|
C | G | 2 | a0008c0011t0003g0005a0008c0011t0003g0006 | 2 | HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.667+185G>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 9/13 | chr17 | 38185683 | ||||||
| chr17:38185684
|
G | A | 1 | a0004c0003t0001g0039 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.667+184C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 9/13 | chr17 | 38185684 | ||||||
| chr17:38185709
|
C | T | 1 | a0004c0003t0001g0039 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.667+159G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 9/13 | chr17 | 38185709 | ||||||
| chr17:38185743
|
C | T | 4 | a0003c0005t0001g0003a0006c0008t0005g0016a0021c0019t0008g0017others(1): Show | 5 | HG02451.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.667+125G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 9/13 | chr17 | 38185743 | ||||||
| chr17:38185806
|
T | C | 7 | a0008c0011t0003g0005a0008c0011t0003g0006a0011c0022t0001g0021others(4): Show | 7 | HG01071.hp1 HG02809.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.667+62A>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 9/13 | chr17 | 38185806 | ||||||
| chr17:38186018
|
C | T | 1 | a0003c0005t0001g0003 | 2 | HG02451.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.547-30G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 8/13 | chr17 | 38186018 | ||||||
| chr17:38186044
|
C | T | 62 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(59): Show | 68 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.547-56G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 8/13 | chr17 | 38186044 | ||||||
| chr17:38186045
|
G | T | 1 | a0007c0010t0002g0015 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.547-57C>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 8/13 | chr17 | 38186045 | ||||||
| chr17:38186258
|
CAGG | C | 6 | a0001c0001t0001g0049a0001c0001t0001g0059a0001c0001t0001g0060others(3): Show | 6 | HG01358.hp2 HG02129.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.546+271_547-271del others(3): Show |
TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 8/13 | chr17 | 38186258 | ||||||
| chr17:38186323
|
A | C | 1 | a0023c0013t0010g0023 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.546+209T>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 8/13 | chr17 | 38186323 | ||||||
| chr17:38186323
|
A | G | 2 | a0011c0022t0001g0021a0012c0029t0009g0019 | 2 | HG03453.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.546+209T>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 8/13 | chr17 | 38186323 | ||||||
| chr17:38186324
|
G | A | 1 | a0023c0013t0010g0023 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.546+208C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 8/13 | chr17 | 38186324 | ||||||
| chr17:38186337
|
T | C | 11 | a0002c0023t0007g0036a0003c0006t0004g0012a0003c0006t0004g0013others(8): Show | 12 | HG01070.hp1 HG01070.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.546+195A>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 8/13 | chr17 | 38186337 | ||||||
| chr17:38186367
|
C | T | 4 | a0008c0011t0003g0005a0008c0011t0003g0006a0015c0024t0006g0004others(1): Show | 4 | HG02809.hp2 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.546+165G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 8/13 | chr17 | 38186367 | ||||||
| chr17:38186444
|
T | G | 19 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(16): Show | 23 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.546+88A>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 8/13 | chr17 | 38186444 | ||||||
| chr17:38186505
|
G | A | 1 | a0008c0011t0003g0006 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.546+27C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 8/13 | chr17 | 38186505 | ||||||
| chr17:38186594
|
A | G | 1 | a0023c0013t0010g0023 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.498-14T>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 7/13 | chr17 | 38186594 | ||||||
| chr17:38186681
|
T | G | 5 | a0008c0011t0003g0005a0008c0011t0003g0006a0014c0030t0001g0029others(2): Show | 5 | HG02451.hp1 HG02809.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.498-101A>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 7/13 | chr17 | 38186681 | ||||||
| chr17:38186722
|
T | C | 7 | a0005c0004t0001g0042a0005c0004t0001g0043a0005c0004t0001g0045others(4): Show | 7 | HG00438.hp2 HG01070.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.498-142A>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 7/13 | chr17 | 38186722 | ||||||
| chr17:38186813
|
A | AT | 11 | a0003c0006t0004g0012a0003c0006t0004g0013a0004c0003t0001g0039others(8): Show | 11 | HG01071.hp1 HG01361.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.498-234dupA | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 7/13 | chr17 | 38186813 | ||||||
| chr17:38186813
|
A | ATT | 13 | a0002c0023t0007g0036a0004c0003t0001g0037a0004c0003t0001g0038others(10): Show | 13 | HG00438.hp2 HG01070.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.498-235_498-234dup others(2): Show |
TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 7/13 | chr17 | 38186813 | ||||||
| chr17:38186813
|
ATTTTT | A | 25 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(22): Show | 31 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.498-238_498-234del others(5): Show |
TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 7/13 | chr17 | 38186813 | ||||||
| chr17:38186838
|
T | C | 63 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(60): Show | 69 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.498-258A>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 7/13 | chr17 | 38186838 | ||||||
| chr17:38186888
|
A | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(45): Show | 54 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.498-308T>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 7/13 | chr17 | 38186888 | ||||||
| chr17:38186899
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.498-319A>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 7/13 | chr17 | 38186899 | ||||||
| chr17:38186973
|
C | A | 3 | a0003c0005t0001g0003a0011c0022t0001g0021a0023c0013t0010g0023 | 4 | HG02451.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.498-393G>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 7/13 | chr17 | 38186973 | ||||||
| chr17:38186999
|
T | C | 63 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(60): Show | 69 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.498-419A>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 7/13 | chr17 | 38186999 | ||||||
| chr17:38187003
|
G | A | 1 | a0015c0024t0006g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.498-423C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 7/13 | chr17 | 38187003 | ||||||
| chr17:38187073
|
G | T | 32 | a0002c0023t0007g0036a0003c0005t0001g0003a0003c0006t0004g0012others(29): Show | 34 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.498-493C>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 7/13 | chr17 | 38187073 | ||||||
| chr17:38187129
|
C | A | 1 | a0012c0029t0009g0019 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.498-549G>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 7/13 | chr17 | 38187129 | ||||||
| chr17:38187167
|
C | G | 2 | a0003c0006t0004g0012a0003c0006t0004g0013 | 2 | HG01361.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.498-587G>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 7/13 | chr17 | 38187167 | ||||||
| chr17:38187177
|
C | T | 1 | a0015c0024t0006g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.498-597G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 7/13 | chr17 | 38187177 | ||||||
| chr17:38187231
|
G | A | 1 | a0005c0004t0001g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.497+603C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 7/13 | chr17 | 38187231 | ||||||
| chr17:38187353
|
G | C | 1 | a0011c0022t0001g0021 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.497+481C>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 7/13 | chr17 | 38187353 | ||||||
| chr17:38187391
|
G | T | 2 | a0011c0022t0001g0021a0012c0029t0009g0019 | 2 | HG03453.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.497+443C>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 7/13 | chr17 | 38187391 | ||||||
| chr17:38187494
|
GC | G | 1 | a0003c0005t0001g0003 | 2 | HG02451.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.497+339delG | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 7/13 | chr17 | 38187494 | ||||||
| chr17:38187495
|
C | G | 38 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(35): Show | 42 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.497+339G>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 7/13 | chr17 | 38187495 | ||||||
| chr17:38187498
|
G | T | 17 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(14): Show | 21 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.497+336C>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 7/13 | chr17 | 38187498 | ||||||
| chr17:38187531
|
G | A | 6 | a0005c0004t0001g0042a0005c0004t0001g0045a0005c0004t0001g0066others(3): Show | 6 | HG00438.hp2 HG01070.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.497+303C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 7/13 | chr17 | 38187531 | ||||||
| chr17:38187694
|
G | A | 2 | a0008c0011t0003g0005a0008c0011t0003g0006 | 2 | HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.497+140C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 7/13 | chr17 | 38187694 | ||||||
| chr17:38187824
|
G | A | 2 | a0011c0022t0001g0021a0012c0029t0009g0019 | 2 | HG03453.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.497+10C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 7/13 | chr17 | 38187824 | ||||||
| chr17:38188033
|
C | T | 4 | a0008c0011t0003g0005a0008c0011t0003g0006a0015c0024t0006g0004others(1): Show | 4 | HG02809.hp2 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.388-90G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 6/13 | chr17 | 38188033 | ||||||
| chr17:38188229
|
C | A | 1 | a0023c0013t0010g0023 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.387+44G>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 6/13 | chr17 | 38188229 | ||||||
| chr17:38188385
|
G | A | 1 | a0023c0013t0010g0023 | 1 | HG04228.hp2 | splice_region_variant&intron_variant | LOW | c.280-5C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 5/13 | chr17 | 38188385 | ||||||
| chr17:38188396
|
G | A | 1 | a0023c0013t0010g0023 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.280-16C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 5/13 | chr17 | 38188396 | ||||||
| chr17:38188487
|
T | G | 1 | a0003c0005t0001g0033 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.280-107A>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 5/13 | chr17 | 38188487 | ||||||
| chr17:38188517
|
C | T | 1 | a0005c0004t0001g0042 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.280-137G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 5/13 | chr17 | 38188517 | ||||||
| chr17:38188550
|
C | G | 2 | a0003c0006t0004g0012a0003c0006t0004g0013 | 2 | HG01361.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.280-170G>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 5/13 | chr17 | 38188550 | ||||||
| chr17:38188593
|
C | A | 60 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(57): Show | 66 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.280-213G>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 5/13 | chr17 | 38188593 | ||||||
| chr17:38189042
|
G | A | 1 | a0002c0002t0001g0020 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.199-138C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 4/13 | chr17 | 38189042 | ||||||
| chr17:38189160
|
G | A | 1 | a0021c0019t0008g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.198+227C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 4/13 | chr17 | 38189160 | ||||||
| chr17:38189202
|
A | G | 1 | a0012c0029t0009g0019 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.198+185T>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 4/13 | chr17 | 38189202 | ||||||
| chr17:38189278
|
G | T | 1 | a0025c0031t0001g0024 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.198+109C>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 4/13 | chr17 | 38189278 | ||||||
| chr17:38189293
|
G | A | 2 | a0011c0022t0001g0021a0012c0029t0009g0019 | 2 | HG03453.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.198+94C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 4/13 | chr17 | 38189293 | ||||||
| chr17:38189361
|
A | T | 1 | a0002c0002t0001g0032 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.198+26T>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 4/13 | chr17 | 38189361 | ||||||
| chr17:38189601
|
G | C | 17 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0052others(14): Show | 21 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.159-175C>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 3/13 | chr17 | 38189601 | ||||||
| chr17:38189601
|
G | T | 1 | a0001c0001t0001g0051 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.159-175C>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 3/13 | chr17 | 38189601 | ||||||
| chr17:38189644
|
G | A | 1 | a0023c0013t0010g0023 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.159-218C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 3/13 | chr17 | 38189644 | ||||||
| chr17:38189665
|
G | A | 1 | a0012c0029t0009g0019 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.159-239C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 3/13 | chr17 | 38189665 | ||||||
| chr17:38189674
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.159-248C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 3/13 | chr17 | 38189674 | ||||||
| chr17:38189688
|
A | G | 1 | a0003c0006t0004g0012 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.159-262T>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 3/13 | chr17 | 38189688 | ||||||
| chr17:38189700
|
G | C | 7 | a0002c0002t0001g0007a0002c0002t0001g0020a0002c0002t0001g0025others(4): Show | 7 | HG02273.hp1 HG02273.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.159-274C>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 3/13 | chr17 | 38189700 | ||||||
| chr17:38189862
|
G | A | 1 | a0014c0030t0001g0029 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.159-436C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 3/13 | chr17 | 38189862 | ||||||
| chr17:38189891
|
C | A | 1 | a0011c0022t0001g0021 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.159-465G>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 3/13 | chr17 | 38189891 | ||||||
| chr17:38189900
|
C | T | 6 | a0002c0002t0001g0007a0002c0002t0001g0020a0002c0002t0001g0025others(3): Show | 6 | HG02273.hp1 HG02273.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.159-474G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 3/13 | chr17 | 38189900 | ||||||
| chr17:38189919
|
G | A | 1 | a0025c0031t0001g0024 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.159-493C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 3/13 | chr17 | 38189919 | ||||||
| chr17:38189961
|
A | G | 2 | a0001c0001t0001g0050a0002c0002t0001g0032 | 2 | HG01071.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.159-535T>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 3/13 | chr17 | 38189961 | ||||||
| chr17:38189971
|
C | T | 1 | a0015c0024t0006g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.159-545G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 3/13 | chr17 | 38189971 | ||||||
| chr17:38189992
|
G | C | 1 | a0023c0013t0010g0023 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.159-566C>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 3/13 | chr17 | 38189992 | ||||||
| chr17:38189997
|
G | T | 3 | a0008c0011t0003g0005a0008c0011t0003g0006a0015c0024t0006g0004 | 3 | HG02809.hp2 HG03579.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.159-571C>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 3/13 | chr17 | 38189997 | ||||||
| chr17:38190069
|
C | T | 1 | a0023c0013t0010g0023 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.158+641G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 3/13 | chr17 | 38190069 | ||||||
| chr17:38190090
|
C | T | 1 | a0012c0029t0009g0019 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.158+620G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 3/13 | chr17 | 38190090 | ||||||
| chr17:38190195
|
CT | C | 3 | a0008c0011t0003g0005a0008c0011t0003g0006a0015c0024t0006g0004 | 3 | HG02809.hp2 HG03579.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.158+514delA | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 3/13 | chr17 | 38190195 | ||||||
| chr17:38190267
|
T | C | 1 | a0014c0030t0001g0029 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.158+443A>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 3/13 | chr17 | 38190267 | ||||||
| chr17:38190322
|
C | G | 64 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(61): Show | 70 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.158+388G>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 3/13 | chr17 | 38190322 | ||||||
| chr17:38190348
|
A | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(61): Show | 70 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.158+362T>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 3/13 | chr17 | 38190348 | ||||||
| chr17:38190390
|
T | G | 63 | a0001c0001t0001g0001a0001c0001t0001g0050a0001c0001t0001g0051others(60): Show | 69 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.158+320A>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 3/13 | chr17 | 38190390 | ||||||
| chr17:38190509
|
C | T | 4 | a0002c0002t0001g0020a0002c0002t0001g0025a0013c0027t0001g0022others(1): Show | 4 | HG02451.hp1 HG02738.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.158+201G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 3/13 | chr17 | 38190509 | ||||||
| chr17:38190579
|
T | C | 1 | a0004c0003t0001g0018 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.158+131A>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 3/13 | chr17 | 38190579 | ||||||
| chr17:38190628
|
G | A | 1 | a0003c0005t0001g0003 | 2 | HG02451.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.158+82C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 3/13 | chr17 | 38190628 | ||||||
| chr17:38190682
|
AG | A | 3 | a0004c0003t0001g0041a0017c0014t0002g0046a0021c0019t0008g0017 | 3 | HG02818.hp1 NA18950.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.158+27delC | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 3/13 | chr17 | 38190682 | ||||||
| chr17:38190683
|
G | A | 1 | a0007c0010t0002g0015 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.158+27C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 3/13 | chr17 | 38190683 | ||||||
| chr17:38190908
|
C | G | 1 | a0012c0029t0009g0019 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.72+50G>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 2/13 | chr17 | 38190908 | ||||||
| chr17:38191061
|
C | T | 21 | a0002c0002t0001g0020a0002c0002t0001g0025a0002c0002t0001g0026others(18): Show | 23 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.-1-31G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/13 | chr17 | 38191061 | ||||||
| chr17:38191068
|
G | C | 1 | a0023c0013t0010g0023 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-1-38C>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/13 | chr17 | 38191068 | ||||||
| chr17:38191102
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-1-72C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/13 | chr17 | 38191102 | ||||||
| chr17:38191158
|
A | C | 2 | a0008c0011t0003g0005a0008c0011t0003g0006 | 2 | HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-1-128T>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/13 | chr17 | 38191158 | ||||||
| chr17:38191182
|
A | G | 1 | a0003c0005t0001g0003 | 2 | HG02451.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-1-152T>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/13 | chr17 | 38191182 | ||||||
| chr17:38191229
|
A | G | 8 | a0002c0002t0001g0032a0003c0005t0001g0003a0003c0006t0004g0012others(5): Show | 9 | HG01361.hp1 HG01361.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1-199T>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/13 | chr17 | 38191229 | ||||||
| chr17:38191308
|
T | C | 66 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(63): Show | 72 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.-1-278A>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/13 | chr17 | 38191308 | ||||||
| chr17:38191397
|
G | A | 1 | a0006c0008t0005g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-1-367C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/13 | chr17 | 38191397 | ||||||
| chr17:38191443
|
C | G | 1 | a0025c0031t0001g0024 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-1-413G>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/13 | chr17 | 38191443 | ||||||
| chr17:38191448
|
C | A | 1 | a0025c0031t0001g0024 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-1-418G>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/13 | chr17 | 38191448 | ||||||
| chr17:38191484
|
C | T | 2 | a0003c0006t0004g0012a0003c0006t0004g0013 | 2 | HG01361.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.-1-454G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/13 | chr17 | 38191484 | ||||||
| chr17:38191595
|
G | A | 1 | a0025c0031t0001g0024 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-1-565C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/13 | chr17 | 38191595 | ||||||
| chr17:38191603
|
A | G | 43 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(40): Show | 49 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.-1-573T>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/13 | chr17 | 38191603 | ||||||
| chr17:38191670
|
C | A | 1 | a0015c0024t0006g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-1-640G>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/13 | chr17 | 38191670 | ||||||
| chr17:38191671
|
G | A | 1 | a0002c0002t0001g0032 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-1-641C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/13 | chr17 | 38191671 | ||||||
| chr17:38191736
|
G | A | 20 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(17): Show | 24 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.-1-706C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/13 | chr17 | 38191736 | ||||||
| chr17:38191795
|
C | T | 21 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(18): Show | 25 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.-2+650G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/13 | chr17 | 38191795 | ||||||
| chr17:38191916
|
G | C | 1 | a0017c0014t0002g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-2+529C>G | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/13 | chr17 | 38191916 | ||||||
| chr17:38191919
|
GCCCAAGG others(11): Show |
G | 1 | a0021c0019t0008g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-2+508_-2+525delGA others(16): Show |
TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/13 | chr17 | 38191919 | ||||||
| chr17:38192024
|
T | TCAGTGGA others(7): Show |
55 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(52): Show | 60 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.-2+420_-2+421insGT others(12): Show |
TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/13 | chr17 | 38192024 | ||||||
| chr17:38192031
|
C | A | 8 | a0003c0006t0004g0012a0003c0006t0004g0013a0003c0007t0002g0002others(5): Show | 9 | HG01361.hp1 HG01361.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-2+414G>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/13 | chr17 | 38192031 | ||||||
| chr17:38192035
|
G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(52): Show | 60 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.-2+410C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/13 | chr17 | 38192035 | ||||||
| chr17:38192058
|
A | G | 1 | a0003c0007t0002g0002 | 2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-2+387T>C | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/13 | chr17 | 38192058 | ||||||
| chr17:38192059
|
G | A | 1 | a0003c0005t0001g0033 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-2+386C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/13 | chr17 | 38192059 | ||||||
| chr17:38192177
|
G | A | 14 | a0002c0023t0007g0036a0004c0003t0001g0037a0004c0003t0001g0038others(11): Show | 14 | HG00438.hp2 HG01070.hp1 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.-2+268C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/13 | chr17 | 38192177 | ||||||
| chr17:38192186
|
G | A | 3 | a0007c0025t0002g0047a0008c0011t0003g0005a0008c0011t0003g0006 | 3 | HG02809.hp2 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-2+259C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/13 | chr17 | 38192186 | ||||||
| chr17:38192236
|
G | A | 1 | a0015c0024t0006g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-2+209C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/13 | chr17 | 38192236 | ||||||
| chr17:38192286
|
C | T | 1 | a0002c0002t0001g0007 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-2+159G>A | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/13 | chr17 | 38192286 | ||||||
| chr17:38192326
|
G | A | 19 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(16): Show | 23 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.-2+119C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/13 | chr17 | 38192326 | ||||||
| chr17:38192330
|
G | A | 1 | a0005c0004t0001g0066 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-2+115C>T | TBC1D3 | ENSG00000274611.4 | transcript | ENST00000620215.3 | protein_coding | 1/13 | chr17 | 38192330 |